CN110982879A - LAMP hydrogen ion driven i-motif conversion ratio type electrochemical sensor and construction method - Google Patents

LAMP hydrogen ion driven i-motif conversion ratio type electrochemical sensor and construction method Download PDF

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CN110982879A
CN110982879A CN201911235748.9A CN201911235748A CN110982879A CN 110982879 A CN110982879 A CN 110982879A CN 201911235748 A CN201911235748 A CN 201911235748A CN 110982879 A CN110982879 A CN 110982879A
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许文菊
滑笑雨
廖羽梦
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Abstract

The invention relates to an LAMP hydrogen ion driven i-motif conversion ratio type electrochemical sensor and a construction method thereof, which combines the conventional LAMP technology and electrochemical detection, and utilizes a double dumbbell-shaped structure intermediate formed by extending short-chain DNA of a target object to carry out LAMP amplification, and a byproduct H thereof+The i-motif conformation conversion is induced to realize the obvious change and amplified output of the ratio type electrochemical signal, the complexity and the limitation of the design of the template DNA and the primer of the conventional LAMP technology are avoided, the high specificity, the simplicity, the convenience and the rapidness of LAMP are ensured, and the detection sensitivity is improved. The signal ratio of the two electrochemical probes can effectively reduce background signals, ensure high specificity, high sensitivity, good stability and regenerationAnd (4) sex. The electrochemical detection method established by the invention is simple, convenient and quick; other auxiliary reactants are not required to be introduced, so that the specificity and the sensitivity of quantitative detection are improved, the analysis time is shortened, and the detection cost is reduced.

Description

LAMP hydrogen ion driven i-motif conversion ratio type electrochemical sensor and construction method
Technical Field
The invention belongs to the technical field of biosensors, and relates to a LAMP hydrogen ion driven i-motif conversion ratio type electrochemical sensor and a construction method thereof.
Background
In recent years, some genetic diseases, malignant tumors and the like seriously threaten the life health of human beings and cause serious economic burden to society. Wherein the AIDS is caused by Human Immunodeficiency Virus (HIV). According to the statistics of the world health organization, about 3700 ten thousand people are infected with HIV in 2016, and about 70 ten thousand people are in China. Numerous studies have demonstrated a significant increase in the risk of HIV-infected people co-infecting other viruses, such as human papillomavirus. Therefore, the method can sensitively, quickly, conveniently and accurately detect HIV specific markers (such as DNA, RNA, protein and the like), and has extremely important practical significance and social value for early diagnosis, treatment, disease tracking and the like.
The amplification mechanism is that gene sequence as long as 150, even more than 200 bases is used as target template, under the action of DNA polymerase, 3'-OH at the end of primer chain initiates nucleophilic attack to α -phosphorus atom of deoxynucleotide triphosphate (dNTPs), H on 3' -OH is replaced by nucleotide base to release H+And pyrophosphate ion, the primer is continuously extended to realize 109And (4) magnification. Thus, a large amount of H is produced in addition to the main product of double-stranded DNA of varying length+(also, H is produced by hydrolysis of pyrophosphate)+) Causes the pH of the LAMP reaction solution to change (LAMP-H)+)。
The LAMP technology has high specificity, simple operation, high speed and high efficiency, does not need special expensive instruments, and is widely used for detecting bacteria, viruses, biological enzyme activity, small organic molecules and transgenic food, diagnosing clinical diseases, identifying embryo sex and the like. However, there are many disadvantages, such as too long template for amplifying the target, high requirement for primer design, poor recognition capability for single nucleotide polymorphism, and difficulty in accurate directional control of the amplified product. Common direct detection methods such as gel electrophoresis, nephelometry, colorimetry and fluorescence, and indirect pH measurement greatly limit the practical application capability of the LAMP method due to low quantitative sensitivity, poor stability, inconvenient operation and the like. By changing the LAMP reaction apparatus, e.g. in connection with microfluidics or capillariesThe use is complex, the cost of the equipment is high, the operation is complicated and time-consuming, and the technical requirement is high; and biological ligase or cutting enzyme is introduced in the LAMP reaction process, or magnetic beads form an emulsion microreactor, and then the steps of centrifugation, magnetic separation, emulsion breaking, elution and the like are carried out, so that the process is complicated and time-consuming, a new reagent is introduced, the LAMP reaction process can be changed, the uncertainty and complexity of the reaction system dynamics process are aggravated, the LAMP reaction solution is more diversified, more potential interference and false positive signals are brought to subsequent quantitative detection, and the specificity and sensitivity of the LAMP technology are reduced to a certain extent. Recently, a double dumbbell structure DNA is formed by a reverse transcription and ligation reaction of a target miRNA with only about 20-30 bases through a strand hybridization reaction to initiate LAMP reaction, and although the design of a DNA template and a primer is greatly simplified and the application range of LAMP is widened, the LAMP amplification process and the product composition are complicated by the reverse transcription and ligation reaction. Recently, LAMP-H was introduced+After dimer i-motif is induced to form, modified electrode surface is introduced to start enzyme-supported DNA walking amplification, and the electrochemical biosensor for detecting influenza virus DNA is established. The method provides a new idea and a new way for combining LAMP amplification with simple, convenient, rapid, high-sensitivity and wide-signal-window electrochemical analysis and establishing a novel DNA electrochemical biosensor. However, LAMP-H is not yet available+Report on the method of ratiometric electrochemical analysis of the converted signal.
Disclosure of Invention
In view of the above, the invention aims to provide a LAMP hydrogen ion driven i-motif conversion ratio type electrochemical sensor and a construction method thereof.
In order to achieve the purpose, the invention provides the following technical scheme:
1. a method for constructing an LAMP hydrogen ion-driven i-motif conversion ratio type electrochemical sensor comprises the steps of firstly reacting two single-stranded DNAs marked by different electroactive substances, then dropwise adding an obtained product to the surface of an electrode, and finally dropwise adding an LAMP reaction solution on the surface of the electrode to complete construction of the sensor; the LAMP reaction solution is prepared by the following method: amplification Using hDNA and two Special Stem-Loop hairpin DNA templates and precursorsAfter amplification, preparing a special double dumbbell DNA structure with an inner primer binding site, and then obtaining a large amount of by-product H by using the structure as an initial template through LAMP amplification+The LAMP reaction solution of (1). The nucleotide sequence of hDNA is shown in SEQ ID NO. 1.
hDNA: 5'-ACTGCTAGAGATTTTCCACAT-3', as shown in SEQ ID NO. 1.
Preferably, the two single-stranded DNAs (S1 and S2) are respectively marked by ferrocene Fc and methylene blue MB to obtain Fc-S1 and MB-S2, which are electrochemical signal probes. The nucleotide sequences are as follows:
S1：5’-SH-(CH2)6-AATGCAGTGGGAGGGGAAGGGAGGGGACTGCATT-3' as shown in SEQ ID NO. 6;
s2: 5'-CCCCTCCCTTCCCCTCCC-3', as shown in SEQ ID NO. 7.
Further preferably, the reaction temperature of Fc-S1 and MB-S2 is room temperature (25 ℃), the reaction time is 2 hours, and the resulting product is added dropwise to the electrode surface and incubated for 16 hours.
Further preferably, the Fc-S1 is modified with thiol (-SH) and Fc at the 5 'end and 3' end of S1, respectively, the conformation in the free state is a hairpin structure, and Fc-S1 is bound to the electrode surface through Au — S bond; the MB-S2 modified MB at the 3' end of S2, 18 bases of which are rich in 14C bases, can form an i-motif structure with pH response, and is complementary to 18 bases of the stem and loop of Fc-S1, and can open and hybridize with Fc-S1.
Preferably, the inner primers are BIP and FIP.
Further preferably, the hybridization reaction conditions are: the PCR instrument was used to perform a closed tube reaction at 50 ℃ for 20 minutes.
Further preferably, the HT is a DNA template containing a stem-loop hairpin structure designed based on the base sequence (containing 21 bases) of hDNA, and the 3' end of the DNA template is provided with a phosphate group (PO)4 3-) Modifying, namely, a complementary sequence of hDNA is arranged near the 3' end; the HP is a DNA precursor containing a stem-loop hairpin structure, and 21 bases in the 3' end direction of the HP can be hybridized with 21 bases close to a complementary sequence of the hDNA in the HT; the base sequence of the BIP is a segment B1C-B2 of HT; the base sequence of the FIP is a section of F1C-F2 of HP. Each nucleotide sequenceThe following were used:
DNA template HT: 5'-ATCGTCGTGACTGTTTGTAATAGGACAGAGCCCCGCACTTTCAGTCACGACGATTTTATG TCTGGTCTAGGGATTATG-3', as shown in SEQ ID NO. 2;
DNA precursor HP: 5 '-CGACAGCAGAGGATTTGTTGTGTGGAAGTGTGAGCGGATTTTCCTCTGCTGTCGTTTTC ATAATCCCTAGACCAGACATCACACTTATGTGGAAAATCTCTAGCAGT-phosphate-3', as shown in SEQ ID NO. 3;
the inner primer BIP: 5'-ATCGTCGTGACTGTTTGTAATAGGACAGAGCCCCGCAC-3', as shown in SEQ ID NO. 4;
inner primer FIP: 5'-CGACAGCAGAGGATTTGTTGTGTGGAAGTGTGAGCGGA-3', as shown in SEQ ID NO. 5.
Preferably, the reaction conditions for LAMP amplification are: the reaction was carried out in a PCR apparatus at 65 ℃ for 40 minutes with the tube closed.
Preferably, the specific steps are as follows:
(1) preparing a special double dumbbell DNA structure which has the BIP and FIP binding sites of the inner primers and can be extended;
(2) adding inner primers BIP and FIP, taking the double dumbbell DNA structure as an initial template, and performing rapid, simple and efficient extension and amplification to obtain a product containing a large amount of byproduct H+The LAMP reaction solution of (1);
(3) reacting the two electrochemical signal probes Fc-S1 and MB-S2 at room temperature for 2 hours, and then dropwise adding the two electrochemical signal probes Fc-S1 and MB-S2 onto the surface of a glassy carbon electrode with gold electrodeposited;
(4) and dropwise adding an LAMP reaction solution on the surface of the electrode.
Further preferably, in the step (1), the preparation method of the special double dumbbell DNA structure is as follows: the target hDNA and two special stem-loop hairpin DNA templates HT, a DNA precursor HP, DNA polymerase Bst and dNTPs react in a PCR instrument at 50 ℃ in a closed tube for 20 minutes to form a special double dumbbell DNA structure which has binding sites of the inner primers BIP and FIP and can be extended.
2. The LAMP hydrogen ion driven i-motif conversion ratio type electrochemical sensor constructed by the method is provided.
3. The sensor is applied to the quantitative detection of HIV marker DNA.
4. A LAMP hydrogen ion driven i-motif conversion ratio type quantitative detection method utilizes the sensor to measure electrochemical response signals of the two electroactive substances, thereby realizing quantitative detection of hDNA.
Preferably, the specific method is as follows: after the sensor was gently washed, the Square Wave Voltammetric (SWV) electrochemical responses of Fc and MB were measured in phosphate buffered saline (PBS, pH 7.0) and quantitative detection of hDNA was achieved by the ratio of the two current signals.
The invention has the beneficial effects that:
the invention combines the conventional LAMP amplification technology with high-sensitivity electrochemical detection, and performs LAMP amplification through a double dumbbell structure intermediate formed by extending short-chain DNA of a target object, wherein a byproduct H is generated+The i-motif conformation conversion is induced to realize the obvious change and amplified output of ratio type electrochemical signals, the complexity and the limitation of the design of template DNA and primers in the conventional LAMP technology are avoided, the design of the template and the primers is simplified, the application range of the LAMP technology is widened, the high specificity, the simplicity, the convenience and the rapidness of LAMP are ensured, the detection sensitivity is improved, and the condition that the LAMP reaction byproduct H is not utilized is compensated+Blank for ratiometric electrochemical analysis of the converted signal. The signal ratio of the two electrochemical probes can effectively reduce background signals, and ensure high specificity, high sensitivity, good stability and reproducibility. The electrochemical detection method established by the invention is simple, convenient and quick; other auxiliary reactants are not required to be introduced, the detection specificity and sensitivity are improved, the analysis time is shortened, and the detection cost is reduced. The summary is as follows:
(1) the invention combines the simple and rapid LAMP amplification with the high sensitivity of electrochemistry, performs LAMP amplification through a double dumbbell structure intermediate formed by extending the short-chain DNA of the target object, does not need complex and expensive instruments, greatly simplifies the design of DNA templates and primers, and has the advantages of high efficiency, low cost, simple steps and easy operation.
(2) The invention utilizes the ratio of signal change of two signal probes, has low background signal, high sensitivity, accuracy and specificity, good stability, reproducibility and universality, and provides a new thought and way for detecting other disease marker DNA or RNA similar to hDNA.
Drawings
In order to make the object, technical scheme and beneficial effect of the invention more clear, the invention provides the following drawings for explanation:
FIG. 1 shows hairpin structures of HT, HP and Fc-S1.
FIG. 2 is a schematic diagram of the formation (A) of a LAMP reaction double dumbbell structure template and the LAMP reaction process (B). The inset shows that white magnesium pyrophosphate precipitate of LAMP reaction proves that (+), (-) is comparison of LAMP reaction solution without hDNA participation.
FIG. 3 is a schematic diagram of the assembly process of the ratiometric hDNA electrochemical biosensor: dripping the solution after LAMP reaction initiated by hDNA on the surface of the modified electrode, LAMP-H+Inducing i-motif structural transformation, leading the MB-S2 signal probe to leave the surface of the electrode, and reducing the SWV signal; meanwhile, Fc-S1 is folded into a hairpin structure, Fc is close to the electrode surface, and the SWV signal of Fc is enhanced. The inset is a comparison of the SWV response curves of the ratiometric sensor in the absence and presence of the target hDNA.
FIG. 4 is a schematic diagram of cyclic voltammetry curves, AC impedance plots, and electrode construction process. Wherein, A and B are respectively Fe (CN) with the gradual modification process of the constructed ratio type sensor at 5mM6 3-/4-The cyclic voltammetry Curves (CV) and alternating current impedance plots (EIS) are measured in solution, and the electrodes corresponding to the curves a to e are respectively a bare Glassy Carbon Electrode (GCE), depAu/GCE, S1: S2/depAu/GCE, HT/S1: S2/depAu/GCE and LAMP-H+(ii)/HT/S1: S2/depAu/GCE; c is a schematic representation of the corresponding electrode construction process (note: the S1 and S2 unmodified Fc and MB used).
FIG. 5 shows a constructed ratio sensor in phosphate buffered saline (pH 7.0, PBS containing 10mM Na)2HPO4，10mMKH2PO4And 2mM MgCl2) The electrodes corresponding to the curves b-f are depAu/GCE, Fc-S1: MB-S2/depAu/GCE, HT/Fc-S1: MB-S2/depAu/GCE and LAMP-H respectively+MB-S2/depAu/GCE without target hDNA (blank) and with target hDNA (at a concentration of 10 pM).
FIG. 6 is a LAMP reaction gel electrophoresis, Lane M is DNA-markers (25, 50, 75, 100, 150, 200, 300, 400 and 500 bp); lane 1 target hDNA concentration 10 nM; lane 2 target hDNA concentration 1.0 pM.
Detailed Description
Preferred embodiments of the present invention will be described in detail below with reference to the accompanying drawings.
The term "room temperature" as used herein means 25 ℃.
Example (b):
(1) sequence design:
taking HIV marker DNA (hDNA) as an example, in NUPACK website (A)www.nupack.org) All base related sequences based on hDNA were designed. As shown in table 1.
TABLE 1 DNA base sequences
Figure BDA0002304830640000051
Figure BDA0002304830640000061
The hairpin structures of HT, HP and Fc-S1 are shown in FIG. 1.
(2) Formation of double dumbbell structure DNA (LAMP reaction template) (fig. 2):
in a 20. mu.L microcentrifuge tube, a total volume of 12. mu.L of various concentrations of hDNA, 0.4. mu.M HT, 0.4. mu.M MHP, 2.8mM dNTPs, 8U Bst enzyme and 20mM Tris-HCl buffer solution (pH 7.4) were contained. Tris-HCl solution containing 10mM KCl, 10mM (NH)4)2SO4，4mM MgSO4And Triton X-100 with a mass concentration of 0.1%. The uniformly mixed solution was reacted in a PCR apparatus set at 50 ℃ for 20min, and then cooled to room temperature.
(3) LAMP reaction:
to the above solution was added the prepared solution (total volume 8 μ L): contains 4. mu.M BIP, 4. mu.M FIP, and 1M betaine. After the solutions were mixed uniformly, they were reacted at 65 ℃ for 40min in a PCR instrument and then cooled to room temperature. Storing at 4 deg.C for use.
(4) Electrode modification and feasibility verification (fig. 3):
bare glassy carbon electrodes (diameter 4mm) were used separately0.3 μm and 0.05 μm Al2O3Grinding the powder, washing with secondary distilled water, and respectively performing ultrasonic treatment in anhydrous ethanol and secondary distilled water for 20 min; putting the washed glassy carbon electrode in HAuCl with the mass concentration of 1%4Carrying out electrodeposition for 30s in the solution at a constant potential of-0.2V; then dropwise adding a solution obtained after the Fc-S1 and the MB-S2 react for 2 hours at room temperature to the surface of the modified electrode, and standing for 16 hours at room temperature; then 10 mul of hexanethiol (concentration 0.1 mM, 96%, HT) is dripped for 30min, and nonspecific adsorption sites are closed; continuously dropwise adding 10 mu L of the solution after LAMP reaction, sealing and placing for 1 hour at room temperature, and storing the prepared electrode at 4 ℃ for later use.
Specifically, the following description is provided:
to verify successful modification of the electrodes, the electrodes were incubated with probe DNA without Fc and MB modification (S1 and S2) using double distilled water temperature and washing for each step, followed by a 5mM [ Fe (CN)6]3-/4-In 1.0mL of a PBS solution (pH 7.0) to determine the CV and EIS; the potential scanning range of CV is-0.2-0.6V, and the scanning speed is 100mV s-1(ii) a EIS frequency range of 10-1～105Hz, excitation signal of 5mV, apparent potential of 220 mV. (FIG. 4)
(5) Electrochemical detection and analytical performance:
after the electrode is washed mildly, square wave volt-ampere (SWV) electrochemical signals of Fc and MB are measured in 1.0mL PBS (pH 7.0) with the concentration of 1.0mL, the potential scanning range is-0.5-0.6V, and the frequency is 15 Hz; comparing the result with the SWV signal before incubation of the LAMP solution; after the LAMP reaction is carried out by measuring hDNA with different concentrations, the SWV signal of the electrode is modified, the quantitative detection of the hDNA is realized through the peak current ratio of Fc and MB, and the analysis performances such as the linear range, the lower detection limit (10 times of parallel measurement) and the like are determined. (FIG. 5)
(6) Gel electrophoresis analysis:
the LAMP reaction products of two different concentrations of hDNA were analyzed by gel electrophoresis. At room temperature, using agarose with the mass concentration of 8% and 1 xTBE buffer solution to dye by using loading buffer, adding 12 mu L of sample mixed solution, and then performing 90min at the voltage of 120V; then observed with a gel imaging system and photographed (fig. 6). Visible, with DNAmarker (Lane M, containing 25, 50, 75, 100, 150, 200, 300, 400 and 500bp) presented "ladder-like" bands (Lane 1 and Lane 2) after LAMP reaction at both concentrations of hDNA (10 nM and 1 pM); that is, when hDNA exists in the detection system, LAMP amplification can occur, and amplification products with different lengths and different molecular weights and different base numbers are generated, which shows that the LAMP amplification releases H+The feasibility of (3).
Finally, it is noted that the above-mentioned preferred embodiments illustrate rather than limit the invention, and that, although the invention has been described in detail with reference to the above-mentioned preferred embodiments, it will be understood by those skilled in the art that various changes in form and detail may be made therein without departing from the scope of the invention as defined by the appended claims.
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Claims (10)

1. A method for constructing an LAMP hydrogen ion-driven i-motif conversion ratio type electrochemical sensor is characterized in that two DNA single chains marked by different electroactive substances are reacted, then the obtained product is dripped on the surface of an electrode, and finally LAMP reaction solution is dripped on the surface of the electrode to finish the methodConstructing the sensor; the LAMP reaction solution is prepared by the following method: amplifying hDNA and two special stem-loop hairpin DNA templates and precursors to prepare a special double dumbbell DNA structure with an inner primer binding site, and performing LAMP amplification by taking the structure as an initial template to obtain a large amount of by-product H+The LAMP reaction solution of (1).
2. The construction method of claim 1, wherein the two DNA single strands are S1 and S2, which are labeled with ferrocene Fc and methylene blue MB respectively to obtain Fc-S1 and MB-S2, which are electrochemical signaling probes.
3. The method of claim 2, wherein the reaction temperature of Fc-S1 and MB-S2 is room temperature, the reaction time is 2 hours, and the resulting product is dripped onto the electrode surface and incubated for 16 hours.
4. The method of claim 1, wherein the inner primers are BIP and FIP.
5. The construction method according to claim 1, wherein the LAMP amplification reaction conditions are as follows: the reaction was closed in a PCR apparatus at 65 ℃ for 40 minutes.
6. The construction method according to claim 1, characterized by comprising the following specific steps:
(1) preparing a special double dumbbell DNA structure which has the BIP and FIP binding sites of the inner primers and can be extended;
(2) adding inner primers BIP and FIP, taking the double dumbbell DNA structure as an initial template, and performing rapid, simple and efficient extension and amplification to obtain a product containing a large amount of byproduct H+The LAMP reaction solution of (1);
(3) reacting the two electrochemical signal probes Fc-S1 and MB-S2 at room temperature for 2 hours, and then dropwise adding the two electrochemical signal probes Fc-S1 and MB-S2 onto the surface of a glassy carbon electrode with gold electrodeposited;
(4) and dropwise adding an LAMP reaction solution on the surface of the electrode.
7. The method for constructing a double dumbbell DNA structure according to claim 6, wherein the method for preparing the special double dumbbell DNA structure is as follows: the target hDNA and two special stem-loop hairpin DNA templates HT, a DNA precursor HP, DNA polymerase Bst and dNTPs react in a PCR instrument at 50 ℃ in a closed tube for 20 minutes to form a special double dumbbell DNA structure which has binding sites of the inner primers BIP and FIP and can be extended.
8. A LAMP hydrogen ion driven i-motif conversion ratio type electrochemical sensor constructed by the method of any one of claims 1 to 7.
9. Use of a sensor according to claim 8 for the quantitative detection of HIV marker DNA.
10. A LAMP hydrogen ion-driven i-motif conversion ratio type quantitative detection method, characterized in that the sensor of claim 8 is used for measuring electrochemical response signals of the two electroactive substances, thereby realizing quantitative detection of HIV marker DNA.
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