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从虎斑颈槽蛇中克隆和鉴定一种新型 P-II 类蛇毒金属蛋白酶。

Cloning and identification of a novel P-II class snake venom metalloproteinase from Gloydius halys.

机构信息

Department of Bioengineering, Zhengzhou University, Zhengzhou, Henan 450001, China.

出版信息

Appl Biochem Biotechnol. 2010 Nov;162(5):1391-402. doi: 10.1007/s12010-010-8911-6. Epub 2010 Feb 20.

Abstract

Ahpfibrase was a new snake venom metalloproteinase (SVMP) which was cloned from Gloydius halys. The cDNA sequence with 1,891 base pairs encodes an open reading frame of 477 amino acids which includes a 17 amino acid signal peptide, plus a 171 amino acid segment of zymogen-like propeptide, a metalloproteinase domain of 200 amino acids, a spacer of 16 amino acids, and a disintegrin-like peptide of 73 amino acids. The metalloproteinase domain contained a conserved signature zinc-binding motif HEXXHXXGXXH in the catalytic region and a methionine-turn CIM. To determine the activity of ahpfibrase, the coding region including both the metalloproteinase domain and disintegrin region was amplified by PCR, inserted into the pET25b(+) vector, and expressed in Escherichia coli. The recombinant protein was recovered from inclusion bodies with 8 M urea and refolding was performed by fed-batch dilution method, and purified recombinant ahpfibrase showed the fibrinolytic activity and platelet aggregation-inhibition ability.

摘要

阿朴纤维酶是一种从虎斑颈槽蛇(Gloydius halys)中克隆得到的新型蛇毒金属蛋白酶(SVMP)。cDNA 序列全长 1891 个碱基对,编码一个 477 个氨基酸的开放阅读框,包括 17 个氨基酸的信号肽,171 个氨基酸的酶原样前肽段,200 个氨基酸的金属蛋白酶结构域,16 个氨基酸的间隔区和 73 个氨基酸的整联蛋白样肽。金属蛋白酶结构域在催化区域包含一个保守的锌结合基序 HEXXHXXGXXH 和一个蛋氨酸-turn CIM。为了确定阿朴纤维酶的活性,通过 PCR 扩增包括金属蛋白酶结构域和整联蛋白结构域的编码区,将其插入 pET25b(+)载体,并在大肠杆菌中表达。重组蛋白从包涵体中用 8 M 尿素回收,通过分批补料稀释法进行复性,纯化的重组阿朴纤维酶显示出纤维蛋白溶解活性和血小板聚集抑制能力。

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