Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Nucleic acid aptamer capable of identifying HCV E1E2 (hepatitis C virus E1E2), nucleic acid aptamer derivatives and screening method and application thereof

A nucleic acid aptamer and E1E2 technology, applied in the field of genetic engineering, can solve the problems of patients interrupting treatment, large side effects of combination therapy, and expensive treatment, and achieve the effect of high cost, good affinity, and specific inhibition of HCV infection

Inactive Publication Date: 2011-11-02
HUNAN UNIV
View PDF5 Cites 14 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Although the addition of ribavirin can enhance the level of sustained antiviral response, it is also associated with serious side effects (such as hemolytic anemia), which often lead to discontinuation of treatment in 20% of patients
Due to the great sequence diversity of the HCV genome, combined with the side effects of combination therapy and the high cost of treatment, it is urgent to develop new methods to effectively treat liver disease patients infected with different HCV genotypes

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Nucleic acid aptamer capable of identifying HCV E1E2 (hepatitis C virus E1E2), nucleic acid aptamer derivatives and screening method and application thereof
  • Nucleic acid aptamer capable of identifying HCV E1E2 (hepatitis C virus E1E2), nucleic acid aptamer derivatives and screening method and application thereof
  • Nucleic acid aptamer capable of identifying HCV E1E2 (hepatitis C virus E1E2), nucleic acid aptamer derivatives and screening method and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment

[0051] Example: nucleic acid aptamers capable of recognizing HCV E1E2 protein, derivatives of nucleic acid aptamers, screening methods and applications thereof.

[0052] 1. Preparation of related proteins.

[0053] 11 Preparation of HCV envelope protein E1E2 (target protein) with histidine tag.

[0054] 1.1.1 Amplification of the gene encoding HCV envelope protein E1E2

[0055] Using the pJFH1 plasmid as a template for PCR amplification, the E1E2 gene was amplified by PCR with the first primers consisting of the following primers 1 and 2 (PCR reagents were purchased from Roche, and 100 microliters of PCR tubes were purchased from Eppendorf):

[0056] Primer 1 (upstream primer):

[0057] 5'-CGCGCGAATTCGCCCAGGTGAAGAATACCAGTAGCAGCTAC-3';

[0058] Primer 2 (downstream primer):

[0059] 5'-CTGCAGAAGCTTTGCTTCGGCCTGGCCCAACA-3';

[0060] The 5' ends of the upstream and downstream primers were respectively introduced with EcoR1 restriction site and HindIII restriction site;

[00...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

The invention discloses a nucleic acid aptamer capable of identifying HCV E1E2 (hepatitis C virus E1E2), which is a DNA fragment having a sequence shown in any one of SEQ ID No.1 to SEQ ID No.5. Derivatives of the nucleic acid aptamer include nucleotide-substituted RNA nucleic acid aptamers, skeleton-modified derivatives, peptide nucleic acid derivatives and derivatives of nucleic acid aptamer conjugated with radioactive molecules. A method for screening the nucleic acid aptamer comprises the following steps: firstly preparing HCV E1E2 proteins with histidine tags and then preparing pET200 / D / LacZ proteins with histidine tags, then immobilizing the proteins and designing a random nucleic acid library, and finally screening nucleic acid aptamers. Specifically, the screening step comprises the following steps: pre-treating the DNA library, performing reverse screening, performing forward screening, and repeatedly screening, to obtain the nucleic acid aptamer with strong competitiveness and optimized sequence length. The nucleic acid aptamer and derivatives thereof can be applied to preparing HCV E1E2 protein detection kits or diagnostic kits as well as agents for suppressing HCV infection in liver cells.

Description

technical field [0001] The invention belongs to the technical field of genetic engineering, and in particular relates to a nucleic acid aptamer, a derivative of the nucleic acid aptamer and a screening method and application thereof. Background technique [0002] Hepatitis C virus (HCV) infection is a serious global health problem, with 200 million infected people worldwide. It is estimated that there are 3-4 million new infections each year. About 40 million to 50 million people in my country are infected with HCV, second only to the number of hepatitis B carriers. [0003] Currently, the standard treatment for hepatitis C virus is interferon or interferon combined with ribavirin. Treatment of patients infected with genotypes 2 and 3 has an HCV eradication rate of 75% to 90%, however, about 50% of patients infected with HCV types 1 and 4 remain insensitive. Although the addition of ribavirin can enhance the level of sustained antiviral response, it can also bring about s...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Applications(China)
IPC IPC(8): C12N15/115C12N15/10C12Q1/70C12Q1/68G01N33/68A61K48/00A61P31/14C12R1/93
Inventor 朱海珍方晓红刘斌徐丽杨大荣龙樱雷少华
Owner HUNAN UNIV
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products