Eureka AIR delivers breakthrough ideas for toughest innovation challenges, trusted by R&D personnel around the world.

Mutant IRS-1 PTB domain proteins, and coding sequence and application thereof

A domain protein, IRS-1 technology, applied in the application field of PTB-MUTANT fusion gene and its prokaryotic expression vector, can solve the problems of high price, large molecular weight, drug resistance, etc., to improve affinity and reduce binding free energy. , the effect of enhancing affinity

Active Publication Date: 2019-04-16
HUAZHONG UNIV OF SCI & TECH
View PDF1 Cites 2 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the preparation cost of monoclonal antibody is high, the price is expensive, the quality of different batches is unstable, and the molecular weight is large, and the cell penetration ability is poor; kinase inhibitors strongly inhibit the signaling pathways related to pY in cells, and there are certain side effects. A condition in which a genetic mutation leads to drug resistance, thereby losing efficacy of the treatment 2

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
  • Mutant IRS-1 PTB domain proteins, and coding sequence and application thereof
  • Mutant IRS-1 PTB domain proteins, and coding sequence and application thereof
  • Mutant IRS-1 PTB domain proteins, and coding sequence and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0047] 1. Construction of pGEX-4T2-PTB fusion gene expression vector

[0048] 1.1 Cloning of PTB and PTB-MUTANT domain genes

[0049] According to the PTB nucleotide sequence of IRS-1 in Genbank, such as image 3 As shown, the amplification primers are designed, and considering that the vector construction is a molecular cloning method using homologous recombination, appropriate homology arms should be added when designing the primers, which are F1 and R1 respectively. The specific primer sequences are as follows:

[0050] Forward primer F1: GATCTGGTTCCGCGTttcaaagaggtctggcaag34;

[0051] Reverse primer R1: GTCAGTCAGTCACGAgaactcatcactcatggcc34;

[0052] Using the cDNA of MCF7 cells as a template, using F and R as amplification primers respectively, the PTB domain gene was amplified by PCR. The PCR system was 2x PCR Mix 10ul, F1 1ul, R1 1ul, H 2 O 6ul, cDNA 2ul. The PCR program was 98°C for 2min, 98°C for 30s, 55°C for 30s, 72°C for 30s, and 35cycle.

[0053] The primer sequ...

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

Amino acid residues of PTB domain wild-type proteins of IRS-1 are subjected to site-directed mutation, R at a 99th site is mutated to L, S at a 102nd site is mutated to A, a mutant vector is constructed, proteins are expressed and purified, and a PTB fusion protein mutant GST-PTB-R99L / S102A of IRS-1 is expressed in escherichia coli, and the affinity of the mutant specifically binding to tyrosine residue phosphorylated IGF-1R is greatly enhanced. The constructed recombinant plasmid-expressed fusion protein (Arg)9-GST-PTB-MUTANT of the PTB fusion protein mutant of IRS-1 and a cell penetrating peptide (Arg)9 can penetrate and enter cancer cells, replaces an endogenous IRS-1 protein in cancer cells to bind to IGF-1R, blocks multiple signal pathways involved in the endogenous IRS-1 protein, caninhibit the proliferation and invasion of tumor cells, and has significant anti-tumor effect.

Description

technical field [0001] The invention belongs to the field of biotechnology, relates to a protein polypeptide with strong affinity for the phosphorylated tyrosine residue of insulin-like growth factor receptor IGF-1R, relates to gene recombination, bioinformatics prediction, mutant construction and prokaryotic carrier fusion protein expression and purification, especially the application of a PTB-MUTANT fusion gene and its prokaryotic expression vector. Background technique [0002] Overview of phosphorylated tyrosine and its anti-tumor application: anti-tumor drugs mainly include cytotoxic anti-tumor drugs, anti-tumor drugs targeting cell signal transduction molecules, etc. Among them, tyrosine kinase inhibitors can penetrate cell membranes and target To tumor cells has become a hotspot in international new drug research. Phosphorylation modification of protein tyrosine is the basic mechanism to regulate cell signal transduction, and cancerous cells often show abnormally in...

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): C07K14/47C07K19/00C12N15/12C12N15/70A61K38/17A61P35/00
CPCA61K38/00C07K14/47C07K2319/10C07K2319/23C12N15/62C12N15/70
Inventor 曹轩刘安冬余悦琪邓婕罗丹妮
Owner HUAZHONG UNIV OF SCI & TECH
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Eureka Blog
Learn More
PatSnap group products