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Nucleic acid aptamer of protein tyrosine phosphatase SHP2 and preparation method thereof

A technology of tyrosine phosphatase and nucleic acid aptamer, which is applied in the field of nucleic acid, can solve the problems that it is difficult to become a drug with therapeutic value, the cell permeability and bioavailability selectivity are not very ideal, and the compound is easy to ionize, etc., to achieve screening The effect of simple and fast detection, easy synthesis and labeling, and small molecular weight

Inactive Publication Date: 2011-06-01
XIAMEN UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

At present, although some protein tyrosine phosphatase inhibitors that perform well at the in vitro level have been found, most small molecule protein tyrosine phosphatase inhibitors are easily ionized due to their compounds, cell permeability and bioavailability And the selectivity is not very ideal, so it is difficult to become a drug of therapeutic value

Method used

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  • Nucleic acid aptamer of protein tyrosine phosphatase SHP2 and preparation method thereof
  • Nucleic acid aptamer of protein tyrosine phosphatase SHP2 and preparation method thereof
  • Nucleic acid aptamer of protein tyrosine phosphatase SHP2 and preparation method thereof

Examples

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Effect test

Embodiment 1

[0039] Example 1 In vitro screening of nucleic acid aptamers specifically binding to protein tyrosine phosphatase SHP2

[0040] 1) Dissolve the synthesized 5nmol single-stranded DNA nucleic acid library in binding buffer (12mmol / L PBS, 0.55mmol / LMgCl 2 ), conduct heat treatment: heat at 95°C for 5 minutes, place on ice for 10 minutes, and then place at room temperature for 10 minutes;

[0041] 2) Incubate the processed single-stranded DNA nucleic acid library with GST microbeads, and collect the liquid that is not bound to the GST microbeads;

[0042] 3) Incubate the liquid not bound to the GST microbeads with the SHP2-GST microbeads at 37°C for 40min;

[0043] 4) washing the incubated SHP2-GST microbeads with a binding buffer, and performing a PCR reaction on the SHP2-GST microbeads bound to the oligonucleotide;

[0044] The PCR reaction program was: pre-denaturation at 94°C for 3min, 30s at 94°C, 30s at 53°C, 30s at 68°C, 10 cycles of amplification, and final extension at ...

Embodiment 2

[0049] Example 2 Detection of the binding ability of the resulting single-stranded DNA to the protein tyrosine phosphatase SHP2 by flow cytometry

[0050] First PCR amplifies fluorescently labeled single-stranded DNA, using primer 2: 5′-Biotin-CTGACC ACGAGC TCCATT AG-3′ and primer 3: 5′-FAM-AGC GTC GAA TAC CAC TAC AG-3′, the PCR product For double-stranded DNA with FAM at the 5' end and biotin at the 3' end, add streptavidin microbeads, react for 30 minutes, then use 0.1mol / L NaOH to single-stranded, and purify through a desalting column to obtain FAM-labeled single-stranded DNA for flow cytometry analysis.

[0051] Use 0nmol / L, 5nmol / L, 10nmol / L, 20nmol / L, 50nmol / L, 100nmol / L, 200nmol / L single-stranded DNA and target protein SHP2-GST beads to determine the dissociation constant (Kd) . Use 200 μl of binding buffer to prepare DNA solutions of the above concentrations, heat at 95°C for 5 minutes, place on ice for 10 minutes, and then place at room temperature for 10 minutes. ...

Embodiment 3

[0053] Example 3 Determination of the obtained nucleic acid aptamer HJ24 by circular dichroism to form a parallel G tetramer structure

[0054] Prepare 1 μmol / L nucleic acid aptamer HJ24 solution with binding buffer, and perform heat treatment: heat at 95°C for 5 minutes, place on ice for 10 minutes, and then place at room temperature for 10 minutes. Then use the circular dichroism spectrometer to scan the CD spectrum from 400nm to 200nm with a step length of 0.1nm, repeat the scan 8 times, and the results form a negative peak and a positive peak at 240nm and 260nm respectively. This peak type is consistent with the literature (10, Sattanathan Paramasivan, Iulian Rujan, Philip H.Bolton. Circular dichroism of quadruplex DNAs: Applications to structure, cation effects and ligand binding, 2007, 43: 324-331.) The characteristic peaks of parallel G tetramers reported in coincidence, so it can be judged The obtained nucleic acid aptamer HJ24 has a parallel G tetramer structure (see ...

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Abstract

The invention discloses a nucleic acid aptamer of protein tyrosine phosphatase SHP2 and a preparation method thereof, in particular relates to a nucleic acid and provides a nucleic acid aptamer of protein tyrosine phosphatase SHP2 with high specificity and high appetency and a preparation method and application thereof. The nucleic acid aptamer of the protein tyrosine phosphatase SHP2 has a parallel tetramer structure. The preparation method comprises the following steps: designing and synthesizing a single-chain DNA (deoxyribonucleic acid) random oligonucleotide library, screening a target oligonucleotide sequence, and identifying specificity and appetency of the target oligonucleotide sequence combined with target protein by a flow analysis method. The nucleic acid aptamer obtained by screening has the advantages of no toxicity, small molecular weight and good penetrability, can be synthesized and marked easily, only specifically recognizes SHP2 protein, does not have a recognition function on other homologous protein, and can be prepared into a potential inhibitor for selectively controlling the activity of the protein tyrosine phosphatase SHP2.

Description

technical field [0001] The invention relates to a nucleic acid, in particular to a nucleic acid aptamer of protein tyrosine phosphatase SHP2 and a preparation method thereof. Background technique [0002] Protein tyrosine phosphatase SHP2 (Src homology 2 domain containing protein tyrosine phosphatase-2) is a member of the protein tyrosine phosphatase superfamily, widely distributed in the cytosol, and encoded by the PTPN11 gene in humans. Its molecular structure includes: two SH2 domains at the N-terminus, a catalytic PTP domain in the middle, a proline-rich residue at the C-terminus, and a tail structure with two tyrosine phosphorylation sites (1 , Lai LA, Zhao C, Zhang EE, et al. The Shp-2 tyrosine phosphatase. In: Arino J, Alexander D, eds. Protein Phosphatases. Berlin, Heidelberg, Germany: Springer-Verlag; 2004: 275-299; 2 , Neel BG, Gu H, Pao L. The'Shp'ing news: SH2 domain-containing tyrosine phosphatases in cell signaling. Trends Biochem Sci, 2003, 28(6):284-293). ...

Claims

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Application Information

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IPC IPC(8): C12N15/115
Inventor 杨朝勇胡佳邬杰李聪朱玲吕忠显庄峙厦
Owner XIAMEN UNIV
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