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

High molecular weight recombinant silk or silk-like protein, and micro- or nanoscale spider-web fiber or spider-web-like fiber produced using the recombinant silk or silk-like protein

A spider silk fiber, high molecular weight technology, applied in the direction of single-component fibroin artificial filament, single-component protein rayon, fiber chemical characteristics, etc., can solve problems such as protein inhomogeneity

Active Publication Date: 2013-01-30
MEDICOSBIOTECH INC
View PDF2 Cites 18 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

There is no report on dragline protein with higher molecular weight, and the reason is believed to be that there are problems such as inhomogeneity caused by errors in the protein synthesis process

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
  • High molecular weight recombinant silk or silk-like protein, and micro- or nanoscale spider-web fiber or spider-web-like fiber produced using the recombinant silk or silk-like protein
  • High molecular weight recombinant silk or silk-like protein, and micro- or nanoscale spider-web fiber or spider-web-like fiber produced using the recombinant silk or silk-like protein
  • High molecular weight recombinant silk or silk-like protein, and micro- or nanoscale spider-web fiber or spider-web-like fiber produced using the recombinant silk or silk-like protein

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0066]Example 1: Construction of high molecular weight silk protein expression vectors pSH32, pSH48, pSH64, pSH80 and pSH96, construction of nucleic acid sequence expression vectors encoding glycine tRNA, and preparation of recombinant silk proteins with various molecular weights.

[0067] 1-1: Construction of pSH32, pSH48, pSH64, pSH80 and pSH96.

[0068] All genetic manipulation steps were performed according to standard methods (Sambrook et al., Molecular cloning: a laboratory manual, 2nd Ed., Cold Spring Harbor Laboratory Press, Cold Spring Harbor, New York, 1989). In order to construct recombinant plasmid pSH32, plasmid pSH16a (Lee et al., Theories and Applications of Chem.Eng., 8(2): 3969, 2002) (sequence number: 13) was treated with restriction enzymes SpeI and NheI (New England Biolabs, USA) digested to obtain a 1.7kb fragment, which was treated with the restriction enzyme SpeI and connected to the dephosphorylated plasmid pSH16a, thereby obtaining the nucleic acid con...

Embodiment 2

[0087] Example 2: Production of spider silk fibers by wet spinning - the influence of molecular weight on the mechanical properties of wet spinning fibers

[0088]After dissolving the recombinant silk protein prepared in Example 1-2 in the textile solvent hexafluoroisopropanol (HFIP; Sigma) to prepare the spinning solution, use a pump (KDS100; KD Scientific) at a speed of 1-2ml / hr Injection molding of spinning solution. As for the concentration of silk protein in the spinning solution, due to the relationship between solubility and viscosity, the maximum operating concentration of natural 96-mer protein is 20% (w / v), therefore, all textiles are at the concentration of silk protein in the spinning solution It is carried out under the condition of 20% (w / v). At this time, injection molding was performed by injecting the dope solution from a 1-ml Kovax syringe through a 26-G syringe needle (KoreaVaccine Co., Ltd.) into a coagulation apparatus filled with water containing 90% (v / ...

Embodiment 3

[0093] Embodiment 3: the influence of doping solution concentration on wet-spun fiber properties

[0094] In order to examine the effect of the concentration of recombinant silk protein in the spinning solution on the properties of the spun fibers, the 16-mer, 32-mer and 64-mer proteins were spun at the maximum operating concentration, and compared with Example 2.

[0095] As a result, such as Figure 5 As shown, when the concentration of 16-mer protein increased from 20% to the highest concentration of 30%, the properties of the spun fibers were significantly improved. However, when the concentration of 32-mer protein was increased from 20% to the highest concentration of 27%, the breaking strain and tensile strength of the fibers increased, but not statistically. In addition, the maximum operating concentration of 64-mer protein was 23%, and the mechanical properties at this time were not much different from those at the concentration of 20% already tested, that is, the mec...

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

PropertyMeasurementUnit
molecular weightaaaaaaaaaa
tensile strengthaaaaaaaaaa
molecular weightaaaaaaaaaa
Login to View More

Abstract

The present invention relates to high molecular weight recombinant silk or silk-like protein, which has a molecular weight that is almost equivalent to that of natural silk protein, and to micro- or nanoscale spider-web fiber or spider-web-like fiber having improved physical properties produced using the recombinant silk of the silk-like protein. The recombinant silk or the silk-like protein according to the present invention is advantageous in that it has a high molecular weight like the dragline silk protein produced by a spider, and exhibits physical properties similar or superior to the natural silk protein when produced into fiber.; Therefore, the recombinant silk or the silk-like protein, and the spider-web fiber or spider-web-like fiber produced using the recombinant silk or silk-like protein according to the present invention can be significantly valuably used in a variety of industrial fields, such as the biotechnological fields and / or medicinal fields to which spider-web fibers are applicable.

Description

technical field [0001] The present invention relates to high molecular weight recombinant silk or silk-like proteins having a molecular weight substantially similar to natural silk proteins, and micron or nanoscale spider silk or spider silk-like fibers produced using them with improved physical properties. Background technique [0002] Spider silks, used by spiders as lifelines and in forming radial webs, are strong and elastic. When calculated per unit mass, spider silk is 5 times stronger than steel and 3 times tougher than artificial fiber Kevlar (Gosline, J.M. et al., J. Exp. Biol., 202:3295, 1999; Vollrath, F. & Knight , D.P., Nature 410:541, 2001). Therefore, as a material suitable for various industrial applications, spider drag silk has received extensive attention. In addition, spider silk is biocompatible and biodegradable, so it is expected to be applied in many biomedical fields. Unfortunately, due to the highly territorial and aggressive nature of spiders, n...

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): C07K14/435C12N15/12C12N15/63D01F4/00
CPCD01D5/0007C07K14/43518D01D5/06D01F4/02
Inventor 李相烨夏小霞钱志刚李政旭朴泳焕
Owner MEDICOSBIOTECH INC
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