EP3419987A1 - Affinity ligand for the purification of glycosylated biomolecules - Google Patents
Affinity ligand for the purification of glycosylated biomoleculesInfo
- Publication number
- EP3419987A1 EP3419987A1 EP16706352.8A EP16706352A EP3419987A1 EP 3419987 A1 EP3419987 A1 EP 3419987A1 EP 16706352 A EP16706352 A EP 16706352A EP 3419987 A1 EP3419987 A1 EP 3419987A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- group
- compound
- acid
- alkyl
- aryl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H15/00—Compounds containing hydrocarbon or substituted hydrocarbon radicals directly attached to hetero atoms of saccharide radicals
- C07H15/20—Carbocyclic rings
- C07H15/203—Monocyclic carbocyclic rings other than cyclohexane rings; Bicyclic carbocyclic ring systems
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D15/00—Separating processes involving the treatment of liquids with solid sorbents; Apparatus therefor
- B01D15/08—Selective adsorption, e.g. chromatography
- B01D15/26—Selective adsorption, e.g. chromatography characterised by the separation mechanism
- B01D15/38—Selective adsorption, e.g. chromatography characterised by the separation mechanism involving specific interaction not covered by one or more of groups B01D15/265 - B01D15/36
- B01D15/3804—Affinity chromatography
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
- B01J20/281—Sorbents specially adapted for preparative, analytical or investigative chromatography
- B01J20/286—Phases chemically bonded to a substrate, e.g. to silica or to polymers
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
- B01J20/30—Processes for preparing, regenerating, or reactivating
- B01J20/32—Impregnating or coating ; Solid sorbent compositions obtained from processes involving impregnating or coating
- B01J20/3231—Impregnating or coating ; Solid sorbent compositions obtained from processes involving impregnating or coating characterised by the coating or impregnating layer
- B01J20/3242—Layers with a functional group, e.g. an affinity material, a ligand, a reactant or a complexing group
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
- B01J20/30—Processes for preparing, regenerating, or reactivating
- B01J20/32—Impregnating or coating ; Solid sorbent compositions obtained from processes involving impregnating or coating
- B01J20/3231—Impregnating or coating ; Solid sorbent compositions obtained from processes involving impregnating or coating characterised by the coating or impregnating layer
- B01J20/3242—Layers with a functional group, e.g. an affinity material, a ligand, a reactant or a complexing group
- B01J20/3244—Non-macromolecular compounds
- B01J20/3246—Non-macromolecular compounds having a well defined chemical structure
- B01J20/3248—Non-macromolecular compounds having a well defined chemical structure the functional group or the linking, spacer or anchoring group as a whole comprising at least one type of heteroatom selected from a nitrogen, oxygen or sulfur, these atoms not being part of the carrier as such
- B01J20/3255—Non-macromolecular compounds having a well defined chemical structure the functional group or the linking, spacer or anchoring group as a whole comprising at least one type of heteroatom selected from a nitrogen, oxygen or sulfur, these atoms not being part of the carrier as such comprising a cyclic structure containing at least one of the heteroatoms nitrogen, oxygen or sulfur, e.g. heterocyclic or heteroaromatic structures
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
- B01J20/30—Processes for preparing, regenerating, or reactivating
- B01J20/32—Impregnating or coating ; Solid sorbent compositions obtained from processes involving impregnating or coating
- B01J20/3231—Impregnating or coating ; Solid sorbent compositions obtained from processes involving impregnating or coating characterised by the coating or impregnating layer
- B01J20/3242—Layers with a functional group, e.g. an affinity material, a ligand, a reactant or a complexing group
- B01J20/3244—Non-macromolecular compounds
- B01J20/3265—Non-macromolecular compounds with an organic functional group containing a metal, e.g. a metal affinity ligand
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H23/00—Compounds containing boron, silicon, or a metal, e.g. chelates, vitamin B12
Definitions
- the present invention relates to a compound.
- Said compound may be used as a ligand in order to bind and purify glycosylated biomolecules.
- the present invention further relates to a complex comprising said compound and a Lewis-acidic transition metal ion or to a complex comprising said compound and boric acid or diboronic acid.
- the present invention also relates to methods for producing an affinity matrix for the purification of glycosylated biomolecules.
- the present invention relates to an affinity matrix obtainable by said methods.
- Affinity media containing protein ligands have long been employed in the purification of biomolecules.
- One key limitation of current affinity media equipped with protein ligands is diffusive mass transfer.
- the principle factor restricting the overall rate of glycoprotein adsorption to an affinity column is the rate of diffusion of the targeted adsorbate from the particle surface to its adsorption sites within the porous structure of the particle.
- macromolecules such as therapeutic glycoproteins
- these limitations of diffusive mass transfer are especially enhanced when the ligand employed is itself a macro molecule such as protein A, an antibody or another protein molecule.
- Protein A itself occupies a large amount of intrapore space in porous media and the presence of this large ligand within the porous structure of the matrix hinders diffusion of monoclonal antibody (mAb) adsorbate molecules to their binding sites.
- the dynamic binding capacities (DBCs) of current protein A resins and other affinity media with protein ligands are still too low to allow for sufficiently short enough processing times. Due to non-equilibrium mass transfer effects in the porous resin, dynamic binding capacity decreases with increasing concentration of the target glycoprotein at short residence times.
- protein-based affinity ligands contribute to a limitation of binding capacity that is not present with small molecule affinity ligands.
- Another major issue of multivalent protein-affinity ligands is the need for denaturing elution conditions.
- the strong multivalent binding between ligand and target protein typically requires harsh elution conditions such as a low pH shift where the protein ligands are denatured to perturb the steric fit and release the bound protein target.
- harsh elution conditions such as a low pH shift where the protein ligands are denatured to perturb the steric fit and release the bound protein target.
- denaturing affinity-elution steps can suffer from decreased product recovery. While limited product losses may be tolerated from a commercial point of view, the root cause for product losses in affinity/elution steps is a major issue of concern, namely the formation of undesirable product aggregates.
- Product aggregates in parenteral drug formulations compromise not only drug efficacy but also drug safety mainly by their potential to trigger immunogenic reactions with life-threatening consequences.
- the plain and simple adsorption of a glycoprotein at interfaces can induce physical instability and the formation of structurally altered protein and peptide molecules which may serve as nucleation precursors for the formation of aggregated seeds that can then serve as heterogeneous nuclei that foster protein aggregation.
- Rising protein concentration itself is yet another well-known trigger of aggregation.
- Target protein concentrations in a typical upstream harvest bulk range from 1 to 7 mg/ml. But once a protein has bound to a resin, local concentrations can rise to a level equivalent to resin capacity.
- any protein-based affinity ligand is gradually leached from the affinity matrix. Trace levels of leached protein ligand that co-elute with the target protein from the affinity matrix must be removed at later steps in the purification process making sure that leached ligand is no longer detectable in the purified drug substance. Protein A leachables are particularly dangerous.
- the protein A affinity ligand is derived from a type I membrane protein of the human-pathogenic bacterium Staphylococcus aureus and thus is a potential danger to patient safety.
- mAbs and Fc fusion proteins are typically administered parenterally and thus any contamination with Staphylococcus aureus protein A, a known superantigenic virulence factor, may be expected to cause an immediate and powerful immune response towards protein A. Moreover, protein A has also been suspected of an intrinsic mitogenic activity. In light of this, EMA and FDA regulatory authorities require documented evidence of leached protein A clearance during bioprocessing of mAbs and Fc fusion proteins intended for human use. Biopharmaceuticals intended for clinical administration must be monitored precisely to the parts-per-million (ppm) level for leached protein A contamination during in-process controls and release analytics for bulk drug substance.
- ppm parts-per-million
- Said ligands should offer the following advantages over the current state-of-the-art: (1) they should allow product capture and elution at constant pH so as to avoid triggering of process induced product aggregation, (2) they should enable higher ligand densities per matrix surface area and better diffusive mass transfer properties resulting in optimized breakthrough dynamics and increased dynamic binding capacities at high-flow rates, (3) they should be chemically and physically stable to last a maximum number of re-uses, and (4) they should be non-toxic and non-immunogenic when possibly co-eluted as leachables.
- the inventor of the present invention provides such ligands (compounds).
- the ligands of the present invention allow product capture and elution at constant pH, i.e. without pH shift, and, thus, avoid the formation of undesirable product aggregation.
- the ligands according to the present invention are further of low molecular weight and size and are able to bind to glycostructures, e.g. N-glycans, with a selectivity greater than that of monovalent boric and boronic acids. They are, thus, very suitable for the purification of glycosylated biomolecules.
- the ligands according to the present invention are based on a partial structure common to natural human N-glycans and are, therefore, expected to be non-toxic and non-immunogenic. All these attributes render the ligands of the present invention as attractive candidates, especially for cost-effective large-scale purification of glycoproteins and enveloped viruses comprising glycostructures on their surface.
- the present invention relates to a compound according to formula (I)
- A is either absent or is selected from the group consisting of alkyl, alkenyl, cycloalkyl, cycloalkenyl, aryl, arylalkyl, alkylaryl, heteroalkyl, heteroalkenyl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, heteroarylalkyl, arylheteroalkyl, heteroarylheteroalkyl, heteroalkylaryl, alkylheteroaryl, heteroalkylheteroaryl, alkoxy, alkenoxy, cycloalkoxy, cycloalkenoxy, aryloxy, arylalkoxy, and alkylaryloxy;
- X is a functional group that allows the covalent coupling of the compound to a solid support
- R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , and R 10 are independently from each other selected from the group consisting of H, -OH, (Ci-C6)alkoxy, and R n -C(0)-0-, wherein R 11 is H or (Ci-C 4 )alkyl;
- the present invention relates to a complex comprising:
- the present invention relates to a complex comprising: (a) the compound according to the first aspect; and
- the present invention relates to a method of producing an affinity matrix for the purification of glycosylated biomolecules, comprising the steps:
- step (iii) optionally contacting the functionalized solid support produced in step (ii)
- the present invention relates to a method of producing an affinity matrix for the purification of glycosylated biomolecules, comprising the steps:
- the present invention relates to an affinity matrix obtainable by the method according to the fourth or fifth aspect.
- the present invention relates to the use of the compound according to the first aspect, the complex according to the second or third aspect, or the affinity matrix according to the sixth aspect for the purification of glycosylated biomolecules.
- the present invention relates to a method for purifying glycosylated biomolecules from a cell culture supernatant comprising the steps of:
- the present invention relates to a method for purifying glycosylated biomolecules from a cell culture supernatant comprising the steps of:
- the terms used herein are defined as described in "A multilingual glossary of biotechno logical terms: (IUPAC Recommendations)", Leuenberger, H.G.W, Nagel, B. and Kolbl, H. eds. (1995), Helvetica Chimica Acta, CH-4010 Basel, Switzerland).
- oligopeptide refers to a short peptide- linked chain of amino acids, e.g. one that is typically less than about 50 amino acids long and more typically less than about 30 amino acids long. Said short peptide-linked chain of amino acids is typically more than about 2 amino acids long.
- fusion protein refers to a polypeptide comprising a polypeptide or polypeptide fragment coupled to heterologous amino acid sequences. Fusion proteins are useful because they can be constructed to contain two or more desired functional elements from two or more different proteins.
- each heavy chain contains a single site for N-linked glycosylation at an asparagine residue linking an N-glycan to the antibody molecule, usually at residue Asn-297 (Kabat et al, Sequence of proteins of immunological interest, Fifth Ed., U.S. Department of Health and Human Services, NIH Publication No. 91-3242). Included within the scope of the term are classes of Igs, namely, IgG, IgA, IgE, IgM, and IgD.
- IgGs are subtypes of IgGs, namely, IgGl, IgG2, IgG3 and IgG4.
- the terms are used in their broadest sense and include monoclonal antibodies (including full length monoclonal antibodies), polyclonal antibodies, single chain antibodies, and multispecific antibodies (e.g. bispecific antibodies).
- antibody fragment refers to a fragment of an antibody that contains at least the portion of the CH2 domain of the heavy chain immunoglobulin constant region which comprises an N-linked glycosylation site of the CH2 domain and is capable of specific binding to an antigen, i.e. chains of at least one VL and/or VH-chain or binding part thereof.
- Fc domain and “Fc region”, as used herein, refer to a C-terminal portion of an antibody heavy chain that interacts with cell surface receptors called Fc receptors and some proteins of the complement system. This property allows antibodies to activate the immune system.
- glycosylated bio molecules refers to molecules including large macro molecules such as proteins or lipids that contain oligosaccharide chains (glycans).
- glycoproteins refers to proteins that contain oligosaccharide chains (glycans) covalently attached to their polypeptide side-chains.
- the carbohydrate is attached to the protein in a co-translational or posttranslational modification. This process is known as glycosylation such as N-glycosylation or O-glycosylation.
- glyco lipids refers to carbohydrate-attached lipids. They occur where a carbohydrate chain is associated with phospholipids on the exoplasmic surface of the cell membrane. The carbohydrates are found on the outer surface of all eukaryotic cell membranes.
- glycolipid The carbohydrate structure of the glycolipid is controlled by the glycosyltransferases that add the lipids and glycosylhydrolases that modify the glycan after addition. Glyco lipids also occur on the surface of enveloped viruses including those used as attenuated life vaccines.
- glycostructure encompasses glycoproteins and/or glycooligopeptides that contain oligosaccharide chains (glycans) covalently attached to their polypeptide/oligopeptide side-chains.
- the carbohydrate is attached to the structure in a co-translational or posttranslational modification. As mentioned above, this process is known as glycosylation such as N-glycosylation or O-glycosylation.
- N-glycosylation means the addition of sugar chains which to the amide nitrogen on the side chain of asparagine.
- O-glycosylation means the addition of sugar chains on the hydroxyl oxygen on the side chain of hydroxylysine, hydroxyproline, serine, or threonine.
- N-glycan means an N-linked polysaccharide or oligosaccharide.
- An N-linked oligosaccharide is for example one that is or was attached by an N- acetylglucosamine residue linked to the amide nitrogen of an asparagine residue in a protein.
- the predominant sugars found on N-glycoproteins are glucose, galactose, mannose, fucose, N- acetylgalactosamine (GalNAc), N-acetylglucosamine (GlcNAc) and sialic acid (e.g., N-acetyl- neuraminic acid (NANA)).
- N-glycans have a common pentasaccharide core of Man 3 GlcNAc 2 ("Man” refers to mannose; “Glc” refers to glucose; and “NAc” refers to N-acetyl; GlcNAc refers to N-acetylglucosamine).
- N-glycans differ with respect to the number of branches (antennae) comprising peripheral sugars (e.g., GlcNAc, galactose, fucose and sialic acid) that are added to the Man3GlcNAc 2 core structure which is also referred to as the "trimannose core", the "pentasaccharide core” or the “paucimannose core”.
- branches comprising peripheral sugars (e.g., GlcNAc, galactose, fucose and sialic acid) that are added to the Man3GlcNAc 2 core structure which is also referred to as the "trimannose core", the "pentasaccharide core” or the "paucimannose core”.
- N- glycans are classified according to their branched constituents (e.g., high mannose, complex or hybrid).
- high mannose type N-glycan means an N-linked polysaccharide or oligosaccharide which has five mannose residues (Man 5 ), or more mannose residues (e.g. Mane, Man 7 , or Mans).
- complex type N-glycan means a N-linked polysaccharide or oligosaccharide which typically has at least one GlcNAc attached to the 1 ,3 mannose arm and at least one GlcNAc attached to the 1,6 mannose arm of a "trimannose" core.
- Complex N-glycans may also have galactose (“Gal”) or N-acetylgalactosamine (“GalNAc”) residues that are optionally modified with sialic acid or derivatives (e.g., "NANA” or "NeuAc", where “Neu” refers to neuraminic acid and "Ac” refers to acetyl).
- Complex N-glycans may also have intrachain substitutions comprising "bisecting" GlcNAc and core fucose ("Fuc").
- Complex type N-glycans in the context of the present invention may contain zero (GO), one (Gl), or two (G2) galactoses as well as one fucose attached to the first GlcNAc on the reducing end (denoted as GOF, GIF, G2F, respectively).
- hybrid type N-glycan means a N-linked polysaccharide or oligosaccharide which has at least one GlcNAc on the terminal of the 1,3 mannose arm of the trimannose core and zero or more mannoses on the 1,6 mannose arm of the trimannose core.
- paucimannose type N-glycan means small oligomannose N- glycans as they are commonly found in plants and invertebrates and having the composition Man 3 - 4 GlcNAc2.
- O-glycan means an O-linked polysaccharide or oligosaccharide.
- O-linked glycans are usually attached to the peptide chain through serine or threonine residues.
- O-linked glycosylation is a true post-translational event which occurs in the Golgi apparatus and which does not require a consensus sequence and no oligosaccharide precursor is required for protein transfer.
- the most common type of O-linked glycans contain an initial GalNAc residue (or Tn epitope), these are commonly referred to as mucin-type glycans.
- O-linked glycans include glucosamine, xylose, galactose, fucose, or mannose as the initial sugar bound to the Ser/Thr residues.
- O-Linked glycoproteins are usually large proteins (> 200 kDa) that are commonly biantennary with comparatively less branching than N-glycans.
- enveloped viruses comprising glycostructures on their envelopes
- the envelopes typically are derived from portions of the host (phospholipids and proteins), but include some (viral) glycostructures such as glycoproteins and/or glycooligopeptides. Functionally, viral envelopes help viruses to enter host cells and may help them to avoid the host immune system.
- (Viral) glycostructures such as glycoproteins and/or glycooligopeptides on the surface of the envelopes serve to identify and bind to receptor sites on the host's membrane. The viral envelope then fuses with the host's membrane, allowing the capsid and viral genome to enter and infect the host.
- the influenza virus and many animal viruses are enveloped viruses.
- the term "functional group”, as used herein, means any specific group of atoms and bonds within a larger molecule that is responsible for the characteristic chemical reactions of this molecule.
- the term “functional group that allows the covalent coupling of the compound”, as used herein, means a specific group of atoms and bonds within a larger molecule that renders the larger molecule reactable with another specific chemical or functional group so that a covalent bond is formed between these two molecules.
- Suitable functional groups include halide (CI, Br, F or I), hydroxyl, alkoxy (i.e.— OR where e.g.
- R alkyl C1-C30), carbonyl, carboxyl, anhydride, methacryl, epoxide, vinyl, nitrile, nitro, sulfate, sulfonyl, mercapto, sulfide, amino, amine, imine, amide and imide.
- Coupling reactions include all bioconjugation techniques known to someone skilled in the art including but not limited to N-hydroxysuccinimide-amino coupling, isocyanate-amino coupling, isothiocyanate-amino coupling, maleimide-sulfhydryl- coupling, azide-mediated Staudinger ligation, Huisgen Cyclization of Azides, Huisgen Sharpless Meldal azide-alkyne click chemistry, Suzuki coupling, Buchwald-Hartwig reaction, etc.
- alkyl refers to a saturated straight or branched carbon chain.
- the chain comprises from 1 to 30 carbon atoms, i.e. 1 , 2, 3, 4, 5, 6, 7, 8, 9, 10, 1 1 , 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, or 30, e.g. methyl, ethyl propyl, iso-propyl, butyl, iso-butyl, sec-butyl, tert-butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl, or dodecyl.
- the alkyl groups are optionally substituted.
- heteroalkyl refers to a saturated straight or branched carbon chain.
- the chain comprises from 1 to 30 carbon atoms, i.e. 1 , 2, 3, 4, 5, 6, 7, 8, 9, 10, 1 1 , 12, 13, 14, 15, 16, 17, 18, 19, 20, 21 , 22, 23, 24, 25, 26, 27, 28, 29, or 30, e.g.
- heteroatoms are selected from O, S, and N, e.g.
- heteroalkyl refers to -0-CH 3 , -OC 2 H 5 , -CH 2 -0-CH 3 , -CH 2 -0-C 2 H 5 , -CH 2 -0-C 3 H 7 , -CH2-O-C4H9, -CH 2 -0-C 5 Hi i, -C 2 H 4 -0-CH 3 , -C 2 H4-0-C 2 H 5 , -C 2 H 4 -0-C 3 H 7 , - C2H4-O-C4H9 etc.
- Heteroalkyl groups are optionally substituted.
- cycloalkyl and “heterocycloalkyl”, as used herein, by themselves or in combination with other terms, represent, unless otherwise stated, cyclic versions of “alkyl” and “heteroalkyl”, respectively, with preferably 3, 4, 5, 6, 7, or 8 carbon atoms forming a ring, e.g. cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl etc.
- cycloalkyl and “heterocycloalkyl” are also meant to include bicyclic, tricyclic and polycyclic versions thereof.
- bicyclic, tricyclic or polycyclic rings are formed, it is preferred that the respective rings are connected to each other at two adjacent carbon atoms, however, alternatively the two rings are connected via the same carbon atom, i.e. they form a spiro ring system or they form "bridged" ring systems.
- heterocycloalkyl preferably refers to a saturated ring having five members of which at least one member is an N, O or S atom and which optionally contains one additional O or one additional N; a saturated ring having six members of which at least one member is an N, O or S atom and which optionally contains one additional O or one additional N or two additional N atoms; or a saturated bicyclic ring having nine or ten members of which at least one member is an N, O or S atom and which optionally contains one, two or three additional N atoms.
- Cycloalkyl and “heterocycloalkyl” groups are optionally substituted.
- a heteroatom can occupy the position at which the heterocycle is attached to the remainder of the molecule.
- cycloalkyl include cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, spiro[3,3]heptyl, spiro[3,4]octyl, spiro[4,3]octyl, spiro[3,5]nonyl, spiro[5,3]nonyl, spiro[3,6]decyl, spiro[6,3]decyl, spiro[4,5]decyl, spiro[5,4]decyl, bicyclo[2.2.1]heptyl, bicyclo[2.2.2]octyl, adamantyl, and the like.
- heterocycloalkyl examples include l-(l,2,5,6-tetrahydropyridyl), 1-piperidinyl, 2- piperidinyl, 3-piperidinyl, 4-morpholinyl, 3-morpholinyl, l,8-diazo-spiro[4,5]decyl, 1,7-diazo- spiro[4,5]decyl, l,6-diazo-spiro[4,5]decyl, 2,8-diazo-spiro[4,5]decyl, 2,7-diazo-spiro[4,5]decyl, 2,6-diazo-spiro[4,5]decyl, l,8-diazo-spiro[5,4]decyl, 1,7 diazo-spiro[5,4]decyl, 2,8-diazo- spiro[5,4]decyl, 2,7-diazo-spiro[5,4]decyl, 3,8
- aryl preferably refers to an aromatic monocyclic ring containing 6 carbon atoms, an aromatic bicyclic ring system containing 10 carbon atoms or an aromatic tricyclic ring system containing 14 carbon atoms. Examples are phenyl, naphthyl, anthracenyl, or phenanthryl. The aryl group is optionally substituted.
- arylalkyl refers to an alkyl moiety, which is substituted by aryl, wherein alkyl and aryl have the meaning as outlined above.
- An example is the benzyl radical.
- the alkyl chain comprises from 1 to 24 carbon atoms, i.e. 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 , 12, 13, 14, 15, 16, 17, 18, 19, 20, 21 , 22, 23, or 24, e.g. methyl, ethyl, propyl, iso-propyl, butyl, iso-butyl, sec-butyl, tert-butyl, pentyl, hexyl, heptyl, octyl.
- arylalkyl group is optionally substituted at the alkyl and/or aryl part of the group.
- the aryl attached to the alkyl has the meaning phenyl, naphthyl, anthracenyl, or phenanthryl.
- arylalkyl can also be abbreviated to "aralkyl”.
- heteroaryl preferably refers to a five or six-membered aromatic monocyclic ring wherein at least one of the carbon atoms is replaced by 1, 2, 3, or 4 (for the five membered ring) or 1 , 2, 3, 4, or 5 (for the six membered ring) of the same or different heteroatoms, preferably selected from O, N and S; an aromatic bicyclic ring system with 8 to 12 members wherein 1, 2, 3, 4, 5, or 6 carbon atoms of the 8, 9, 10, 11 or 12 carbon atoms have been replaced with the same or different heteroatoms, preferably selected from O, N and S; or an aromatic tricyclic ring system with 13 to 16 members wherein 1, 2, 3, 4, 5, or 6 carbon atoms of the 13, 14, 15, or 16 carbon atoms have been replaced with the same or different heteroatoms, preferably selected from O, N and S.
- alkenyl and cycloalkenyl refer to olefmic unsaturated carbon atoms containing chains or rings with one or more double bonds. Examples are propenyl and cyclohexenyl.
- the alkenyl chain comprises from 2 to 30 carbon atoms, i.e. 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, or 30, e.g.
- the cycloalkenyl ring comprises from 3 to 8 carbon atoms, i.e. 3, 4, 5, 6, 7, or 8, e.g.
- heteroalkenyl and “heterocycloalkenyl”, as used herein, refer to unsaturated versions of “heteroalkyl” and “heterocycloalkyl”, respectively.
- heteroalkenyl refers to an unsaturated straight or branched carbon chain.
- the chain comprises from 2 to 30 carbon atoms, i.e. 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 , 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, or 30, which is interrupted one or more times, e.g. 1, 2, 3, 4, 5, with the same or different heteroatoms.
- the heteroatoms are selected from O, S, and N.
- R' is hydrogen or hydrocarbon (e.g. Ci to C 6 alkyl)
- Heteroalkenyl groups are optionally substituted.
- the term “heterocycloalkenyl” represents a cyclic version of "heteroalkenyl” with preferably 3, 4, 5, 6, 7, or 8 atoms forming a ring.
- heterocycloalkenyl is also meant to include bicyclic, tricyclic and polycyclic versions thereof. If bicyclic, tricyclic or polycyclic rings are formed, it is preferred that the respective rings are connected to each other at two adjacent atoms. These two adjacent atoms can both be carbon atoms; or one atom can be a carbon atom and the other one can be a heteroatom; or the two adjacent atoms can both be heteroatoms. However, alternatively the two rings are connected via the same carbon atom, i.e. they form a spiro ring system or they form "bridged" ring systems.
- heterocycloalkenyl preferably refers to an unsaturated ring having five members of which at least one member is an N, O or S atom and which optionally contains one additional O or one additional N; an unsaturated ring having six members of which at least one member is an N, O or S atom and which optionally contains one additional O or one additional N or two additional N atoms; or an unsaturated bicyclic ring having nine or ten members of which at least one member is an N, O or S atom and which optionally contains one, two or three additional N atoms.
- Heterocycloalkenyl groups are optionally substituted. Additionally, for heteroalkenyl and heterocycloalkenyl, a heteroatom can occupy the position at which the heterocycle is attached to the remainder of the molecule.
- alkylaryl refers to an aryl moiety that is substituted by alkyl, wherein aryl and alkyl have the meaning as outlined above.
- heteroarylalkyl refers to an alkyl moiety that is substituted by heteroaryl, wherein alkyl and heteroaryl have the meaning as outlined above.
- arylheteroalkyl refers to a heteroalkyl moiety that is substituted by aryl, wherein heteroalkyl and aryl have the meaning as outlined above.
- heteroarylheteroalkyl refers to a heteroalkyl moiety that is substituted by heteroaryl, wherein heteroalkyl and heteroaryl have the meaning as outlined above.
- heteroalkylaryl refers to an aryl moiety that is substituted by heteroalkyl, wherein aryl and heteroalkyl have the meaning as outlined above.
- alkylheteroaryl refers to a heteroaryl moiety that is substituted by alkyl, wherein heteroaryl and alkyl have the meaning as outlined above.
- heteroalkylheteroaryl refers to a heteroaryl moiety that is substituted by heteroalkyl, wherein heteroaryl and heteroalkyl have the meaning as outlined above.
- alkoxy refers to an alkyl-O- moiety, wherein alkyl has the meaning as outlined above.
- alkenoxy refers to an alkenyl-O- moiety, wherein alkenyl has the meaning as outlined above.
- cycloalkoxy refers to a cycloalkyl-O- moiety, wherein cycloalkyl has the meaning as outlined above.
- cycloalkenoxy refers to a cycloalkenyl-O- moiety, wherein cycloalkenyl has the meaning as outlined above.
- aryloxy refers to an aryl-O- moiety, wherein aryl has the meaning as outlined above.
- arylalkoxy refers to an arylalkyl-O- moiety, wherein arylalkyl has the meaning as outlined above.
- alkylaryloxy refers to an alkylaryl-O- moiety, wherein alkylaryl has the meaning as outlined above.
- the inventor of the present invention developed new ligands (compounds) based on specific coupling enabled derivatives of the branched oligosaccharide 3,6-Trimannose. These ligands are functionalized at the reducing end of the branching mannose with a functional group that can be used for position specific coupling of the branched 3,6-Trimannosyl-ligand to an affinity matrix.
- the present invention relates to a compound (ligand) according to formula
- A is either absent or is selected from the group consisting of alkyl, alkenyl, cycloalkyl, cycloalkenyl, aryl, arylalkyl, alkylaryl, heteroalkyl, heteroalkenyl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, heteroarylalkyl, arylheteroalkyl, heteroarylheteroalkyl, heteroalkylaryl, alkylheteroaryl, heteroalkylheteroaryl, alkoxy, alkenoxy, cycloalkoxy, cycloalkenoxy, aryloxy, arylalkoxy, and alkylaryloxy;
- X is a functional group that allows the covalent coupling of the compound to a solid support
- R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , and R 10 are independently from each other selected from the group consisting of H, -OH, (Ci-C6)alkoxy, and R n -C(0)-0-, wherein R 1 1 is H or (Ci-C4)alkyl, preferably R 1 1 is methyl;
- the inventor of the present invention found that the above compound (ligand) allows product capture and elution at constant pH, i.e. without pH shift, and, thus, avoids the formation of undesirable product aggregation.
- the above compound is further of low molecular weight and size and is able to bind to glycostructures, e.g. N-glycans, with a selectivity greater than that of monovalent boric and boronic acids. It is, thus, very suitable for the purification of glycosylated biomolecules.
- the above compound is based on a partial structure common to natural human N-glycans and is, therefore, expected to be non-toxic and non-immunogenic. The above compound is, thus, an attractive candidate, especially for cost-effective large-scale purification of glycoproteins and enveloped viruses comprising glycostructures on their surface.
- A is selected from the group consisting of (Ci-C3o)alkyl, (C 2 -C 3 o)alkenyl, (C 3 -C 8 )cycloalkyl, (C 3 -C 8 )cycloalkenyl, (C 6 -Ci 4 )aryl, (C 6 -Ci4)aryl(Ci-C 24 )alkyl, (Ci- C 24 )alkyl(C6-Ci 4 )aryl, (Ci-C 3 o)heteroalkyl, (C 2 -C 3 o)heteroalkenyl, (C 3 -C8)heterocycloalkyl, (C 3 - C8)heterocycloalkenyl, (C 3 -Ci 3 )heteroaryl, (C 3 -Ci 3 )heteroaryl(Ci-C 24 )alkyl, (C6-Ci 4 )aryl(Ci- C- C6
- X is selected from the group consisting of -OH, -N0 2 , -NH 2 , -COOH,
- -A-X together is selected from the group consisting of -C 6 H 4 -X, - CioH 6 -X,-Ci4H 8 -X, -0-C 6 H 4 -X, -O-CioHe-X, and -0-Ci 4 H 8 -X.
- X is selected from the group consisting of -OH, -NO2, -NH 2 , -COOH, -NCO, azlactone-, N-hydroxysuccinimide-, maleinimide, carboxamido-, alkynyl, -N3, and -SH.
- R 1 and R 2 are independently from each other selected from the group consisting of H, -OH, and -(Ci-Ce)alkoxy and/or that R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , and R 10 are -OH.
- the compound has a structure according to formula (II):
- L is selected from the group consisting of alkyl, alkenyl, cycloalkyl, cycloalkenyl, aryl, arylalkyl, alkylaryl, heteroalkyl, heteroalkenyl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, heteroarylalkyl, arylheteroalkyl, heteroarylheteroalkyl, heteroalkylaryl, alkylheteroaryl, and heteroalkylheteroaryl;
- X is a functional group that allows the covalent coupling of the compound to a solid support
- R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , and R 10 are independently from each other selected from the group consisting of H, -OH, (Ci-C6)alkoxy, and R n -C(0)-0-, wherein R 1 1 is H or (Ci-C4)alkyl, preferably R 1 1 is methyl.
- L is selected from the group consisting of (Ci-C3o)alkyl, (C 2 -C 3 o)alkenyl, (C 3 -C 8 )cycloalkyl, (C 3 -C 8 )cycloalkenyl, (C 6 -Ci 4 )aryl, (C 6 -Ci 4 )aryl(Ci-C 24 )alkyl, (Ci- C 24 )alkyl(C 6 -Ci 4 )aryl, (Ci-C 3 o)heteroalkyl, (C 2 -C 3 o)heteroalkenyl, (C 3 -C8)heterocycloalkyl, (C 3 - C8)heterocycloalkenyl, (C 3 -Ci 3 )heteroaryl, (C 3 -Ci 3 )heteroaryl(Ci-C 24 )alkyl, (C 6 -Ci 4 )aryl(
- X is selected from the group consisting of -OH, -N0 2 , -NH 2 , -COOH, -NCO, azlactone-, N-hydroxysuccinimide-, maleinimide, carboxamido-, alkynyl, -N 3 , and -SH.
- These functional groups are able to support stable coupling to a solid support by undergoing covalent chemical bonding.
- R 1 and R 2 are independently from each other selected from the group consisting H, -OH, and -(Ci-Ce)alkoxy and/or that R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , and R 10 are - OH.
- R 3 , R 4 and R 7 , R 8 are -OH.
- R 4 , R 5 and R 8 , R 9 are -OH.
- R 3 , R 4 and R 7 , R 8 are -OH.
- R 5 , R 6 and R 9 , R 10 are - OH.
- the compound (ligand) is 4-Aminophenyl-3,6-Trimannose. This compound (ligand) is shown in Figure 3.
- the compound according to the first aspect is capable of binding to the glycosylated biomolecules, e.g. glycoproteins, particularly to the glycostructures of the glycoproteins, gly co lipids, or glycostructures on the envelopes of enveloped viruses.
- the compound according to the first aspect is capable of binding to the pyranoid-diol functionality of said glycoproteins or glycostructures, preferably to the 1 ,2 cis-diol and/or 1 ,3 trans-diol functionality of said glycoproteins or glycostructures.
- the compound thus, allows the purification of glycosylated biomolecules from cell culture supernatants.
- the present invention relates to a complex comprising:
- the Lewis-acidic transition metal ion is selected from the group consisting of Cu(II), Mn(II), Fe(II), Fe(III), and Co(II).
- the present invention relates to a complex comprising: (a) the compound according to the first aspect; and
- the diboronic acid is selected from the group consisting of 1,4- phenylendiboronic acid (synm. 1,4-benzenediboronic acid), 2-Nitrobenzene-l,4-diboronic acid (synm. 2-nitro-l,4-phenylenediboronic acid), 2,2'-Bithiophene-5,5'-diboronic acid, 4-4'- biphenyldiboronic acid, 2,5-thiophenediboronic acid, stilbene-4,4-diboronic acid, 4,4'-oxybis(l,4- benzene)diboronic acid, dibenzofuran-4,6-diboronic acid and derivatives thereof.
- the complexes according to the second or third aspect are capable of binding to the glycosylated biomolecules, e.g. glycoproteins, particularly to the glycostructures of the glycoproteins, glyco lipids, or glycostructures on the envelopes of enveloped viruses.
- the complexes according to the second or third aspect are capable of binding to the pyranoid-diol functionality of said glycoproteins or glycostructures, preferably to the 1,2 cis-diol and/or 1,3 trans-diol functionality of said glycoproteins or glycostructures.
- the complexes thus, allow the purification of glycosylated biomolecules from cell culture supernatants.
- the present invention relates to a method of producing an affinity matrix for the purification of glycosylated biomolecules, comprising the steps:
- step (iii) optionally contacting the functionalized solid support produced in step (ii)
- the Lewis-acidic transition metal ion is selected from the group consisting of
- the diboronic acid is selected from the group consisting of ,4- phenylendiboronic acid (synm. 1,4-benzenediboronic acid), 2-Nitrobenzene-l,4-diboronic acid
- the solid support may be a membrane or a solid phase chromatographic support such as a resin or a monolith.
- the solid support may be in the format of a chromatography column or a membrane adsorber.
- the solid support may also be a bead, particularly a set of beads.
- the present invention relates to a method of producing an affinity matrix for the purification of glycosylated biomolecules, comprising the steps:
- the solid support may be a membrane or a solid phase chromatographic support such as a resin or a monolith.
- the solid support may be in the format of a chromatography column or a membrane adsorber.
- the solid support may also be a bead, particularly a set of beads.
- Covalent coupling as described in the above methods allows the formation of a very active and stable complex.
- the complex is permanently bound and will not desorb/leach over time, the elimination of "crosstalk" between the complexes permits multiplexed assays, the complexes are favorably presented on the surface of the bead such that binding moieties are available for interaction with the glycosylated biomolecules, and binding kinetics can approach those of solution-based binding.
- the present invention relates to an affinity matrix obtainable by the method according to the fourth or fifth aspect.
- the affinity matrix according to the sixth aspect is capable of binding to the glycosylated biomolecules, e.g. glycoproteins, particularly to the glycostructures of the glycoproteins, glycolipids, or glycostructures on the envelopes of enveloped viruses.
- the affinity matrix according to the sixth aspect is capable of binding to the pyranoid-diol functionality of said glycoproteins or glycostructures, preferably to the 1,2 cis-diol and/or 1,3 trans-diol functionality of said glycoproteins or glycostructures.
- the affinity matrix thus, allows the purification of glycosylated biomolecules from cell culture supernatants.
- the present invention relates to the use of
- glycosylated biomolecules are selected from the group consisting of (a) glycoproteins,
- the glycoproteins may be antibodies, antibody fragments, fusion proteins, virus proteins, virus protein fragments, antigens, cytokines, clotting factors, growth factors, enzymes, or hormones.
- the antibody or the antibody fragment is selected from the group consisting of IgG, preferably IgGl, IgG2, IgG3, IgG4, IgM, IgA, IgD and IgE.
- the fusion protein comprises the Fc region of an antibody, e.g. the Fc region of IgG, such as the Fc region of IgGl , IgG2, IgG3, IgG4, IgM, IgA, IgD or IgE.
- the cytokine is interferon or interleukin.
- the clotting factor is factor VII, factor IX, or factor VIII, in particular full-length and B-domain deleted versions thereof.
- the enzyme is a glucocerebrosidase, an iduronidase, arylsulfatase A and B, alpha-glucosidase, or iduronat-2-sulfatase.
- the hormone is a follicle stimulating hormone (FSH), luteinizing hormone (LH), chorionic gonadotropin (HCG), or a tyroid stimulating hormone (TSH).
- the virus proteins or virus protein fragments may be comprised in the envelope membrane of an enveloped virus.
- Said enveloped virus may be an influenza virus, a rabies virus, chikungunya virus, vaccinia virus including modified vaccinia ankara (MVA) virus, mumps virus, measles virus, canine distemper virus, or a peste desdriven ruminants virus (PPRV).
- the glycolipids may be glyceroglyco lipids, e.g. galactolipids, sulfolipids (SQDG), or glycosphingo lipids, e.g. cerebrosides, gangliosides, globosides, sulfatides or glycophosphosphingo lipids.
- the glycolipids may be comprised in the envelope membranes of enveloped viruses. Glycosphingolipids (GSL) are particularly preferred.
- Glycosphingo lipids contain a hydrophobic ceramide anchor N-acylsphingosine and a hydrophilic head-group composed of saccharides. They are normally found at the outer surface of cell membranes.
- the composition of the saccharide-moiety is cell type specific and depends on the developmental stage of the organism or can change with the oncogenic state of a cell.
- Said enveloped viruses may be influenza viruses, rabies viruses, chikungunya viruses, vaccinia viruses including modified vaccinia ankara (MVA) viruses, mumps viruses, measles viruses, canine distemper viruses, or peste despoor ruminants viruses (PPRV).
- MVA modified vaccinia ankara
- mumps viruses mumps viruses
- measles viruses canine distemper viruses
- PPRV despoorative ruminants viruses
- the glycosylated biomolecules carry N-glycans. It is even more preferred that the N-glycans are selected from the group consisting of high-mannose type N- glycans, complex type N-glycans, hybrid type N-glycans, and paucimannose type N-glycans.
- the N-glycans may be biantennary N-glycans of the hybrid type or biantennary N-glycans of the complex type.
- the present invention relates to a method for purifying glycosylated biomolecules from a cell culture supernatant comprising the steps of:
- the cell culture supernatant comprising glycosylated biomolecules is obtained from a cell culture.
- Techniques to harvest the cell culture supernatant from a cell culture are known to the skilled person. This can be done, for example, by centrifugation, sedimentation and/or filtration techniques.
- the cell culture supernatant may be a vertebrate cell culture supernatant, in particular a mammalian, a fish, an amphibian, a reptilian, or an avian cell culture supernatant.
- the mammalian cell culture supernatant is a human, hamster, canine, or monkey cell culture supernatant, preferably a Chinese hamster ovary (CHO) cell culture supernatant
- the fish cell culture supernatant is an Ictalurus punctatus (channel catfish) ovary (CCO) cell culture supernatant
- the amphibian cell culture supernatant is a Xenopus laevis kidney cell culture supernatant
- the reptilian cell culture supernatant is an Iguana iguana heart cell culture supernatant
- the avian cell culture supernatant is a duck cell culture supernatant.
- the method further comprises the step(s) of:
- the washing buffer may be any buffer which allows the removal of unspecific binding partners from the affinity matrix.
- standard phosphate buffered saline (PBS) may be used.
- the elution buffer may be any buffer which allows the release of the glycosylated biomolecules from the affinity matrix.
- standard PBS supplemented with fructose may be used.
- the competitive eluent may be any eluent which allows the displacement of the glycosylated biomolecules from the affinity matrix.
- the competitive eluent may be selected from the group consisting of furanoid cis diol sugars or glycosides, pyranoid 1,2,3 triol sugars or glycosides, sugar alcohols, e.g.
- sorbitol adonitol, mannitol, xylitol, dulcitol, pentaerythritol, or erythritol, alpha hydroxy carbonic acids, e.g. glycolate, lactate, malate, tartrate, citrate, alpha- hydroxy caprylate, salicylate or glucuronate, and hydroxylamino compounds, e.g. triethanolamin or Tris-hydroxymethyl-aminomethan (TRIS).
- TMS Tris-hydroxymethyl-aminomethan
- the present invention relates to a method for purifying glycosylated biomolecules from a cell culture supernatant comprising the steps of:
- the cell culture supernatant comprising glycosylated biomolecules is obtained from a cell culture.
- Techniques to harvest the cell culture supernatant from a cell culture are known to the skilled person. This can be done, for example, by centrifugation, sedimentation and/or filtration techniques.
- the cell culture supernatant may be a vertebrate cell culture supernatant, in particular a mammalian, a fish, an amphibian, a reptilian, or an avian cell culture supernatant.
- the mammalian cell culture supernatant is a human, hamster, canine, or monkey cell culture supernatant, preferably a Chinese hamster ovary (CHO) cell culture supernatant
- the fish cell culture supernatant is an Ictalurus punctatus (channel catfish) ovary (CCO) cell culture supernatant
- the amphibian cell culture supernatant is a Xenopus laevis kidney cell culture supernatant
- the reptilian cell culture supernatant is an Iguana iguana heart cell culture supernatant
- the avian cell culture supernatant is a duck cell culture supernatant.
- the method further comprises the step(s) of:
- the washing buffer may be any buffer which allows the removal of unspecific binding partners from the precipitate.
- washing buffer phosphate buffered saline (PBS) may be used.
- the elution buffer may be any buffer which allows the dissociation of the precipitate and, thus, the release of the glycosylated biomolecules from the precipitate. Thus, it may also be designated as dissociation buffer.
- elution buffer dissociation buffer
- phosphate buffered saline supplemented with fructose may be used.
- the competitive eluent may be any eluent which allows the displacement of the glycosylated biomolecules from the precipitate. It is further capable of dissociating the precipitate. Thus, it may also be designated as competitive dissociating reactant.
- the competitive eluent (competitive dissociating reactant) may be selected from the group consisting of furanoid cis diol sugars or glycosides, pyranoid 1,2,3 triol sugars or glycosides, sugar alcohols, e.g.
- sorbitol adonitol, mannitol, xylitol, dulcitol, pentaerythritol, or erythritol, alpha hydroxy carbonic acids, e.g. glycolate, lactate, malate, tartrate, citrate, alpha-hydroxy caprylate, salicylate or glucuronate, and hydroxylamino compounds, e.g. triethanolamin or Tris-hydroxymethyl-aminomethan (TRIS).
- TMS Tris-hydroxymethyl-aminomethan
- steps (ii), (iii), and/or (iv) of the methods of the eighth or ninth aspect are conducted at a pH between 6 and 8, more preferably at a pH between 6.5 and 7.5, even more preferably at a pH between 6.8 and 7.2, e.g. at a neutral pH (pH 7).
- a pH between 6 and 8 more preferably at a pH between 6.5 and 7.5, even more preferably at a pH between 6.8 and 7.2, e.g. at a neutral pH (pH 7).
- the washing and/or elution (dissociation) buffer has such a pH.
- the binding of the glycosylated biomolecules to the affinity matrix is performed at such a pH or that the precipitation of the glycosylated biomolecules from the cell culture supernatant is performed at such a pH.
- the skilled person is aware of techniques how to determine the purity of the glycosylated biomolecules such as glycoproteins or enveloped viruses.
- the purity of the glycoproteins is preferably measured using (i) spectrometry, preferably mass spectrometry (MS), (ii) chromatography, preferably liquid chromatography (LC), more preferably high performance liquid chromatography (HPLC), (iii) gel electrophoresis, preferably SDS gel electrophoresis, (iv) Westemblot/Immunoblot, or (v) combinations thereof.
- the chromatography preferably liquid chromatography (LC), more preferably high performance liquid chromatography (HPLC)
- spectrometry preferably mass spectrometry (MS).
- the purity of the purified glycoprotein is preferably measured using liquid chromatography-mass spectrometry (LC-MS) and is more preferably measured using high performance liquid chromatography-mass spectrometry (HPLC-MS).
- Figure 1 Schematic representation of a biantennary fucosylated G2F N-glycan, a complex glycan structure commonly found on therapeutic IgGl-type antibodies. Characteristic partial structures of complex N-glycan are highlighted in the dotted circles. The combination of fucosyl- chitobiose and 3,6-trimannose is termed "N-glycan core" structure.
- FIG. 2 Schematic representation of the synthesis of the compound (ligand) 4- Aminophenyl-3,6-Trimannose.
- PhC (OMe) 3 Trimethylorthobenzoate
- p-TsOH para- Toluenesulfonic acid
- TFA Trifluoroacetic acid
- BF 3 OEt 2 Boron tri- fluoride diethyl etherate
- OTCA Trichloroacetimidate-moiety
- Ac acetyl
- Bz Benzoyl
- MeOH Methanol
- NaOMe Sodium methoxide
- K 2 C0 3 Potassium carbonate.
- Figure 3 Schematic representation of the compound (ligand) 4-Aminophenyl-3,6- Trimannose.
- Figure 4 Schematic representation of hypothetical bivalent ligand binding: The borate charged 4-Aminophenyl-trimannosyl-ligand forms a tetradentate diester with the juxtaposed biantennary N-glycan of the target glycoprotein.
- FIG. 5 Schematic representation of hypothetical bivalent ligand binding: The proposed 4-Aminophenyl-trimannosyl ligand forms a bivalent metal coordination complex with the juxtaposed N-glycan of the target glycoprotein.
- coordination complex formation at C3/C4 hydroxyl groups is shown illustratively.
- the other remaining hydroxyl groups at C2 and C6 may as well support formation of coordination complexes with transition metal ions.
- M(II,III) symbolize Lewis-acidic transition metal ions.
- 4-Nitrophenyl mannoside 1 is treated with trimethylorthobenzoate and p-TsOH in acetonitrile to yield a bisorthoester, which is subsequently hydro lysed by exposure to aqueous trifluoroacetic acid to give the 2,4-di-O-benzoate 2 ( Figure 2).
- Bisglycosylation of diol 2 by treatment with boron tri- fluoride diethyl etherate and an excess of tetraacetyl-a-D-mannopyranoside trichloroacetimidate donor 3 then yields trisaccharide 4 in good yield.
- Unreacted glyoxal sites are blocked with 20 ⁇ of ethanolamine per every ml of glyoxal beads with 5 ml of water and the resultant solution is added to the ligand-coupled bead slurry and the reaction is allowed to proceed for 1 hour. Then the beads are washed on a filter funnel with at least 5 volumes of water or buffer (but not coupling buffer). The ligand-coupled glyoxal beads are stored in a preservative-containing phosphate buffer.
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