Cloning, direct expression, and purification of a snake venom cardiotoxin in Escherichia coli

被引:38
作者
Kumar, TKS
Yang, PW
Lin, SH
Wu, CY
Lei, B
Lo, SJ
Tu, SC
Yu, C
机构
[1] NATL TSING HUA UNIV, DEPT CHEM, HSINCHU, TAIWAN
[2] NATL YANG MING MED UNIV, INST MICROBIOL & IMMUNOL, TAIPEI, TAIWAN
[3] UNIV HOUSTON, DEPT BIOCHEM & BIOPHYS SCI, HOUSTON, TX 77204 USA
关键词
D O I
10.1006/bbrc.1996.0254
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The cardiotoxin analogue III (CTX III), isolated from the Taiwan cobra (Naja naja atra) venom, is a sixty-amino acid, all beta-sheet protein. We report the direct expression of CTX III from its synthetic gene as inclusion bodies in Escherichia coli. The yield of the expressed protein is about 40 mg/liter of the culture. CTX III trapped as inclusion bodies is dissolved and refolded by the slow refolding technique. The refolded protein is purified by reverse phase high performance liquid chromatography. The purified and refolded CTX III sample is further characterized by SDS-PAGE, circular dichroism, two-dimensional NMR spectroscopy and haemolytic activity. To our knowledge, this is the first report of the direct expression and purification of snake venom cardiotoxins. (C) 1996 Academic Press, Inc.
引用
收藏
页码:450 / 456
页数:7
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