NZ624493B2 - Ultra-concentrated rapid-acting insulin analogue formulations - Google Patents

Abstract

pharmaceutical formulation comprises insulin having a variant insulin B-chain polypeptide containing an monofluoro-Phenylalanine substitution at position B24 in combination with a substitution of an amino acid containing an acidic side chain at position B10, allowing the insulin to be present at a concentration of between 0.6 mM and 3.0 mM. The formulation may optionally be devoid of zinc. Amino-acid substitutions at one or more of positions B3, B28, and B29 may additionally be present. The variant B-chain polypeptide may be a portion of a proinsulin analogue or single-chain insulin analogue. The insulin analogue may be an analogue of a mammalian insulin, such as human insulin. A method of lowering the blood sugar of a patient comprises administering a physiologically effective amount of the insulin analogue or a physiologically acceptable salt thereof to the patient. concentration of between 0.6 mM and 3.0 mM. The formulation may optionally be devoid of zinc. Amino-acid substitutions at one or more of positions B3, B28, and B29 may additionally be present. The variant B-chain polypeptide may be a portion of a proinsulin analogue or single-chain insulin analogue. The insulin analogue may be an analogue of a mammalian insulin, such as human insulin. A method of lowering the blood sugar of a patient comprises administering a physiologically effective amount of the insulin analogue or a physiologically acceptable salt thereof to the patient.

Description

ULTRA—CONCENTRATED RAPID-ACTING INSULIN ANALOGUE FORMULATIONS ENT REGARDING LLY SPONSORED CH OR DEVELOPMENT This invention was made with government suppon under cooperative agreements awarded by the National Institutes of Health under grant numbers DK40949 and DK074176.

The US. government may have certain rights to the invention.

BACKGROUND OF THE INVENTION This invention relates to polypeptide hormone analogues that exhibit enhanced pharmaceutical properties, such as more rapid pharmacokinetics at polypeptide concentrations greater than are ordinarily employed in pharmaceutical ations. This invention also relates to n analogues that are modified by the incorporation of non-standard amino acids to enable their formulation at concentrations higher than 100 units per ml (U-100) such that (i) rapid-acting pharmacokinetic (PK) and pharmacodynamic (PD) properties are retained relative to ype human insulin at a U-lOO concentration and such that (ii) their mitogenic properties are not elevated relative to wild-type human insulin. Such non-standard sequences may optionally contain rd acid substitutions at other sites in the A or B chains of an insulin analogue.

The engineering of non—standard proteins, including therapeutic agents and vaccines, may have broad medical and societal benefits. An e of a medical benefit would be zation of the pharmacokinetic properties of a protein. An example of a further societal benefit would be the ering of proteins amenable to formulation at high protein trations with deterioration of the PK/PD properties of the formulation. An example of a therapeutic protein is provided by insulin. Analogues of insulin containing non—standard amino— acid substitutions may in principle exhibit superior properties with respect to PK/PD or the dependence of PK/PD on the concentration of n in the ation. The challenge posed by the pharmacokinetics of insulin absorption following subcutaneous injection affects the ability of patients with diabetes mellitus (DM) to achieve tight glycemic control and constrains the safety and performance ofinsulin pumps.

A particular l need is posed by the marked resistance to insulin exhibited by certain patients with DM associated with obesity, by certain patients with DM associated with a genetic predisposition to insulin resistance, and by patients with DM secondary to lipodystrophy, treatment with corticosteroids, or over-secretion of endogenous corticosteroids (Cushing’s Syndrome). The number of patients with marked insulin resistance is growing due to the obesity ic in the developed and developing worlds (leading to the syndrome of “diabesity”) and due to the increasing recognition of a monogenic form of DM arising from a mutation in mitochondrial DNA in which insulin resistance can be unusually severe (van den Ouweland, J.M., Lemkes, H.H., Ruitenbeek, W., Sandkuijl, L.A., de Vijlder, M.F., Struyvenberg, P.A., van de Kamp, J.J., & Maassen, J.A. (1992) Mutation in ondrial eu)(UUR) gene in a large pedigree with ally itted type II diabetes mellitus and deafness. Nature Genet. 1, 368-71). Treatment of such otherwise diverse subsets of patients typically requires the subcutaneous injection of large volumes of regular insulin formulations (U-lOO strength; ordinarily 0.6 mM insulin or insulin analogue). Injection of such large s can lead to pain and variability in the rate of onset and duration of insulin . Although a U-SOO ation of wild-type insulin is ble for clinical use (Humulin® R U-500; Eli Lilly and Co.), the se in insulin tration from 0.6 mM to 3 mM leads to a delay in the onset, and prolongation, of insulin action such that the PK/PD properties of Humulin® R U-500, or similar such products, resemble those of a micro-crystalline sion of protamine-zinc-containing insulin hexamers; this formulation has long been designated neutral ine Hagadom (NPH).

Prandial use of a U-SOO formulation of wild-type insulin by subcutaneous injection would thus be expected to decrease the efficacy of glycemic control and se the risk of hypoglycemic episodes. Use of Humulin® R U-500, or similar such products in a device for continuous subcutaneous insulin infusion (CSIl; an “insulin pump”) would likewise be expected to interfere with the ability of the patient or l algorithm to make effective adjustments in insulin infusion rates based on current or past measurements of blood glucose concentrations, leading to suboptimal glycemic control and increased risk of hypoglycemic events.

A well-established principle of insulin pharmacology relates the aggregation state of the injected insulin molecule to the time course of tion from the depot into capillaries and hence into the systemic circulation. In general the more aggregated are the insulin molecules into high-molecular weight complexes, the greater the delay in absorption and more ged the insulin action. Amino-acid substitutions in the insulin molecule that weaken its self- assembly are known in the art to be associated with more rapid absorption relative to wild-type human insulin; examples are provided by the substitution ProBngi Asp (insulin aspart, the active ent of Novolog®; Novo-Nordisk, Ltd) and by the paired substitutions Prostfi Lys and LysB2911 Pro (insulin Lispro, the active component of Humalog®; Eli Lilly and Co.). sely, amino—acid extensions or chemical modifications of the insulin le that cause a shift in its isoelectric point (pl) from ca. pH 5 to ca. pH 7 are known in the art to lead to isoelectric precipitation of the modified n in the subcutaneous depot; such high molecular—weight complexes provide prolonged absorption as a basal insulin formulation. Examples are provided by NovoSol Basal® (a discontinued product of Novo-Nordisk in which 7 was substituted by Arg and in which the C-terminal ylate moiety of Thr1330 was amidated) and insulin glargz'ne (the active component of Lantus®, a basal formulation in which the B chain was extended by the dipeptide ArgB3l-ArgB32; Sanofi-Aventis, Ltd.). (NovoSol Basal® and Lantus® each contain the additional substitution fi Gly to enable their soluble formulation under acidic conditions (pH 3 and pH 4 respectively) without chemical degradation due to deamidation of AsnAZl.) Prolongation of cal micro-crystalline insulin suspensions (NPH, semi-lente, lente, and ultra-lente) exhibit a range of intermediate-to-long—acting PK/PD properties reflecting the respective o-chemical properties of these micro-crystals and their ve rates of dissolution.

The above insulin products, including current and past formulations of wild-type human insulin or animal insulins, employ or employed self-assembly of the insulin molecule as a means to achieve chemical stability, as a means to avoid fibril formation, as a means to modulate PK/PD properties, or as a means to achieve a ation of these objectives. Yet insulin self- assembly can also introduce unfavorable 0r undesired properties. The non-optimal prolonged PK/PD properties of Humulin® R U-500 (or a similar such product), for example, are likely to be the result of hexamer-hexamer ations in the formulation and in the subcutaneous depot.

Indeed, studies of wild-type bovine insulin zinc hexamers in Vitro by laser light scattering have provided evidence of ssive hexamer—hexamer interactions in the tration range 0.3—3 mM. Current and past strategies for the composition of insulin formulations and design of insulin analogues therefore face and have faced an irreconcilable barrier to the development of a rapid-acting ultra-concentrated insulin formulation: whereas self-assembly is necessary to obtain chemical and physical ity, its progressive nature above 0.6 mM leads to unfavorable prolongation of PK/PD.

During the past decade specific chemical modifications to the insulin molecule have been described that selectively modify one or r particular property of the protein to facilitate an application of interest. Whereas at the beginning of the recombinant DNA era (1980) wild—type human insulin was envisaged as being l for use in diverse therapeutic contexts, the broad clinical use of insulin analogues in the past decade suggests that a suite of non-standard analogs, each tailored to address a c unmet need, would provide significant medical and societal benefits. Substitution of one natural amino acid at a specific position in a protein by another natural amino acid is well known in the art and is herein designated a standard substitution. Non—standard substitutions in insulin offer the prospect of rated absorption without worsening of PIUPD as a function of insulin analogue concentration in the range 0.6 — 3.0 mM.

Administration of insulin has long been established as a treatment for diabetes mellitus. Insulin is a small globular protein that plays a central role in lism in vertebrates.

Insulin contains two chains, an A chain, containing 21 residues, and a B chain containing 30 residues. The hormone is stored in the atic b-cell as a Zn2+-stabilized hexamer, but functions as a Zn2+-free monomer in the bloodstream. Insulin is the t of a single-chain precursor, proinsulin, in which a connecting region (35 residues) links the C-terminal residue of B chain ue B30) to the inal residue of the A chain. lline arrays of zinc insulin hexamers within mature storage granules have been ized by electron microscopy (EM).

The sequence of insulin is shown in schematic form in Figure 1. Individual residues are indicated by the identity of the amino acid (typically using a standard three—letter code), the chain and sequence position (typically as a superscript).

Aromatic side chains in n, as in globular proteins in general, may engage in a variety of hydrophobic and weakly polar interactions, involving not only oring aromatic rings but also other sources of positive- or negative electrostatic potential. Examples e main—chain carbonyl- and amide groups in peptide bonds. Hydrophobic packing of aromatic side chains is believed to occur within the core of proteins and at non-polar interfaces between proteins. Such aromatic side chains can be conserved among rate ns, reflecting their key contributions to structure or function. An example of a natural aromatic amino acid is alanine. Its aromatic ring system contains six carbons arranged as a planar hexagon.

Aromaticity is a collective property of the binding arrangement among these six carbons, g to p electronic ls above and below the plane of the ring. These faces t a partial negative electrostatic potential whereas the edge of the ring, containing five C-H moieties, exhibits a partial positive electrostatic potential. This asymmetric distribution of partial charges gives rise to a quadrapole electrostatic moment and may participate in weakly polar interactions with other formal or partial charges in a n. An additional characteristic feature of an aromatic side chains is its volume. Determinants of this volume include the topographic contours of its five C—H moieties at the edges of the planar ring. Substitution of one C—H moiety by a GP moiety would be expected to preserve its aromaticity but introduced a significant dipole moment in the ring due to the electronegativity of the fluorine atom and consequent distortion of the p electronic orbitals above and below the plane of the ring. Whereas the size of the C-F moiety is similar to that of the native C—H moiety (and so could in principle be accommodated in diverse protein environments), its local onegativity and ring-specific fluorine-induced ostatic dipole moment could introduce favorable or unfavorable electrostatic interactions with neighboring groups in a protein. Examples of such neighboring groups include, but are not cted to, CO-NH e bond units, lone pair electrons of sulfur atoms in disulfide bridges, side-chain carboxamide functions (Asn and Gln), other aromatic rings (Phe, Tyr, Trp, and His), and the formal positive and ve charges of acidic side chains (Asp and Glu), basic side chains (Lys and Arg), a titratable side chain with potential pKa in the range used in insulin formations (His), titratable N— and C-terminal chain termini, bound metal ions (such as Zn2+ or Ca2+), and protein-bound water molecules.

An example of a conserved aromatic residue in a therapeutic protein is ed by phenylalanine at position B24 of the B chain ofinsulin (designated Phe ). This is one of three phenylalanine residues in insulin (positions Bl, B24, and B25). A structurally similar tyrosine is 824 - at position B26. The structural environment of Phe 1n an insulin monomer is shown in a ribbon model (Fig. 2A) and in a filling model (Fig. 2B). Conserved among vertebrate insulins and insulin—like growth factors, the aromatic ring of Phe1324 packs against (but not within) the hydrophobic core to stabilize the super-secondary structure of the B chain. Phe!324 lies at the classical receptor-binding surface and has been proposed to direct a change in mation on receptor binding. Phe1324 packs at the dimer interface of insulin and so at three interfaces of an insulin hexamer. Its structural environment in the insulin r differs from its structural environment at these interfaces. In particular, the surrounding volume available to the side chain of PheB24 is larger in the monomer than in the dimer or hexamer.

A major goal of insulin replacement therapy in patients with DM is tight control of the blood glucose tration to prevent its excursion above or below the normal range characteristic of healthy human subjects. Excursions below the normal range are associated with immediate adrenergic or neuroglycopenic symptoms, which in severe episodes lead to convulsions, coma, and death. Excursions above the normal range are associated with increased long—term risk of microvascular e, including pathy, blindness, and renal failure.

Because the pharmacokinetics of absorption of wild-type human insulin or human insulin analogues—when formulated at strengths greater than U—lOO—is often too slow, too prolonged and too variable relative to the physiological requirements of randial lic homeostasis, patients with DM associated with marked insulin resistance often fail to achieve optimal glycemic targets and are thus at increased risk of both immediate and long—term complications. Thus, the safety, efficacy, and real-world convenience of regular and rapid-acting insulin products have been limited by prolongation of PK/PD as the concentration of self- assembled insulin or insulin analogue is made higher than ca. 0.6 mM.

The present invention circumvents the necessity for insulin self-assembly as a mechanism to achieve a formulation of sufficient chemical stability and of sufficient physical stability to meet or exceed regulatory standards. Chemical degradation refers to changes in the arrangement of atoms in the insulin molecule, such as deamidation of Asn, formation of iso-Asp, and breakage of disulfide bridges. The susceptibility of n to al degradation is correlated with its thermodynamic stability (as probed by chemical denaturation experiments); because it is the monomer that is the species most tible to chemical degradation, its rate is d by sequestration of monomers within self-assemblies. al degradation refers to fibril formation llation), which is a non-native form of self-assembly that leads to linear structures containing thousands (or more) of insulin protomers in a beta-sheet rich conformation. lation is a serious concern in the manufacture, storage and use of insulin and insulin analogues above room temperature. Rates of fibrillation are enhanced with higher temperature, lower pH, agitation, or the presence of urea, guanidine, ethanol co-solvent, or hydrophobic surfaces. Current US drug tions demand that insulin be discarded if fibrillation occurs at a level of one percent or more. Because fibrillation is enhanced at higher temperatures, patients with DM optimally rrrust keep insulin refrigerated prior to use. Fibrillation of insulin or an insulin ue can be a particular concern for such patients utilizing an external n pump, in which small amounts of insulin or insulin analogue are injected into the patient’s body at regular intervals. In such a usage, the insulin or insulin analogue is not kept refrigerated within the pump apparatus, and fibrillation of n can result in blockage of the catheter used to inject n or insulin analogue into the body, potentially resulting in ictable fluctuations in blood glucose levels or even dangerous hyperglycemia. At least one recent report has indicated that insulin Lispro (KP—insulin, an analogue in which residues B28 and B29 are interchanged relative to their positions in wild-type human insulin; trade name Humalog®) may be ularly susceptible to fibrillation and resulting obstruction of insulin pump catheters. Insulin exhibits an se in degradation rate of 10-fold or more for each 10° C increment in temperature above ° C; accordingly, guidelines call for storage at temperatures < 30° C and preferably with refrigeration. Such formulations typically include a predominance of native insulin self- assemblies.

The present theory of protein fibrillation posits that the mechanism of fibrillation proceeds via a partially folded intermediate state, which in turn aggregates to form an amyloidogenic nucleus. In this theory, it is possible that amino—acid substitutions that stabilize the native state may or may not stabilize the lly folded intermediate state and may or may not increase (or decrease) the free-energy barrier n the native state and the intermediate state. Therefore, the current theory indicates that the tendency of a given amino—acid substitution in the insulin molecule to increase or decrease the risk of ation is highly ictable; in particular the lag time observed prior to onset of detectable ation does not ate with ements of the thermodynamic stability of the native-state monomer (as probed by chemical ration experiments). Whereas a given substitution may stabilize both the overall native state and amyloidogenic partial fold—and so delay the onset of fibrillation—another substitution may stabilize the native state but not the amyloidogenic partial fold and so have little or no effect on the lag time. Still other substitutions may destabilize the native state but stabilize the amyloidogenic partial fold, and so lead to accelerated fibrillation despite its apparent stabilizing properties.

There is a need, therefore for an insulin ue that displays rapid PK/PD for the treatment of DM under a broad range of insulin concentrations from 0.6 mM to 3.0 mM (typically corresponding to formulation strengths in a range from U-lOO to U—500) while ting at least a portion of the activity of the corresponding wild-type insulin, ining at least a portion of its chemical and/or al stability.

SUMMARY OF THE INVENTION It is an aspect of the present invention to provide insulin ues that provide zinc- free monomeric and dimeric species of ent chemical stability and physical stability to enable their formulation at a range of protein concentrations and in a form that confers rapid absorption following subcutaneous injection. The present invention addresses previous limitations for ultra-concentrated insulin formulations and insulin analogues formulations, namely, that they still do not act sufficiently quickly to optimize post-prandial glycemic control or enable use in insulin pumps. The claimed ion circumvents previous design restrictions, including those regarding substitution of PheB24, through the incorporation of a non-standard amino-acid substitution at position B24. The non-standard amino-acid side chain (2F-PheBz4; also designated ortho-monofluoro-Phe324) at position 324 markedly stabilizes the isolated insulin monomer. This is ed by substitution of an aromatic amino-acid side chain by a n—modified aromatic analogue, similar in size and shape to Phenylalanine, where the analogue then maintains at least a portion of biological activity of the corresponding insulin or insulin analogue ning the native aromatic side chain. Further, the modified side chain reduces the cross-binding of insulin to the Type-I IGF receptor R) and modulates binding to the n or such that the aberrant mitogenic properties conferred by the stabilizing substitution HisBlOfi Asp are circumvented. It is another aspect of the present invention that the 2-F-Phe}324 modification is combined with an acidic side chain at position B10 (Asp or Glu) such that the resulting analogue has an affinity for IGF-IR similar to that of wild-type human insulin.

It is r aspect of the present invention that such an n analogue may be formulated in at pH 7—8 at strengths from U—lOO to U—500 (approximately 0.6 — 3.0 mM), optionally in zinc-free formulations, with preservation of PK/PD ties similar to, or more rapid and less prolonged than, those of regular formulations of wild-type human insulin at strength U-lOO. In one particular embodiment, the concentration of insulin in the formulation is at least 2 mM. It is yet another aspect of the present invention that the insulin analogue ning 2F-Phe}324 and an acidic side chain at position B10 may contain additional substitutions in the A chain or B chain that further enhance chemical or physical stability or that further impair self-assembly.

In l, the present invention es a pharmaceutical formulation sing insulin having a t insulin B-chain polypeptide ning an ortho-monofluoro- Phenylalanine substitution at position B24 in relation to the sequence of human insulin, in combination with a substitution of an amino acid containing an acidic side chain at position B10 in relation to the sequence of human insulin selected from Aspartic Acid and Glutamic Acid, wherein the insulin is present at a tration of between 0.6 mM and 3.0 mM. In some particular ments the pharmaceutical formulation contains insulin at a concentration of at least 2 mM. In one particular embodiment, the pharmaceutical formulation contains insulin at a concentration of 2.4 mM or more.

In addition or in the alternative, the insulin analogue may be a mammalian insulin analogue, such as an analogue of human insulin. In one set of embodiments, the B-chain polypeptide comprises an amino-acid sequence selected from the group consisting of SEQ. ID.

NOS. 4-7 and ptides having three or fewer additional amino-acid substitutions thereof. In still another ment, the A chain contains a substitution at position A8 (SEQ. ID, NO. 8 in addition to B—chain cations) selected from the group consisting of SEQ. ID. NOS. 4-7.

In another embodiment, the insulin analogue may optionally contain a non-standard amino-acid substitution at position 29 of the B chain. In one example, the andard amino acid at B29 is norleucine (Nle). In another example, the non-standard amino acid at B29 is omithine (Orn). In still other examples, the non—standard amino acid may be Aminobutyric acid, ropionic acid, Diaminobutyric acid, or Diaminopropionic acid.

Also provided is a c acid encoding an insulin analogue comprising a B-chain polypeptide that incorporates a non-standard amino acid at position B24. In one example, the non—standard amino acid is encoded by a stop codon, such as the nucleic acid sequence TAG.

An expression vector may comprise such a nucleic acid and a host cell may contain such an expression vector.

The invention also provides a method of lowering the blood sugar level ofa patient.

The method comprises administering a physiologically effective amount of an insulin analogue or a physiologically acceptable salt thereof to the patient, wherein the insulin analogue or a physiologically acceptable salt thereof contains a n polypeptide incorporating an orthomonofluoro-Phenylalanine (2F-Phe) at position B24 and an Asp or Glu substitution at position B10. In still another ment, the insulin analogue is a mammalian insulin analogue, such as an ue of human insulin. In some embodiments, the B-chain polypeptide comprises an amino-acid sequence selected from the group consisting of SEQ. ID. NOS. 4-7 and polypeptides having three or fewer additional amino—acid substitutions thereof. In other embodiments, the A- chain polypeptide comprises an amino-acid sequence selected from the group consisting of SEQ.

ID. NOS. 8 in combination with a B-chain polypeptide comprising an acid sequence selected from the group consisting of SEQ. ID. NOS. 4-7.

It is a further aspect of the present invention to e a polypeptide comprising a variant insulin B-chain polypeptide sequence containing an ortho-monofluoro-Phenylalanine substitution at position B24 in on to the sequence of human insulin, in combination with a substitution of an amino acid containing an acidic side chain at position B10 in relation to the sequence of human insulin, and a substitution of a andard amino acid at position B29 in relation to the ce of human insulin selected from the group ting of Omithine, Diaminobutyric acid, Diaminopropionic acid, Norleucine, Aminobutyric acid, and Aminopropionic acid. In some embodiments, the polypeptide may be a proinsulin analogue or single—chain insulin ue.

BRIEF PTION OF THE SEVERAL VIEWS OF THE DRAWINGS FIG. I a schematic representation of the sequence of human insulin indicating the position of residue B24 in the B chain. is a ribbon model of an insulin monomer showing aromatic e of PheB24 in relation to the three disulfide bridges. The ing side chains of LeuBIS (arrow) and Phe1324 are shown. The A- and B chains are otherwise shown in light and dark gray, respectively, and the sulfur atoms of cysteines as circles. is a space—filling model of insulin showing the Phe side chain within a pocket at the edge of the hydrophobic core. is a series of ball and stick (top) and space-filling (bottom) representations of phenylalanine (Phe). is a series of ball and stick (top) and space-filling (bottom) representations of 2F-Phe. is a graph showing the results of or-binding studies of insulin analogues.

Relative activities for the B isoform of the insulin receptor (IR—B) are determined by competitive binding assay in which receptor-bound 125I-labeled human insulin is displaced by increasing concentrations of human insulin (0) or its analogues: DKP—insulin (A) and 2F—PheB24—DKP— insulin (V); results of curve fitting are summarized in Tables 2 and 3. is a histogram g extent of ligand—stimulated IGF-I or autophosphorylation. IGF-I receptor-deficient mouse embryo fibroblast cells stably expressing the human IGF-I receptor were serum-starved overnight and then treated with 10 nM ligand for 5 min and cell lysates prepared and analyzed for phosphorylated IGF-I receptor (IGF-IR) by ELISA. Autophosphorelation by 2F-DKP is similar with HI. shows the results of a breast-cancer—related MCF-7 colony formation assay for mitogenecity. MCF-7 human breast cancer cells were analyzed for colony formation in soft agar (reflecting tumorigenic ial) in the presence of 10 nM ligands after 1—week growth. enic potential of 2F-Phe -DKP was comparable to wild-type human n and untreated cells. provides a graph of CD-detected guanidine denaturation. Chemical denaturation of human insulin (HI, 0), insulin Lispro (KP, :1), AspBlO-KP-insulin (DKP, O) and 2F-PheB24-DKP—insulin (A) insulin analogs. a were collected at 25 0C in phosphate-buffer saline (pH 7.4). Unfolding was monitered by CD at 222 nm. The ity of the BZ4-DKP analogue exhibits a gain of 0.6(i0.2) and 1.6(i0.2) kcal/mol in stability (DDGU) relative to DKP- insulin and human insulin, respectively (see Table 4). is a histogram comparing the fibrillation lag times of insulin analogues.

Thioflavin T fluorescence monitered fibrillation lag time. Samples were gently agitated at 37 °C and pH 7.4 in Zn-free phosphate-buffered saline. 2F-DKP-insulin was 3.7 and ld more resistant to ation (as probed by lag times) relative to insulin Lispro and wild—type human insulin, respectively. provides a cal summary of the pharmacodynamics in anesthetized pigs of 2F-PheB24-DKP-insulin at U-400 strength (in zinc-free Lilly diluent containing 5 mM ethylenediaminetetraacetic acid (EDTA) at pH 7.4; middle bar) in relation to current n products g (U-100 strength; top bar) and Humulin R U-SOO m bar). provides a structural depiction of the l structure of 2F-Phe in the context of a zinc KP-insulin hexamer. (A) Ribbon model of wild-type human insulin as a T3ng zinc hexamer. (B) Corresponding ribbon model of 2F-Phe1324-KP-insulin in the same crystal form. The variant T3Rf3 structure is similar to that of the parent hexamer, trating lack of long-range structural perturbations and accommodation of the fluorine atom at a native-like dimer interface. illustrates the electron density surrounding 2F-Phe1324 in the crystal ure of 2F-Phe1324 as determined at a resolution of 2.5 A. (A) 2F-Phe1324 and oring electron 824 and neighboring electron density in the Rf-state density in the T-state protomer. (B) 2F-Phe protomer. The orientation of the B24 ring and interactions of the fluoro moiety differ n the two conformational states.

DETAILED DESCRIPTION OF THE INVENTION The present invention is directed an insulin analogue that enables rapid PK and PD to be maintained at a broad range of insulin concentrations from U-lOO to U-SOO. The analogue then ins at least a portion of biological activity of the corresponding unmodified insulin or insulin analogue and maintains similar or enhanced thermodynamic stability and resistance to fibril formation. We have invented an insulin analogue with PK/PD properties similar to or more rapid than regulation formulations of wild-type human insulin at U—lOO strength (e. g., Humulin R® U—100; Eli Lilly and Co.) such that these PK/PD properties are not significantly affected by the concentration ofinsulin analogue in the range 0.6 mM — 3.0 mM.

The present invention pertains to a non-standard fiuorous ation at position B24 to e the properties of concentrated n formulations with respect to rapidity of absorption following subcutaneous injection. In one instance the insulin analogue is an engineered dimer that contains acidic substitutions (Glu or Asp) at on B10, introduced to prevent binding of zinc ions by native residue HisBIO and to destabilize the trimer interface of insulin as defined in molecular structures of Zinc insulin rs. In another instance, the analogue is an engineered monomer that ns, in addition to the acidic tutions at position B10 described above, additional substitutions at positions B28 and/or B29, introduced to destabilize the classical dimer interface of insulin as defined in molecular structures of zinc insulin rs and zinc-free dimers. In yet another instance the dimeric and monomeric ues described above may contain an additional substitution at position A8.

In either of two particular embodiments (2F-PheBz4-DKP-insulin (where DKP represents AspBlo, Lys1328 and ProBZg), and 2F-PheBZ4-[AspB 10, OmB29]—insulin; where Om designates ornithine) the present invention provides an insulin analogue that exhibits an affinity for the Type I IGF or similar to or lower than that of wild-type human insulin, an activity in stimulating the autophosphorylation of the Type I IGF receptor that is r to or lower than that of wild-type human insulin, and an activity in stimulating the proliferation of a human breast-cancer—derived cell line that is similar to or lower than that of wild-type human insulin.

The present invention is not limited, r, to 2F-Phe1324—derivatives of human insulin and its analogues. It is also envisioned that these substitutions may also be made in dimeric and monomeric analogues derived from animal insulins such as porcine, bovine, , and canine insulins, by way of non—limiting examples.

It has been discovered that BZ4-DKP-insulin and 2F-PheB24-[AspBlo, Orn829]- insulin, when ated in Lilly Diluent and following subcutaneous injection in a male Lewis rat rendered diabetic by streptozotocin, will direct a reduction in blood glucose concentration with a potency similar to that of ype human n in the same formulation. It has also been discovered that 2F-PheBZ4-DKP-insulin and 2F-PheB24-[AspB10, -insulin, when formulated in Lilly Diluent and following subcutaneous injection in an anesthetized Yorkshire pig whose endogenous b-cell secretion of insulin was suppressed by enous administration of octreotide, will direct a ion in blood glucose concentration with a potency similar to that of wild-type human insulin in the same formulation.

In addition or in the alternative, the insulin analogue of the present invention may contain a standard or non-standard amino—acid substitution at position 29 of the B chain, which is lysine (Lys) in wild-type insulin. In one example, the non-standard amino acid at B29 is norleucine (Nle). In another example, the non—standard amino acid at B29 is ornithine (Om).

Furthermore, in view of the similarity between human and animal insulins, and use in the past of animal insulins in human patients with diabetes mellitus, it is also envisioned that other minor modifications in the sequence of insulin may be introduced, especially those substitutions considered “conservative.” For example, onal substitutions of amino acids may be made within groups of amino acids with similar side chains, without departing from the present invention. These include the neutral hydrophobic amino acids: Alanine (Ala or A), Valine (Val or V), Leucine (Leu or L), Isoleucine (Ile or I), Proline (Pro or P), Tryptophan (Trp or W), Phenylalanine (Phe or F) and Methionine (Met or M). Likewise, the neutral polar amino acids may be substituted for each other within their group of Glycine (Gly or G), Serine(Ser or S), Threonine (Thr or T), Tyrosine (Tyr or Y), Cysteine (Cys or C), ine (Glu or Q), and Asparagine (Asn or N). Basic amino acids are ered to include Lysine (Lys or K), Arginine (Arg or R) and Histidine (His or H). Acidic amino acids are Aspartic acid (Asp or D) and Glutamic acid (Glu or E). Unless noted otherwise or wherever obvious from the context, the amino acids noted herein should be considered to be o acids. Standard amino acids may also be substituted by non-standard amino acids belong to the same chemical class. By way of non-limiting example, the basic side chain Lys may be replaced by basic amino acids of shorter side-chain length hine, Diaminobutyric acid, or Diaminopropionic acid). Lys may also be replaced by the neutral aliphatic isostere Norleucine (Nle), which may in turn be substituted by analogues containing shorter aliphatic side chains (Aminobutyric acid or Aminopropionic acid).

In one example, the insulin analogue of the present invention contains four or fewer conservative substitutions other than the 2F-Phe and B10 substitutions of the present invention. In a pair of particular examples, the formulation containing a variant B-chain polypeptide ce also contains an Asn or Lys substitution at position B3 ve to human insulin. In addition or in the alternative, the formulation may additionally include an insulin A- chain ptide sequence containing a Glutamic acid substitution or a Histidine tution at position A8.

As used in this specification and the claims, various amino acids in insulin or an insulin analogue may be noted by the acid residue in question, followed by the position of the amino acid, ally in superscript. The position ofthe amino acid in question includes the A— or B chain of insulin where the substitution is located. Thus, Phe1324 denotes a phenylalanine at the twenty-fourth amino acid of the B chain of insulin. Fluoro-derivatives of aromatic rings retain planarity, but differ in bution of p electrons leading to changes in electrostatic potential as rated in front and side views of Phenylalanine (Fig. 3A) relative to 2F— Phenylalanine (Fig. 3B). As used herein, the d position of a particular substitution should be understood to be the position ve to wild type human insulin, regardless of the particular species being used in any particular embodiment under discussion. In this way, the location of a substitution will be identifiable regardless of any insertions, extensions or deletions in a particular ptide. 1324 modification - The present invention envisions that 2F at Phe introduces an electronegative atom and electrostatic dipole moment that result in (i) dynamic stabilization of the n monomer and (ii) an alteration in the functional character of the receptor-binding surface. Whereas there are substitutions known in the art that enhance the stability of insulin in concern with augmentation of receptor binding, 2F-Phe1324 stabilizes n while decreasing receptor binding. In particular, this alteration serves to counteract the effects of acidic substitutions at position B10 (Asp or Glu) to enhance binding to, and signaling through, the Type I IGF receptor; this alteration serves to counteract the effects of such B10 substitutions to e binding to the insulin or, presumably by reducing the residence time of the analogue on the receptor; and by means of these and other possible mechanisms, 2F-PheB24 enables the incorporation of acidic residues at B10 without incurring excess mitogenicity relative to wild-type human n.

The phenylalanine at B24 is an invariant amino acid in functional insulin and contains an aromatic side chain. The biological importance of Phe in insulin is indicated by a clinical mutation (Ser ) causing human diabetes mellitus. While not wishing to be bound by , Phe1324 is believed to pack at the edge of a hydrophobic core at the classical receptor binding surface. The models are based on a crystallographic protomer (2-Zn molecule 1; Protein Databank identifier 4INS). Lying within the C—terminal B-strand of the B chain ues B24- B28), Phe1324 s the central a—helix (residues B9-B19) (Fig. 2A). In the insulin r BIS and CysBl9; one face and edge of the aromatic ring sit within a shallow pocket defined by Leu the other face and edge are exposed to solvent (Fig. 2B). This pocket is in part surrounded by main-chain carbonyl and amide groups and so creates a complex and asymmetric electrostatic environment with irregular and loose steric borders. In the insulin dimer, and within each of the side chain of Phe packs Within. - three dimer interfaces of the insulin r, the a more tightly contained spatial environment as part of a cluster of eight aromatic rings per dimer interface (TyrBlG, PheB24, l’he1325 , Tyr1326 and their dimer-related mates). Irrespective of theory, substitution of the aromatic ring of PheB24 by a 2F derivative preserves l hydrophobic packing within the dimer interface while ucing favorable asymmetric electrostatic interactions within the insulin monomer.

The present invention pertains to a andard modification at position B24 to improve the properties of ultra—concentrated formulations of dimeric or monomeric insulin analogues with respect to physical stability, chemical stability, and mitogenicity. Because of these improvements, the n analogues can be formulated at strengths greater than U-100 and up to U-500 such that, irrespective of the concentration of insulin analogue, the formulation maintains a rapidity of absorption and pharmacologic activity following subcutaneous ion similar to that ofa regular wild-type human insulin U-100 formulation; examples ofthe latter are Humulin® R U-100 (Eli Lilly and Co) or n® R U-100 (Novo-Nordisk). In one instance the n analogue contains 1324 in association with an acidic substitution (Asp or Glu) at position B10. In yet other instances the non-standard amino-acid tution at B24 is accompanied both by an acidic substitution at B10 and by a non-standard substitution at position B29 or by three or fewer standard substitutions elsewhere in the A- or B chains.

It is envisioned that the substitutions of the present invention may be made in any of a number of existing insulin analogues. For example, the ortho-fluoro tive of Phenylalanine at position B24 (2F-PheB24) provided herein may be made in insulin analogues that contain an acidic residue at on B10 in the context of insulin Lispro ([LysB28, PrOB29]-insulin, herein abbreviated KP-insulin), insulin Aspart (Asszg-insulin), insulin Glulisine ([LysB3, GluB29]- insulin), or other modified insulins or insulin analogues, or within various pharmaceutical ations, such as regular insulin, NPH insulin, lente insulin or ultralente insulin, in addition to human insulin. Insulin Aspart contains an Asp substitution and is sold as Novalog® whereas insulin Lispro contains Lys1328 and Pro substitutions and is known as and sold under the name B28 and ProB 9and2 .

Humalog®; insulin Glulisine ns substitutions Lys 1s known as and sold under the name Apidra®. These analogues are described in US Pat. Nos. 5,149,777, 5,474,978, and 7,452,860. These analogues are each known as fast-acting insulins.

The amino-acid sequence of human ulin is provided, for ative purposes, as SEQ ID NO: 1.

SEQ ID N041 (human proinsulin) Phe-Val-Asn-Gln-His-Leu-Cys-Gly-Ser—His-Leu-Val-Glu-Ala-Leu-Tyr—Leu-Val-Cys— Gly-Glu-Arg-Gly-Phe-Phe-Tyr-Thr—Pro-Lys-Thr-Arg—Arg—Glu-Ala-Glu-Asp-Leu-Gln-Val-Gly— Gln-Val-Glu-Leu-Gly—Gly—Gly-Pro—Gly—Ala—Gly-Ser-Leu-Gln-Pro-Leu-Ala-Leu-Glu-Gly—Ser- Leu-Gln-Lys-Arg-Gly-Ile-Val-Glu—Gln-Cys-Cys-Thr-Ser—Ile-Cys-Ser-Leu-Tyr—Gln-Leu-Glu- Asn-Tyr—Cys-Asn The amino-acid sequence of the A chain of human insulin is provided as SEQ ID NO: SEQ ID NO: 2 (human A chain) Gly—Ile-Val-Glu—Gln—Cys—Cys-Thr—Ser—Ile-Cys—Ser—Leu—Tyr-Gln—Leu-Glu-Asn—Tyr—Cys— The amino-acid sequence of the B chain of human insulin is provided as SEQ ID NO: SEQ ID NO: 3 (human B chain) l—Asn—Gln-His-Leu-Cys-Gly—Ser—His—Leu-Val—Glu-Ala—Leu-Tyr—Leu-Val-Cys- Gly-Glu-Arg-Gly—Phe-Phe-Tyr—Thr—Pro-Lys-Thr The amino—acid sequence of a B chain of human insulin may be modified with a substitution of a ortho-monofluoro-Phenylalanine (2F-Phe) at position B24. An e of such a ce is provided as SEQ. ID. NO 4.

SEQ ID NO: 4 Phe-Val- Xaas-Gln-His-Leu-Cys-Gly-Ser-Xaa4-Leu-Val-Glu-Ala—Leu-Tyr—Leu-Val-Cys- Gly-Glu-Arg-Gly— he-Try-Thr-Xaa2-Xaa3-Thr [Xaal is 2F-Phe; Xaaz is Asp, Pro, Lys, or Arg; X2133 is Lys, Pro, or Ala; Xaa4 is Asp or Glu; and Xaas is Asn or Lys] ' Substitution of a 2F-Phe at position B24 may optionally be combined with non- standard substitutions at position B29 as provided in SEQ. ID. NO 5.

SEQ ID NO: 5 Phe-Val-Asn-Gln-His-Leu-Cys-Gly—Ser—Xaa4-Leu-Val—Glu—Ala—Leu—Tyr—Leu-Val-Cys— Gly-Glu—Arg—Gly— XaaI-Phe-Try-Thr- Xaaz-Xaag—Thr [Xaa] is 2F-Phe; Xaaz is Asp, Glu, or Pro; Xaa3 is Ornithine, Diaminobutyric acid, Diaminoproprionic acid, Norleucine, Aminobutric acid, or Aminoproprionic acid; and Xaa4 is Asp or Glu] r combinations of other substitutions are also within the scope of the present ion. It is also envisioned that the substitutions and/or additions of the present invention may also be combined with substitutions of prior known n ues. For example, the amino-acid sequence of an analogue of the B chain of human insulin containing the Lys and Pro substitutions of insulin Lispro, in which the 2F-Phe1324 substitution may also be introduced, is provided as SEQ ID NO: 6.

SE ID NO: 6 Phe—Val-Asn-Gln—His—Leu-Cys—Gly-Ser— Xaaz-Leu—Val-Glu-Ala-Leu-Tyr-Leu-Val-Cys- Gly—Glu—Arg-Gly-Xaa] -Phe—Tyr—Thr—Lys-Pro-Thr [Xaa] is 2F-Phe, and Xaaz is Asp or Glu] Similarly, the amino—acid sequence of an analogue of the B chain of human insulin containing the Asp1328 substitution of insulin Aspart, in which the 2F—Phe1324 tution may also be introduced, is provided as SEQ ID NO: 7.

SEQ ID NO: 7 Phe—Val—Asn-Gln-His-Leu—Cys—Gly-Ser—Xaag-Leu-Val—Glu—Ala—Leu-Tyr-Leu- Val-Cys-Gly-Glu-Arg-Gly-Xaa]-Phe-Tyr-Thr-fip—Lys-Thr.

[Xaal is 2F-Phe, and Xaaz is Asp or Glu] In still another embodiment, the B—chain insulin analogue polypeptide contains a Lysine at position B3, Glutamic acid at position B29, and ortho-monofluoro—Phenylalanine at position B24 as provided as SEQ ID NO: 8.

S_EQ_1D NO: 8 Phe-Val—Lfi-Gln-His-Leu—Cys-Gly—Ser- Xaag-Leu-Val—Glu—Ala—Leu—Tyr—Leu— Val—Cys-Gly—Glu-Arg-Gly-Xaal-Phe-Tyr—Thr—Pro—§]u—Thr.

[Xaal is 2F-Phe, and Xaaz is Asp or Glu] A 1324 substitution may also be introduced in combination with other insulin analogue tutions such as analogues of human insulin ning a substitution at residue A8 as described more fully in co—pending International Application No. PCT/USO7/00320 and US. Application Ser. No. 12/160,187. For example, the 2F-Phe1324 substitution may be present with HisA8 or GluA8 in which the variant A chain is provided in SEQ ID NO: 9, SEQ ID NO: 9 Gly—Ile-Val- Glu-Gln-Cys—Cys-Xaa1-Ser-Ile-Cys—Ser-Leu-Tyr-Gln-Leu-Glu-Asn- Tyr-Cys-Asn; wherein Xaa] is His or Glu.

The insulin analogues provided in SEQ ID NO: 4-8 may be prepared by trypsin— catalyzed semi—synthesis in which a des—octapeptide[B23-B30] fragment of AspBlO-insulin, GluBlO—insulin, or variants thereof containing an additional substitution at position A8, is employed as ed in SEQ ID NOS: 10 and 11 wherein the A and B chain are connected by cystines A7-B7 and 9 and wherein the A chain contains cystine A6—A1 1.

SEQ ID NO: ID (A chain) Gly-Ile-Val-Glu—Gln-Cys-Cys-Xaa-Ser—Ile-Cys-Ser—Leu-Tyr-Gln-Leu-Glu-Asn-Tyr—Cys- wherein Xaa is Thr, His, or Glu SEQ ID NO: 11 (B chain) Phe-Val-Asn-Gln-His-Leu-Cys-Gly—Ser—Xaa-Leu-Val—Glu-Ala—Leu-Tyr—Leu-Val-Cys- Gly—Glu—Arg wherein Xaa is His or Glu. n-mediated semisynthesis also s a synthetic octapeptide containing ortho-monofluoro-Phenylalanine (2F—Phe) as provided in SEQ ID NOS: 12-14.

SEQ ID NO: 12 Gly-Xaal-Phe-Tyr—Thr—Pro-Xaaz—Thr.

[Xaa] is 2F-Phe and X2182 is Lys containing a removable ting group attached to its eamino function] SEQ ID NO: 13 Gly-Xaal -Phe-Tyr-Thr—Pro-Xaag-Thr.

[Xaal is 2F-Phe and Xaaz is Glu] SEQ ID NO: 14 Gly-Xaal-Phe—Tyr—Thr-Pro-Xaa2-Thr.

[Xaa] is 2F-Phe and Xaaz is Norleucine, Ornithine, Diaminobutyric Acid, or Diaminopropionic Acid] SE ID NO: 15 Gly-Xaa,-Phe-Tyr-Thr-Xaa2-Pro—Thr.

[Xaa] is 2F-Phe and X21212 is Asp or Glu] SEQ ID NO: 16 Gly-Xaa]-Phe-Tyr—Thr-flp-Xaag-Thr.

[Xaa] is 2F-Phe and Xaaz is Lys containing a removable protecting group attached to its e-amino function] SEQ ID NO: 17 Gly-Xaa1-Phe-Tyr-Thr-L)§-Prg-Thr.

[Xaal is 2F-Phe] An monofluoro-Phenylalanine substitution at B24 may also be introduced as an additional tution into a single-chain n analogue as disclosed for example in US.

Patent No. 957.

Ortho-monofluoro-Phenylalanine (2F-Phe) was introduced within an engineered insulin monomer of native activity, designated DKP-insulin, which contains the substitutions Asp1310 (D), Lys1328 (K), and Pro1329 (P). These three substitutions on the surface of the B chain are believed to impede formation of dimers and hexamers and to be incompatible with hexamer assembly in the absence or presence of zinc ions and in the e or presence of a phenolic preservative. ulin (which lacks the Asp substitution of DKP insulin) is the active ingredient of g® (also designated insulin Lispro), currently in clinical use as a rapid— acting insulin analogue formulation. The sequence of the B-chain polypeptide for this variant of DKP-insulin is provided as SEQ ID NO: 6. Ortho-monofluore-Phenylalanine (2F-Phe) was also introduced at position B24 within an engineered insulin monomer of ed activity, designated DDP-insulin, which contains the substitution AspBIO (D) in addition to the DP substitutions Asp1328 (K) and ProB29 (P) in accordance with the general scheme provided in SEQ.

ID. NO 4. 2F-Phe1324 was also introduced into non-standard human insulin analogues ning Omithine position B29 in accordance with the general scheme provided in SEQ. ID. NO 5.

The above ues of AspBIO-insulin were prepared by trypsin-catalyzed semi- synthesis and purified by high-performance liquid chromatography (Mirmira, R.G., and Tager, HS, 1989. J Biol. Chem. 264: 6349-6354.) This protocol employs (i) a synthetic octapeptide representing residues (N)—GF*FYTQT (including d residue (F*) and “KP” substitutions (underlined); SEQ ID NO: 15) and (ii) truncated analogue des-octapeptide[B23-B30]—insulin or, in the case of sulin analogues, AspBI0-des—octapeptide[B23—B30]-insulin (SEQ ID NO: 11). Because the octapeptide differs from the wild-type B23-B30 sequence (GF*FYTPKT; SEQ ID NO: 12) by interchange of Pro1328 and Lys1329 (italics), protection of the lysine e-amino group is not required during n treatment. In brief, des-octapeptide (15 mg) and octapeptide (15 mg) were dissolved in a mixture of dimethylacetamide/ 1,4-butandiol/0.2 M Tris acetate (pH 8) containing 10 mM calcium acetate and 1 mM ethylene diamine tetra-acetic acid (EDTA) (35:35:30, v/v, 0.4 mL). The final pH was adjusted to 7.0 with 10 mL of N—methylmorpholine.

The solution was cooled to 12 °C, and 1.5 mg of TPCK-trypsin was added and incubated for 2 days at 12 °C. An additional 1.5 mg of trypsin was added after 24 hr. The reaction was acidified with 0.1% trifluoroacetic acid and d by preparative reverse-phase HPLC (C4). Mass spectrometry using matrix-assisted laser desorption/ionization time—of—flight (MALDI—TOF; d tems, Foster City, CA) in each case gave expected values (not shown). The general protocol for solid—phase synthesis is as described (Merrifield et al., 1982. Biochemistry 21: 031). 9-fluoren—9-yl-methoxy—carbonyl (F-moc)—protected phenylalanine analogues were sed from Chem-Impex International (Wood Dale, IL).

The above protocol was also employed to prepare an analogue of AspBIO—human insulin in which Phe was substituted by 2-F-Phe and in which 8 was substituted by Asp (D) and Lys1329 was substituted by Pro (P). This analogue is designated 2F-PheB24-DDP-insulin wherein the acronym DDP refers in turn to the identity of the amino—acid residue at respective positions B10, B28, and B29.

The above protocol was also employed to prepare an analogue of AspBIO—human n containing Omithine (O) at position B29 and to introduce 2F-Phe1324 in this context. The method of preparation of this analogue exploited the andard amino-acid substitution at position 29 to eliminate the c site ordinarily t within the C-terminal octapeptide of the B chain (i.e., between Lys1329 and ThrB30) while maintaining a Proline (P) at position 28.

ProB28 is believed to contribute to the stability of the dimer interface within the insulin hexamer, and so this method of preparation provides near-isosteric models of wild-type insulin in which other ations may conveniently be incorporated without the need for cumbersome side— chain protection. This analogue is designated 2F-Phe1324—DPO-insulin wherein the m DPO refers, as above, to the identity of the amino-acid residue at respective ons B10, B28, and B29. The B24—modified insulin analogues were ted to some or all of the following assays. Biological potency was assessed in a diabetic rat model and by euglycemic clamp in anesthetized Yorkshire pigs; receptor-binding activity values shown are based on ratio of hormone-receptor dissociation constants relative to human n (the activity of human insulin is thus 1.0 by definition with standard errors in the activity values otherwise less in general than %); assays of hormone-stimulated autophosphorylation of the Type I IGF receptor were performed in a mouse embryo fibroblast expressing the human IGF-IR y provided by Drs.

Deepali Sachdev and Douglas Yee of the University of Minnesota); assays of mitogenicity in a human cell line employed breast-cancer-derived cell line MCF-7 as described (Milazzo G, Sciacca L, Papa V, Goldfine ID, i R. (1997) AspBlO-insulin induction of increased mitogenic responses and phenotypic changes in human breast epithelial cells: evidence for ed interactions with the insulin-like growth factor-I receptor. M01. og. 18, 19-25); thermodynamic stability values (free energies of unfolding; DGU) were assessed at 25° C based on a two—state model as extrapolated to zero denaturant concentration; resistance to fibril ion was evaluated by measurement of lag times (in days) required for initiation of protein fibrillation on gentle agitation at 300 C in zinc-free phosphate—buffered saline (pH 7.4) as described (Yang, Y., Petkova, A.T., Huang, K., Xu, B., Hua, Q.X., Y, I.J., Chu, Y.C., Hu, S.Q., Phillips, N.B., Whittaker, J., lsmail-Beigi, F., , R.B., Katsoyannis, P.G., Tycko, R., & Weiss, MA. (2010) An Achilles” Heel in an amyloidogenic protein and its repair. Insulin fibrillation and therapeutic design. J. Biol. Chem. 285, 10806—10821). Results of curve fitting are ized in Table 4 and rated in Figure 8.

Circular ism (CD) spectra were obtained at 4° C and/or 25° C using an Aviv spectropolarimeter (Weiss et al., Biochemistry 39: 15429—15440). Samples contained ca. 25 mM DKP-insulin or analogues in 50 mM potassium phosphate (pH 7.4); samples were diluted to 5 mM for guanidine-induced denaturation studies at 25° C. To extract free energies of unfolding, denaturation tions were fitted by non-linear least squares to a two-state model as described by Sosnick et al., Methods Enzymol. 317: 393-409. In brief, CD data q(x), where x indicates the concentration of denaturant, were fitted by a nonlinear least-squares program according to (7 007,20 »m.i-)/Ii'r + q”e q<x) = 3‘4 . 1 + e7(D(1”10—m.\‘)/RI where x is the concentration of ine and where (9/; and 63 are baseline values in the native and unfolded states. Baselines were imated by pre— and post—transition lines gA(x) =q/ilzo +mAx and gB(x) : quo +me_ The m values ed in fitting the variant unfolding transitions are lower than the m value obtained in fitting the wild—type unfolding curve.

To test whether this difference and apparent change in AGu result from an inability to measure the CD signal from the fully unfolded state, simulations were performed in which the data were extrapolated to plateau CD values at higher concentrations of guanidine; essentially identical estimates of AGu and m were obtained. Representative data are shown in Figure 7. The far- ultraviolet circular dichroism (CD) spectrum of the 2F-Phe -DKP-insulin ue is similar to those of the parent analogue DKP—insulin.

The baseline thermodynamic stability of ulin, as inferred from a ate model of denaturation at 25 °C, is 3.0 i 0.1 kcal/mole. CD—detected guanidine ration studies indicate that the 2F-Phe substitution is associated with a gain in thermodynamic stability in the context of KP-insulin (DDGu 1.1 :l: 0.2 kcal/mole) and in the context of DKP- insulin (DDGu 0.60 i 0.2 kcal/mole). r, the physical stability ofthe B24-DKP-insulin was found to be markedly greater than that of KP-insulin as evaluated in triplicate during incubation; the ns were made 300 uM in phosphate—buffered saline (PBS) at pH 7.4 at 30° C under gentle ion. The samples were observed for 20 days or until signs of precipitation or frosting ofthe glass vial were observed. Results are shown in Figure 8 (see also Table 4).

Relative receptor—binding activity is defined as the ratio of the hormone-receptor iation constants of analogue to wild-type human insulin, as measured by a competitive dlsplacement_ . I-human insulin., , Microtiter. . . plates (Nunc Max1sorb) were. assay us1ng strip incubated overnight at 4° C with AU5 IgG (100 ul/well of 40 mg/ml in phosphate-buffered saline). Binding data were analyzed by a two—site sequential model. Data were corrected for nonspecific binding (amount of radioactivity remaining membrane associated in the presence of 1 mM human insulin. In all assays the percentage of tracer bound in the absence of ing ligand was less than 15% to avoid ligand-depletion artifacts. Representative data are provided in Figure 4.

To assess hypoglycemic potencies of DKP—insulin analogues, DDP-insulin analogues, and DPO insulin analogues or there 2F-Phe1324 derivatives relative to ulin or wild—type human insulin in vivo, male Lewis rats (mean body mass ~300 grams) were rendered diabetic by treatment with streptozotocin. (This model proVides a probe of potency but not degree of acceleration of pharmacokinetics as (i) wild-type insulin, ulin, and 8-insulin exhibit similar patterns of effects of blood glucose concentration and (ii) these patterns are unaffected by the ce of absence of zinc ions in the formulation at a stoichiometry sufficient to ensure assembly of insulin hexamers.) Protein ons containing wild-type human insulin, insulin analogues, or buffer alone (protein—free e diluent obtained from Eli Lilly and Co.; composed of 16 mg glycerin, 1.6 mg meta-cresol, 0.65 mg phenol, and 3.8 mg sodium ate at pH 7.4.) were injected subcutaneously, and resulting changes in blood glucose were monitored by serial measurements using a al glucometer (Hypoguard Advance Micro—Draw . To ensure uniformity of formulation, insulin analogues were each re—purified by reverse-phase high— performance liquid chromatography (rp-HPLC), dried to powder, dissolved in diluent at the same maximum protein concentration (300 mg/mL) and re-quantitative by analytical C4 rp—HPLC; dilutions were made using the above buffer. Rats were injected aneously at time t = 0 with mg insulin in 100 u] of buffer per 300 g rat. This dose corresponds to ca. 67 mg/kg body weight, which corresponds in international units (IU) to 2 lU/kg body weight. esponse studies of KP-insulin indicated that at this dose a near-maximal rate of glucose disposal during the first hour following injection was achieved. Five rats were studied in the group receiving 2F— PheB24-DKP-insulin, 2F-PheB24-DDP—insulin, or 2F-PheBZ4-DPO, and five ent rats were studied in the l group receiving KP-insulin or wild-type human insulin; these rats were randomly selected from a colony of 30 diabetic rats. The two groups exhibited similar mean blood glucose concentrations at the start of the experiment. Blood was obtained from clipped tip of the tail at time 0 and every 10 minutes up to 90 min; in some studies the time period was ed to 180 min or 240 min. The efficacy of insulin action to reduce blood glucose concentration was calculated using the change in concentration over time (using mean squares and initial region of linear fall) divided by the concentration of insulin injected. These data thus suggest that the biological potency of 2F-Phe1324-DKP-insulin is equivalent to that of KP—insulin in a zinc hexamer formulation; the other 2F-Phe1324 insulin analogues were not tested in the rat model.

To assess PK, PD, and potency of insulin analogues in an animal model predictive of BIO . . . . pharmacologic properties in humans, 2F—Phe1324 derivatives of Asp -conta1n1ng human insulin analogues were investigated in adolescent Yorkshire farm pigs (weight 35-45 kg). On the day of study, each animal ent anesthesia induction with Telazol and general anesthesia with isoflurane. Each animal was endotreacheally intubated with continuous ring of oxygen saturation and dal expired C02. Although the animals were not diabetic, islet function was suppressed in the OR by subcutaneous ion of octreotide acetate (44 mg/kg) approximately min before beginning the clamp study and every 2 h thereafter. After IV catheters were placed and baseline euglycemia established with 10% dextrose infusion, an subcutaneous injection of the insulin was given through the catheter. In order to quantify peripheral insulin- mediated glucose uptake, a variable-rate e infusion was given to maintain a blood glucose concentration of approximately 85 mg/dl. This glucose infusion typically will be required for 5- 6 hours, i.e., until in control studies of Humulin® glucose infusion rates were typically observed to return to pre-insulin baseline values. Glucose trations were measured with a Hemocue 201 portable glucose analyzer every 10 min (with standard error 1.9%).

The computerized protocol for glucose clamping was as described (Matthews, D. R., and Hosker, J. P. (1989) Diabetes Care 12, 156-159). In brief, 2—ml blood samples for insulin assay were obtained ing to the following schedule: from 0 — 40 min after insulin delivery: -minute intervals; from 50 — 140 min: 10-minute intervals, and from 160 min — to the point when GIR is back to baseline: 20—min intervals. For PK/PD a 20-min moving mean curve fit and filter is applied. PD was measured as time to half—maximal effect (early), time to half- maximal effect (late), time to maximal effect, and area-under—the—curve (AUC) over baseline.

For each of these es, the fitted curve, not the raw data, were employed in subsequent analyses. Each of three pigs underwent two studies: one with Chlorolog and one at the same dosage (0.5 max dose) with U—500 ator n® R U—500 (Eli Lilly and Co., Indianapolis, IN) and U-lOO comparators Humalog® and l Humulin® (Lilly Laboratories, Indianapolis, IN). The s indicate that 2F-PheB24-DKP-insulin and 2F—PheB24—DDP-insulin retain rapid-acting PD when concentrated to U-400 strength (2.4 mM; 2F-PheB24-DKP-insulin) or U-500 strength (3.0 mM; 2F-PheB24-DDP-insulin). PD parameters are summarized in Table 1 and in graphical form in Figure 9.

Table 1.

PD Studies of 2F-Phe1324 Analogues in Anesthetized Yorkshire Pigsa Protein Strength Additive 11/2 2me } Tfix 11/2 [TM (late) A. Control Studies 0fHumulin® R U—500 (pigs 1-4)b wild-type U-500 none 122 min 240 min 357 min wild—type U-500 none 77 min 180 min 342 min wild-type U—500 none 100 min 180 min 342 min wild-type U-500 none 95 min 200 min 217 min B. Studies 0f2F-PheB24-DKP—insulin (pig 5)6 KP-insulin U-100 noned 61 min 120 min 193 min 2F-DKP-ins U—100 none 62 min 130 min 186 min KP-insulin U-400 EDTAe 105 min 190 min 274 min 2F-DKP—ins U-400 EDTAf 28 min 140 min 228 min C. Studies 0f2F-PheB24-DDP-insulin (pig 6% KP-insulin U-100 noned 36 min 100 min 160 min 2F-DDP-ins U-100 EDTAh 33 min 100 min 172 min D. Studies of2F—PheB24-DDP—insulin (pig 7)g wild—type U-500b none 95 min 200 min 271 min 2F—DDP-ins U-500 EGTAl 76 min 180 min 280 min aPD, pharmacodynamics. Key results are shown in bold. bFour different pigs were used in control studies of Lilly U-500 as formulated by the manufacturer (part A). 'l'hese animals differed in turn from used in the studies of 2F-l’heH24 analogs: the various pigs were eless r in age and body mass. CThe three trials of 2F-l’heBz4—DKP-insulin (abbreviated 2F-DKP-ins) were ted in a single pig. llKP-insulin was used as formulated by the manufacturer (Humalog®; Eli Lilly and C0.). eEDTA was added to a concentration of 5 mM to the formulation buffer used in the Lilly U-100 Humalog® product. 2‘This ue is abbreviated as 2F—DDP-ins. hEDTA was added to a concentration of 5 mM to a zinc-free formulation in which phosphate buffer was replaced by THAM buffer (2—aminohydroxymethyl-propane-1,3-diol); the formulation was otherwise similar to Lilly Diluent.

Because the AspBlO tution in the context of unmodified human insulin (AspBlo- n) was observed to exhibit enhanced mitogenicity ve to wild—type insulin in associated with excess mammary tumor formation in Sprague-Dawley rats (Oleksiewicz, M.B., Bonnesen, C., Hegelund, A.C., Lundby, A., Holm, G.M., Jensen, M.B., & Krabbe, J.S. (2011) Comparison of intracellular signalling by insulin and the hypermitogenic AspB10 analogue in MCF-7 breast adenocarcinoma cells. 1 Appl. Toxicol. 31, 329-41 and references therein), we undertook mammalian cell-based s of hormone—stimulated autophosphorylation of the Type I IGF receptor (IGF-IR) in a mouse embryo fibroblast cell lacking endogenous IGF receptors and stably transfected to s human IGF-IR; results are illustrated in Figure 5. The cells were grown to 75% confluence, starved of serum ght and then treated with 10 nM hormone (wild-type insulin, IGF—I, AspBlO-insulin, AspBIO-OmBzg-insulin, DKP—insulin, 2F—PheBz4-DKP- insulin, or 2F-Phe1324—DPO-insulin). Cell lysates were in each case prepared and analyzed for phosphorylated IGF-I receptor by anti-phospho—IGF-IR ELISA as described by the vendor (Cell Signaling Technologies, Inc.). Studies were performed in triplicate. The s demonstrate that whereas AspBlO-insulin exhibits more profound autophosphorylation ve to human insulin, the 1324 modification restores the level of autophosphorylation to that indistinguishable from that of ype human insulin. Further, the set of hormones and analogues was tested for their ability to stimulate the proliferation of human breast-cancer cell line MCF-7 as described (Milazzo G, Sciacca L, Papa V, Goldfine ID, Vigneri R. (1997) AspBlO- insulin induction of increased mitogenic responses and phenotypic changes in human breast epithelial cells: ce for enhanced ctions with the insulin—like growth factor-I receptor.

M01. Carcinog. 18, 19-25). The cancer cells were analyzed for colony formation in soft agar (reflecting tumorigenic potential) in the presence of 10 nM ligands after 1 week of ; results are illustrated in Figure 6. Whereas AspBlO-insulin stimulates more growth than does wild—type human insulin, the r addition of the 2F-Phe1324 modification reduces mitogenicity to a level inguishable from that of wild-type human insulin.

Structural accommodation ofthe 2F—Phe modification was analyzed in a monomeric context h 2D-NMR s of 2F-PheBz4—DKP-insulin. A native-like pattern of lH-NMR chemical shifts and nuclear Overhauser effects (NOES) was observed; molecular models based on distance-geometry and simulated annealing were similar to those obtained in 2D-NMR s of DKP-insulin. Additional structural studies were undertaken by single- crystal X-ray crystallography. Crystals based on zinc KP-insulin hexamers were grown as described (Liu, M., Wan, Z., Chu, Y.C., Aladdin, H., Klaproth, B., Choguette, M., Hua, Q.X., Mackin, R., Rao, J.S., De Meyts, P., Katsoyannis, P.G., Arvan, P. & Weiss, M.A. (2009) The crystal ure of a “nonfoldable” insulin: impaired folding efficiency despite native ty. J.

Biol. Chem. 284, 35259-35272). In brief, crystals were grown by hanging-drop vapor diffusion in the presence of a 1:25 ratio of Zn2+ to protein monomer and a 3.721 ratio of phenol to protein monomer in Cl . Drops consisted of 1 ul of protein solution (10 mg/ml in 0.02 M HCl) mixed with 1 ul of oir on (0.02 M Tris—HCl, 0.05 M sodium citrate, 5% acetone, 0.03% phenol, and 0.01% zinc acetate at pH 8.1). Each drop was ded over 1 ml of reservoir solution. Crystals (space group R3) were obtained at room temperature after two weeks. Data were collected from single crystals mounted in a rayon loop and flash frozen to 100 K. Reflections from 24.98-2.50 A were measured on CCD detector system on synchrotron radiation at Advanced Photon Source (APS) at Argonne National Laboratory, Chicago. Data were sed with programs HKL2000 (Z. Otwinowski and W. Minor (1997) Processing of X- ray Diffraction Data Collected in Oscillation Mode ", Methods in Enzymology, Volume 276: Macromolecular Crystallography [C.W. Carter, Jr. & R. M. Sweet, Eds], Academic Press (New York), part A, pp. 307-26.). The l exhibited unit-cell parameters: a=b=77.98 A, c=37.14 A, a=B=90°, y=120°. The structure was determined by molecular replacement using CNS.

Accordingly, a model was obtained using the native TR dimer (Protein Databank (PDB) identifier lLPH following removal of all water molecules, zinc and chloride ions). A translation- function search was performed using coordinates from the best solution for the rotation function following analysis of data between 15.0 and 4.0 A resolutions. Rigid—body refinement using CNS, employing overall anisotropic temperature factors and bulk-solvent tion, yielded values of 0.29 and 0.33 for R and Rfi-ee, respectively, for data between 25.0 and 3.0A resolution.

Between refinement cycles, 2F,,—FC and FO-FL. maps were calculated using data to 2.50 A tion; zinc and de ions and phenol les were built into the structure using the program 0. The geometry was continually monitored with PROCHECK; zinc ions and water molecules were built into the ence map as the refinement proceeded. Calculation of omit chain N terminus of each monomer) and further maps ially in the first eight residues of B refinement were carried out using CNS, which implement maximum-likelihood n-angle dynamics and conjugate-gradient refinement.

The structures are similar to those of the parent analog as illustrated in Figure 10. s the location of the aromatic ring is similar to that of the unmodified residue in wild—type n, the T and Rf—state protomers exhibit distinct mations as illustrated by the electron- density maps shown in Figure 11. In each case the orientation of the 2F-Phe aromatic ring with respect to an individual insulin protomer leaves a native-like outer dimerization interface.

Irrespective of theory, a T-like orientation was also observed in 2D-NMR s of the monomeric 2F-PheB24-DKP-insu1in analogue and is likely to accrue ble electrostatic interactions, thereby rationalizing the increased thermodynamic stabilities of 2F-Phe insulin analogues. In this conformation the electronegative fluoro-substituent is near the partial ve 325 B26 s of two amide nitrogens (the main-chain peptide NH moieties of Phe and Tyr ).

To test the compatibility of the 2F-Phe modification with dimerization (as pertinent to 2F-PheB24-DPO-insulin and related analogues in which residues B28 and B29 do not B24 modification impair dimerization), the 2F-Phe was introduced into framework otherwise capable of hexamer formation to enable spectroscopic analysis of cobalt-mediated (COB) hexamer assembly and the kinetic analysis of hexamer disassembly. The kinetic ity of insulin analogue hexamers was assessed at 25° C relative to that of the wild—type human insulin hexamer as a Co2+ complex in the presence of 2.2 cobalt ions per hexamer and 50 mM phenol in a buffer consisting of 10 Tris-HCl (pH 7.4). The assay, a modification of the procedure of Beals et al. aum, D.T., Kilcomons, M.A., DeFelippis, M.R., & Beals, J.M. Assembly and B28 B29 - - - dissociation of human insulin and Lys Pro -1nsu11n hexamers: a comparison study. Pharm Res. 14, 25-36 (1997)), employs l absorbance at 500-700 nm to monitor the R6-hexamer- c d—d transitions characteristic of tetrahedral cobalt ion coordination. Although the solution at equilibrium contains a predominance of cobalt insulin hexamers or cobalt insulin analogue hexamers, this equilibrium is characterized by opposing rates of insulin ly and disassembly. To initiate the assay, the solution is made 2 mM in ethylene-diamine—tetra—acetic acid (EDTA) to sequester free cobalt ions. The time course of decay of the R6—specific absorption band on addition of EDTA provides an estimate of the rate of hexamer disassembly. s wild-type insulin exhibited a time constant of 419 d: 51 seconds, KP-insulin exhibited a time constant of 114 i 13 seconds in accordance with its accelerated pharmacokinatics.

Strikingly, the ne absorption spectrum of 2F-Phe -DPO-insulin is similar to that of wild- type human insulin, ting that the 2F-Phe modification does not prevent formation of a native-like dimer interface.

Structural odation of the 2F-PheB24 modification was analyzed in a monomeric context through 2D-NMR studies of 2F-PheBZ4-DKP-insulin. A native-like pattern of IH-NMR chemical shifts and nuclear Overhauser effects (NOEs) was observed; molecular models based on distance-geometry and simulated annealing were similar to those obtained in 2D-NMR studies of DKP-insulin. Additional ural studies were undertaken by single- crystal X-ray crystallography. Crystals based on zinc ulin hexamers were grown as described (Liu, M., Wan, Z., Chu, Y.C., Aladdin, H., Klaproth, B., Choguette, M., Hua, Q.X., Mackin, R., Rao, J.S., De Meyts, P., Katsoyannis, P.G., Arvan, P. & Weiss, M.A. (2009) The crystal structure of a “nonfoldable” insulin: impaired folding efficiency despite native ty. J.

Biol. Chem. 284, 35259-35272). The structures are similar to those of the parent analogue as illustrated in Figure 10. In particular, the inward orientation of the 2F-Phe aromatic ring with respect to an individual insulin protomer leaves a native-like outer dimerization interface.

Irrespective of theory, this inward orientation was also ed in 2D-NMR studies of the monomeric 2F-Phe1324—DKP-insulin analogue and is likely to accrue favorable electrostatic ctions, thereby rationalizing the increased thermodynamic ities of 2F-Phe1324 insulin analogues.

Dissociation constants (Kd) were determined as described by Whittaker and Whittaker (2005. J Biol. Chem. 280: 20932—20936), by a competitive displacement assay using 125I—TyrAM— insulin (kindly provided by Novo—Nordisk) and the purified and solubilized insulin receptor (isoforrn B or A) in a microtiter plate antibody capture assay with minor modification; transfected receptors were tagged at their C-terminus by a triple repeat of the FLAG epitope (DYKDDDDK) and microtiter plates were coated by anti-FLAG M2 onal antibody (Sigma). The percentage of tracer bound in the e of ing ligand was less than 15% to avoid ligand—depletion artifacts. g data (illustrated in Fig. 5) were analyzed by non- linear sion using a heterologous competition model (Wang, 1995, FEBS Lett. 360: 111- l 14) to obtain dissociation constants. Results are ed in Table 2 (2F—Phe1324 KP—insulin analogue ve to KP-insulin) and Table 3 (templates DKP, DDP, and DPO; see footnote to Table 3); dissociation constants are provided in units of nanomolar. (The two studies were conducted on different dates with different preparations of insulin receptor (IR isoform B; IR-B) and IGF receptor (IGF-IR) and so are tabulated independently.) The 2F-Phe1324 modification of KP-insulin reduces IR-B receptor-binding affinities by between twofold and threefold; such small reductions are typically associated with native or near-native ycemic potencies in vivo as demonstrated herein in diabetic Lewis rats. No significant increase was observed in the cross-binding of B24-KP-insulin to IGF-IR. The 2F-PheB24 modification of DKP-insulin s IR-B receptor-binding affinities by less than d; a trend toward increased cross- binding to IGF—IR was observed near the limit of tical significance.

Table 2 Binding of Insulin Analogues to Insulin Receptor and IGF Receptor Protein IR—B binding IGF-1R binding insulin 0.063 a: 0.014 nM 5.6 i 0.9 nM KP-insulin 0.062 d: 0.011 nM 8.2 d: 1.2 nM 2F-PheBz4-KP-insulin 0.472 a: 0.011 nM 34.1 i 1.2 nM IR-B, B isoform of the insulin receptor; , Type 1 IGF receptor Table 3 Binding of Insulin Analogues to Insulin Receptor and IGF Receptor Protein lR-B binding IGF-1R binding A. DKP Template Insulin* 0.063 i 0.014 nM 5.6 :l: 0.9 nM sulin 0.020 1 0.003 nM 1.8 i 0.3 nM 2F-PheB24—DKP-insulin 0.131 i 0.020 nM 9.2 :1: 1.2 nM B. DDP Template insulin 0.059 i 0.010 nM 3.7 i 0.6 nM KP-insulin 0.064 i 0.009 nM 6.2 i 1.2 nM 2F—PheBz4-DDP-insulin 0.063 a: 0.010 nM 4.8 i 0.8 nM C. DPO Template insulin 0.048 :I: 0.008 nM 3.1 :I: 0.5 nM AspBIO-OmBzg—insulin 0.020 a: 0.014 nM 1.2 :I: 0.2 nM 2F—PheBz4-DPO-insulin 0.082 i 0.012 nM 4.0 i 0.6 nM IR-B, B isoform of the insulin receptor. *, Value ed from Table 2.

The binding affinities of analogues containing the non-standard amino acid Omithine at position B29 were similarly tested, both with and without a 2F—Phe substitution at B24.

Results are provided in Table 3 as dissociation nts relative to the human insulin receptor isofonn B (th—B), and human IGF receptor (hIGFR). While Om1329 has similar binding affinities for each receptor as wild type insulin, NleB29 has a sed affinity for hIR-B and lGFR relative to wild type insulin. An analogue containing Om1329 in combination with 2F— PheB24, however, had decreased binding affinity for both isoforms of insulin receptor and slightly increased affinity for hIGFR. The 2F-PheB24, Nle1329 analogue had r binding affinity for hIGFR as the Nle1329 only analogue, but had decreased binding affinity for hIR-B.

Table 4 Thermodynamic Stabilities of Insulin Analogues n AGLl (kcal/mole) protein AG“ (kcal/mole) insulin 3.6 i 0.1 2F-insulinb ND ulin 2.8 i 0.1 2F-KP-insulin 3.6 i 0.1 DKP-insulin 4.3 i 0.1 2F-DKP-insulin 4.9 :I: 0.1 DDP—insulin NDa 2F-DDP-insulin 4.7 i 0.1 OmBzg-insulin ND£1 2F-OrnBZ9-insulin 4.0 i 0.1 DPO—insulin NDa 2F-DPO-insulin 5.0 i 0.1 21Free energies of unfolding (DGu) were inferred from CD-detected ine ration studies based on application of a ate model. ND, not determined. b2F designates the ation 2F—Phe1324 in 1324 insulin (also designated ortho—monofluoro-Phe ). Analogue abbreviations: DDP, substitutions [AspB'0, AspBZS, ProBZg]; DKP, substitutions [AspB]0, LysBzS, ProBzg]; DPO, substitutions [AspB'0, Ornmg] with Pro at position B28 as in wild-type insulin; KP, substitutions S, ProBzg]; and Orn, ornithine.

A method for treating a patient comprises administering an n analogue 824 modification containing a 2F-Phe or additional acid substitutions in the A or B chain as known in the art or described herein. In one example, the 2F-Phe1324 tuted insulin analogue is an insulin analogue containing 2F-Phe at position B24 in the context of DKP—insulin. In another example, 2F-Phe is substituted within AspBlO-human insulin ues containing non—standard modifications at position B29 (Omithine or Norleucine). It is yet another aspect of the present invention that use of non-standard amino-acid substitutions enables a rapid and efficient method of preparation of insulin analogues by trypsin-mediated semi—synthesis using unprotected octapeptides.

In still another example, the insulin analogue is administered by an external or implantable insulin pump. An insulin analogue of the present invention may also contain other modifications, such as a tether between the inus of the B chain and the N-terminus of the A chain as described more fully in US. Patent No. 8,192,957.

A pharamaceutical composition may comprise such insulin analogues and which may optionally include zinc. Zinc ions may be included in such a ition at a level of a molar ratio of between 2.2 and 3.0 per hexamer of the insulin analogue. In such a formulation, the concentration of the insulin analogue would typically be between about 0.1 and about 3 mM; trations up to 3 mM may be used in the oir of an insulin pump. Modifications of meal-time insulin analogues may be formulated as described for (a) “regular” formulations of Humulin® (Eli Lilly and C0,), g® (Eli Lilly and Co.), Novalin® (Novo-Nordisk), and Novalog® Nordisk) and other rapid—acting insulin formulations currently approved for human use, (b) “NPH” formulations of the above and other insulin analogues, and (0) mixtures of such formulations.

Excipients may include glycerol, e, arginine, Tris, other buffers and salts, and anti—microbial preservatives such as phenol and meta-cresol; the latter preservatives are known to enhance the stability of the insulin hexamer. Such a ceutical composition may be used to treat a patient having diabetes mellitus or other medical condition by administering a physiologically effective amount of the composition to the patient. The insulin analogues of the present invention may be formulated in the absence of zinc ions and in the presence of 5-10 mM ethylenediaminetetraacetic acid (EDTA) or ethyleneglycoltetraacetic acid (EGTA). The latter ing agents are used in the absence of citrate ions.

A nucleic acid comprising a sequence that encodes a polypeptide encoding an insulin analogue containing a sequence encoding at least a B chain of insulin with an ortho-monofluoro- Phenylalanine at position B24 is also envisioned. This can be accomplished through the introduction of a stop codon (such as the amber codon, TAG) at position B24 in conjunction with a suppressor tRNA (an amber suppressor when an amber codon is used) and a corresponding tRNA synthetase, which incorporates a non—standard amino acid into a polypeptide in response to the stop codon, as previously described r, 1998, n Sci. 7:419-426; Xie et al., 2005, Methods. 36: 227-23 8). The particular sequence may depend on the preferred codon usage of a species in which the nucleic-acid sequence will be uced. The nucleic acid may also encode other modifications of wild-type insulin. The nucleic-acid sequence may encode a modified A- or B—chain sequence containing an unrelated substitution or extension ere in the polypeptide or modified proinsulin ues. The nucleic acid may also be a portion of an expression vector, and that vector may be inserted into a host cell such as a prokaryotic host cell like an E. coli cell line, or a eukaryotic cell line such as S. cereviciae or Pischia pastoris strain or cell line.

For example, it is oned that synthetic genes may be synthesized to direct the expression of a B-chain polypeptide in yeast Piscia is and other microorganisms. The nucleotide sequence of a B-chain polypeptide utilizing a stop codon at position B24 for the e of incorporating an ortho—monofluoro-Phenylalanine at that on may be either of the following or variants thereof: (a) with Human Codon Preferences: TTTGTGAACCAACACCTGTGCGGCTCACACCTGGTGGAAGCTCTCTACCTAGTGTGC GGGGAACGAGGCTAGTTCTACACACCCAAGACC (SEQ ID NO: 18) (b) with Pichia Codon ences: TTTGTTAACCAACATTTGTGTGGTTCTCATTTGGTTGAAGCTTTGTACTTGGTTTGTG GTGAAAGAGGTTAGTTTTACACTCCAAAGACT (SEQ ID NO: 19) Similarly, a full-length pro-insulin cDNA having human codon preferences and utilizing a stop codon at position B24 for the purpose of incorporating ortho-monofluoro- Phenylalanine at that position may have the sequence of SEQ ID NO: 20.

TTTGTGAACC AACACCTGTG CGGCTCACAC CTGGTGGAAG CTCTCTACCT AGTGTGCGGG GAACGAGGCT AGTTCTACAC ACCCAAGACC CGCCGGGAGG CAGAGGACCT GCAGGTGGGG CAGGTGGAGC GCGG CCCTGGTGCA GGCAGCCTGC AGCCCTTGGC CCTGGAGGGG TCCCTGCAGA AGCGTGGCAT TGTGGAACAA TGCTGTACCA GCATCTGCTC CCTCTACCAG CTGGAGAACT ACTGCAACTA G (SEQ ID NO: 20) Likewise, a full-length human sulin cDNA utilizing a stop codon at position B24 for the purpose of incorporating an ortho-monofluoro-Phenylalanine at that position and having codons preferred by P. pastoris may have the ce of SEQ ID NO: 21.

TTTGTTAACC AACATTTGTG TGGTTCTCAT TTGGTTGAAG CTTTGTACTT GGTTTGTGGT GAAAGAGGTT AGTTTTACAC TCCAAAGACT AGAAGAGAAG ATTT GCAAGTTGGT CAAGTTGAAT TGGGTGGTGG TCCAGGTGCT GGTTCTTTGC AACCATTGGC AGGT TCTTTGCAAA AGAGAGGTAT TGTTGAACAA TGTTGTACTT CTATTTGTTC TTTGTACCAA TTGGAAAACT ACTGTAACTA A (SEQ ID NO: 21) Other variants of these ces, encoding the same polypeptide sequence, are possible, given the synonyms in the genetic code.

Based upon the foregoing disclosure, it should now be apparent that insulin ues provided will carry out the objects set forth above. Namely, these insulin analogues, when ated under a broad range of protein concentrations from 0.6—3.0 mM (typically ponding to strengths U-100 to U—500 in the cases of wild—type insulin and prandial insulin analogues), will exhibit enhanced rates of tion from a subcutaneous depot and pharmacologic action in the regulation of blood glucose concentration while maintaining at least a fraction of the biological activity of wild-type insulin. Further, formulations whose rapid- acting pharmacokinetic and pharmacodynamic ties are maintained at concentrations of insulin analogue as high as 3.0 mM (U-500 strength) will provide enhanced utility in the safe and effective treatment of diabetes us in the face of marked insulin resistance. It is, therefore, to be understood that any variations evident fall within the scope of the d invention and thus, the selection of specific component elements can be determined without departing from the spirit of the invention herein disclosed and described.

The following literature is cited to demonstrate that the g and assay methods described herein would be tood by one of ordinary skill in the art.

Furter, R., 1998. Expansion of the genetic code: Site-directed p-fluoro-phenylalanine incorporation in Escherichia coli. Protein Sci. 72419—426.

Merrifield, R.B., Vizioli, L.D., and Boman, H.G. 1982. Synthesis of the antibacterial peptide cecropin A (1-33). Biochemistry 21: 5020-5031.

Mirmira, R.G., and Tager, HS. 1989. Role of the phenylalanine B24 side chain in ing insulin interaction with its receptor: Importance of main chain conformation. J Biol.

Chem. 264: 6349-6354.

Sosnick, T.R., Fang, X., and Shelton, V.M. 2000. Application of circular dichroism to study RNA folding transitions. Methods Enzymol. 317: 393-409.

Wang, Z.X. 1995. An exact mathematical expression for describing competitive biding of two different s to a protein molecule FEBS Lett. 360: 111-1 14.

Weiss, M.A., Hua, Q.X., Jia, W., Chu, Y.C., Wang, R.Y., and Katsoyannis, PG. 2000.

Hierarchiacal protein sign": insulin's intrachain disulfide bridge tethers a recognition a— helix. Biochemistry 39: 15429-15440.

Whittaker, J ., and Whittaker, L. 2005. terization of the functional insulin binding es of the full length insulin receptor. J Biol. Chem. 280: 20932-20936.

Xie, J. and Schultz, PG. 2005. An expanding c code. Methods. 36: 227—23 8.

Claims (20)

CLAIMS What is claimed is:

1. A ceutical formulation comprising insulin having a variant insulin B-chain ptide containing an ortho-monofluoro-Phenylalanine substitution at position B24 in relation to the sequence of human insulin, in combination with a substitution of an amino acid containing an acidic side chain at position B10 in relation to the sequence of human insulin selected from Aspartic Acid and Glutamic Acid, and a substitution at position B29 in relation to the sequence of human insulin, the substitution being selected from the group consisting of Glutamic Acid, Alanine, Norleucine, Aminobutyric acid, Aminopropionic acid, ne, Diaminobutyric acid, and Diaminopropionic acid, wherein the insulin is present at a concentration of between 0.6 mM and 3.0 mM.

The pharmaceutical formulation of claim 1, wherein the insulin is present at a tration of at least 2 mM.

The pharmaceutical formulation of claim 2, wherein the substitution at position B29 in relation to the sequence of human n is selected from the group consisting of cine, Aminobutyric acid, Aminopropionic acid, Omithine, Diaminobutyric acid, and Diaminopropionic acid.

The pharmaceutical ation of any one of claims 1—3, wherein the variant B chain additionally contains a substitution at position B28 in relation to the sequence of human insulin selected from the group consisting rtic Acid, Proline and Lysine.

The pharmaceutical formulation of any one of claims 1, 2 or 4, wherein the t B chain ns a Glutamic Acid substitution at position B29 in relation to the sequence of human insulin.

The pharmaceutical formulation of any one of claims 1—3, wherein the variant B chain also contains a Lysine substitution at position B3 in relation to the sequence of human insulin.

The pharmaceutical ation of claim6, comprising SEQ ID NO: 8.

The pharmaceutical formulation of any one of claims 1-7, wherein the insulin is an analogue ofa mammalian insulin.

The pharmaceutical ation of claim 8, wherein the mammalian insulin is an analogue of human insulin.

10. The pharmaceutical formulation of claim I, wherein the B—chain polypeptide comprises an acid sequence selected from the group consisting of SEQ ID NOS: 5 and 8 and additionally comprising an A-chain polypeptide sequence having an amino—acid sequence of SEQ ID NO: 9.

ll. The pharmaceutical formulation of any one of claims l—lO, comprising an insulin A- chain polypeptide sequence containing a Glutamic acid substitution at position A8.

12. The ceutical formulation of any one of claims 1-10, comprising an insulin A- chain polypeptide sequence containing a Histidine substitution at position A8.

13. An n analogue or a physiologically acceptable salt thereof, wherein the insulin analogue or a physiologically acceptable salt thereof, wherein the insulin analogue or a physiologically acceptable salt thereof contains a variant B-chain polypeptide incorporating an ortho-monofluoro-Phenylalanine at position B24 and an Aspartic acid or ic acid tution at position B10, and a substitution at position B29 in relation to the sequence of human insulin, the substitution being ed from the group consisting of Glutamic Acid, Alanine, Norleucine, Aminobutyric acid, ropionic acid, Ornithine, Diaminobutryic acid, and opropionic acid, wherein the insulin analogue or a physiologically acceptable salt thereof is present at a concentration of between 0.6 mM and 3.0 mM, for the treatment of elevated blood sugar.

14. The insulin analogue or a physiologically acceptable salt thereof of claim 13, wherein the insulin analogue or a physiologically acceptable salt thereof is present at a concentration of at least 2 mM.

15. The insulin analogue or a logically able salt thereofof claim 13 or 14, wherein the substitution at position B29 in relation to the sequence of human insulin is selected from the group consisting of Norleucine, Aminobutyric acid, Aminopropionic acid, Ornithine, Diaminobutyric acid, and Diaminopropionic acid.

16. The insulin analogue or a physiologically acceptable salt thereof of any one of claims 13- 14, wherein the variant B chain contains a Glutamic Acid substitution at position B29 in relation to the sequence of human insulin.

17. A polypeptide comprising a variant insulin B-chain polypeptide sequence containing an ortho-monofluoro-Phenylalanine substitution at position B24 in relation to the ce of human n, in combination with a substitution of an amino acid containing an acidic side chain at position B10 in on to the sequence of human insulin, and a tution at position B29 in relation to the ce of human n selected from the group consisting of Glutamic Acid, Alanine, Ornithine, Diaminobutyric acid, Diaminopropionic acid, Norleucine, Aminobutyric acid, and Aminopropionic acid.

18. The polypeptide of claim 17, wherein the polypeptide is a proinsulin analogue or single- chain insulin analogue.

19. The polypeptide of claim 17 or claim 18, wherein the polypeptide contains a Glutamic Acid substitution at position B29 in relation to the sequence of human n.

20. The polypeptide of any one of claims 17-19, wherein the polypeptide additionally contains a Lysine substitution at position B3 in relation to the sequence of human insulin.