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

A kind of recombinant protein and its construction method and application

A recombinant protein and fibronectin technology, applied in the field of recombinant proteins, can solve the problems of poor transdermal performance of protein-polypeptide complexes, poor stability of fibronectin, limited application of protein and polypeptides, etc. Low cost, simple preparation and low effect

Active Publication Date: 2021-12-17
MEIMU (BEIJING) TECH CO LTD
View PDF10 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0006] In the prior art, the above-mentioned small molecule polypeptide and fibronectin are generally compounded by physical mixing method in the cosmetic formula. The stability of fibronectin itself is not good, and the small molecule polypeptide is added again, and the challenge of stable performance is even greater, and the preparation cost also higher
At the same time, because there is a physical barrier on the surface of the skin, most of the macromolecular active ingredients are prevented from acting through the skin, because the transdermal performance of the protein-peptide complex is often poor, so that the originally highly active polypeptide cannot fully exert its due effect. effect, which further limits the application of protein peptides in cosmetics

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
  • A kind of recombinant protein and its construction method and application
  • A kind of recombinant protein and its construction method and application
  • A kind of recombinant protein and its construction method and application

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0039] The research and development of embodiment 1 transdermal fibronectin mutant

[0040] 1. Mutant research and development ideas:

[0041] There are surfactants, thickeners, essences, polyols and other ingredients in cosmetic formulations, which will affect the stability of protein peptides in cosmetics. At the same time, cosmetics may encounter high temperature conditions during transportation and storage, which will accelerate the degradation of protein peptides.

[0042] In the present invention, after recombining the transdermal peptide and fibronectin, according to the three-dimensional structural characteristics of the recombinant protein, the sequence of the transdermal peptide fibronectin is shown in SEQ ID No. The stability of the mutation point selection effectively avoids the active site, and does not have any impact on the function of the recombinant fibronectin.

[0043] Experimental Design: Download the crystal structure file 1fnf.pdb of human fibronectin f...

Embodiment 2

[0049] Example 2 Construction of Transdermal Fibronectin Mutant Recombinant Protein Particles

[0050] In the embodiment of the present invention, the amino acid sequence of the recombinant transdermal fibronectin mutant (A-5) is shown in SEQ ID No.1, wherein ACSPPHSKSHC is a transdermal peptide sequence, which can enhance the transdermal absorption performance of the protein, GGGGS For the link between the transdermal peptide and fibronectin.

[0051] Build method:

[0052] (1) According to the position design of the relevant sequence of the commercial vector pPICZaA, the enzyme cutting sites EcoR I and SalI were selected; the DNA sequence encoding the transdermal fibronectin mutant recombinant protein is shown as SEQ ID No.2;

[0053] (2) There is a restriction endonuclease site at the 5' and 3' ends of the synthetic recombinant protein DNA sequence, corresponding to EcoR I and SalI respectively;

[0054] (3) Insert the target fragment of the recombinant protein into the r...

Embodiment 3

[0055] Example 3 Construction of Transdermal Fibronectin Mutant-Collagenase Inhibiting Peptide Recombinant Protein Particles

[0056] In the embodiment of the present invention, the transdermal fibronectin mutant-collagenase inhibitory peptide recombinant protein is the flexible end of the recombinant transdermal fibronectin mutant prepared in Example 2, which is connected to the collagenase inhibitory peptide through a connecting peptide. The amino acid sequence is shown in SEQ ID No.4.

[0057] Build method:

[0058] (1) According to the position design of the relevant sequence of the commercial vector pPICZaA, the enzyme cleavage sites EcoR I and SalI were selected; the DNA sequence encoding the transdermal peptide-fibronectin mutant-collagenase inhibitory peptide recombinant protein is shown in SEQ ID No.5;

[0059] (2) There is a restriction endonuclease site at the 5' and 3' ends of the synthetic recombinant protein DNA sequence, corresponding to EcoR I and SalI respect...

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 mutant of recombinant transdermal fibronectin, which consists of transdermal fibronectin connected by connecting peptides to form recombinant transdermal fibronectin, and then the E174D and P292G positions of the amino acid sequence of the recombinant transdermal fibronectin are modified. The amino acid sequence of the recombinant transdermal fibronectin mutant is shown in SEQ ID No.1. The recombinant protein provided by the invention has better stability and guaranteed efficacy, is easy to prepare and has low cost, and greatly expands the application of fibronectin and collagenase inhibitory peptides in cosmetics.

Description

technical field [0001] The invention relates to a recombinant protein, in particular to a highly stable recombinant protein used for cosmetic preparation or addition and its construction method. Background technique [0002] Fibronectin (also known as Fn) is a high molecular weight glycoprotein in the extracellular matrix. FN is produced by liver and vascular endothelial cells and widely exists in animal tissues and interstitial fluids. It is a macromolecular glycoprotein with the biological function of cell regeneration and repair. It has been used in clinical medicine, including the treatment of spinal cord. Sickness, burns, etc. Experience has proved that fibronectin has a repairing effect on sensitive skin, red blood streaks, acne, sun damage and other skin problems. [0003] Although fibronectin has excellent skin care effects, its thermal stability and chemical stability are not good. Poor thermal stability is mainly reflected in the precipitation, precipitation or ...

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 Patents(China)
IPC IPC(8): C07K19/00C12N15/62C12N15/81A61K8/64A61Q19/00A61Q19/08A61P17/10
CPCC07K14/78C07K14/811C12N15/815A61K8/64A61Q19/004A61Q19/005A61Q19/08A61P17/10C07K2319/00
Inventor 王娟刘廷竹
Owner MEIMU (BEIJING) TECH CO LTD
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

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com