Construction, fermentation and purification of high polymer spider dragline silk protein containing RGD peptide.
- Author:
Chao-Ran RUAN
1
;
Jing-Xing HUANG
;
Mei-Hong WEI
;
Min LI
Author Information
1. College of Life Sciences, Fujian Normal University, Fuzhou 350108, China.
- Publication Type:Journal Article
- MeSH:
Animals;
Escherichia coli;
genetics;
metabolism;
Fermentation;
Fibroins;
biosynthesis;
genetics;
Molecular Sequence Data;
Oligopeptides;
biosynthesis;
chemistry;
genetics;
Polymers;
metabolism;
Protein Engineering;
Recombinant Proteins;
biosynthesis;
genetics;
isolation & purification;
Transformation, Bacterial
- From:
Chinese Journal of Biotechnology
2007;23(5):858-861
- CountryChina
- Language:Chinese
-
Abstract:
Spider silk is a natural protein fibroin with excellent character as it is light and tenacious. It has a wild potential applications in the biomedical field due to its good biocompatibility and degradation. Arginine-glycine-aspartic acid (RGD) is a highly conserved amino acid sequence of many adhesion protein. Biological materials binding with RGD peptide in the surface can promote cells adhesion, migration and proliferation. Our lab had constructed the 16 muhimers with the introduced RGD peptide codons which involve cell adhesion for the first time. It was found that the mechanical capability of the 16 mulimer protein was very limited because of the big gap in molecular weight with nature spider proteins when it was used to made biomaterial scaffold.In this paper,based on the 16 multimers of the highly, repetitive sequence of spider dragline silk and with RGD peptide condons which has been constructed by our lab forestall, it was used to construct the 32 and 64 multimers sequence of spider dragline silk by the strategy of "head to tail". The 32 and 64 multimers were ligated into prokaryotic expression vector pET-30a, and then the B121 (DE3) pLysS. The fragments were in agreement with the desired through digestion, agarose gel electrophoresis respectively. By registration into the GenBank data-base, the serial numbers of DQ469929 and DQ837297 were gained respectively. The expression of recombinant protein was introduced by the addition of IPTG. SDS-PAGE analysis shows that the molecular weight of products expressed here are 102 kD and 196.6kD in agreement with the desired respectively. It was the first time for the high polymer spider dragline silk protein expressed in prokaryotic biology. Furthermore, a larger quantity of synthetical proteins with high density fermentation were searched after, and a suit of high efficient purification methods for 32 multimers protein were established.
