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[多环扁尾海蛇α-银环蛇毒素基因的分子克隆与表达]

[Molecular cloning and expression of an isotoxin gene, alpha-bungarotoxin, from Bungarus multicinctus].

作者信息

Wang Fang, Wang Yi-Quan

机构信息

School of Life Sciences, Xiamen University, Xiamen 361005, China.

出版信息

Yi Chuan Xue Bao. 2005 Jul;32(7):682-8.

Abstract

Abstract: Snake venom contains a number of small proteins,enzymes and other components,which displays a broad spectrum of biological activities. With the ability of specifically binding on acetylcholine acceptor, alpha-bungarotoxins are not only useful molecular probes in investigating the mechanism of neural signal transmission, but also potential pharmic preparations for neural disease treatment. In current research,cDNAs of Bungarus multicinutus venom gland were synthesized using SMART cDNA amplification kit and then, alpha-bungarotoxin genes were cloned and sequenced. Total of 20 clones were sequenced representing 14 isotoxin mRNAs of alpha-bungarotoxins. Among those clones, a novel isotoxin gene was subcloned into two expression plasmids, alpha-BgTX/pQE30a and alpha-BgTX/pGEX-4T-1, and transformed into E. coli. After inducing with IPTG, fused protein of GST-alpha-BgTX was successfully expressed at level of 30% gross proteins of bacteria. More than 25% of fused protein was in the soluble fraction and the rest in inclusion body.

摘要

摘要

蛇毒含有多种小蛋白质、酶及其他成分,具有广泛的生物活性。α-银环蛇毒素能够特异性结合乙酰胆碱受体,不仅是研究神经信号传递机制的有用分子探针,也是治疗神经疾病的潜在药物制剂。在当前研究中,使用SMART cDNA扩增试剂盒合成了多环眼镜蛇毒腺的cDNA,随后克隆并测序了α-银环蛇毒素基因。共对20个克隆进行了测序,代表了14种α-银环蛇毒素的同毒素mRNA。在这些克隆中,一个新的同毒素基因被亚克隆到两个表达质粒α-BgTX/pQE30a和α-BgTX/pGEX-4T-1中,并转化到大肠杆菌中。用异丙基-β-D-硫代半乳糖苷(IPTG)诱导后,GST-α-BgTX融合蛋白成功表达,表达量占细菌总蛋白的30%。超过25%的融合蛋白处于可溶部分,其余在包涵体中。

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