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含RGD三肽的蜘蛛拖牵丝蛋白聚合物的生物合成与纯化

[Biological synthesis and purification of spider dragline silk protein polymers containing RGD three peptide].

作者信息

Li Min, Huang Jiankun, Tu Guiyun, Huang Xi

机构信息

College of Bioengineering, Fujian Normal University, Fuzhou 350007, China.

出版信息

Sheng Wu Yi Xue Gong Cheng Xue Za Zhi. 2004 Dec;21(6):1006-10.

Abstract

Spider dragline silk is one of most perfect fibrous proteins in nature. As biomaterials, it has a wide application in tissue engineering due to its unique mechanical properties, good biocompatibility, slow degradation. In this paper, based on the highly repetitive sequence of spider dragline silk and with the introduced RGD peptide codons which involve cell adhesion, the DNA monomer sequence encoding RGD-spider dragline silk was synthesized, and then was used to construct the multimers by the strategy of "head to tail"; the multimers were ligated into prokaryotic expression vector pET-30a, and then the B121 (DE3) pLyS, were transformed the expression of recombinant protein was induced by the addition of IPTG. SDS-PAGE analysis shows that the molecular weight of products expressed here are 35KD and 60KD respectively in agreement with the desired. Western assay was used for determining the specification of products. Further, the purification process was groped for the producing of large quantity of synthetic proteins through high density fermentation.

摘要

蜘蛛拖牵丝是自然界中最完美的纤维蛋白之一。作为生物材料,由于其独特的机械性能、良好的生物相容性和缓慢的降解性,它在组织工程中有着广泛的应用。本文基于蜘蛛拖牵丝的高度重复序列,并引入了涉及细胞黏附的RGD肽密码子,合成了编码RGD-蜘蛛拖牵丝的DNA单体序列,然后采用“头对尾”策略构建多聚体;将多聚体连接到原核表达载体pET-30a中,再转化B121(DE3)pLyS,通过添加IPTG诱导重组蛋白表达。SDS-PAGE分析表明,此处表达产物的分子量分别为35KD和60KD,与预期相符。采用Western检测法确定产物的规格。此外,通过高密度发酵摸索了大量合成蛋白的纯化工艺。

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