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人FKBP52的基因克隆、表达及活性研究
引用本文:裴武红,贺永怀,陈兴,李松,沈倍奋.人FKBP52的基因克隆、表达及活性研究[J].生物化学与生物物理进展,2001,28(2):236-239.
作者姓名:裴武红  贺永怀  陈兴  李松  沈倍奋
作者单位:1. 北京基础医学研究所,北京 100850
2. 北京毒物药物研究所,北京 100850
基金项目:国家“973”创新药物基金资助项目(G1998051107).
摘    要:为获得具有生物学活性的hFKBP52,来筛选新型的促神经再生药物.采用半巢式、桥联PCR及亲和层析方法,从人胎脑cDNA文库中成功扩增出hFKBP52基因,在pET28a(+)中实现了高效、可溶性的融合表达,表达量约30%.重组的蛋白质经亲和纯化至电泳纯,纯化后的hFKBP52显示出肽基脯氨基顺反异构酶活性.表明原核表达的hFKBP52具有类似于其天然蛋白质的生物学活性.

关 键 词:人FKBP52,基因克隆,原核表达,肽基脯氨基顺反异构酶
收稿时间:2000/4/17 0:00:00
修稿时间:2000年4月17日

The Gene Cloning, Expression and Bioactivity of the Human FKBP52
PEI Wu-Hong,HE Yong-Huai,CHEN Xing,LI Song and SHEN Bei-Fen.The Gene Cloning, Expression and Bioactivity of the Human FKBP52[J].Progress In Biochemistry and Biophysics,2001,28(2):236-239.
Authors:PEI Wu-Hong  HE Yong-Huai  CHEN Xing  LI Song and SHEN Bei-Fen
Institution:Beijing Institute of Basic Medical Sciences, Beijing 100850, China;Beijing Institute of Basic Medical Sciences, Beijing 100850, China;Beijing Institute of Basic Medical Sciences, Beijing 100850, China;Beijing Institute of pharmacology and toxicology, Beijing 100850, China;Beijing Institute of Basic Medical Sciences, Beijing 100850, China
Abstract:To obtain active hFKBP52 protein for screening novel neurotrophic drugs. Semi-nested and overlap PCR and affinity chromatography were used. hFKBP52 gene was cloned successfully from human fetal brain cDNA library, and then highly expressed (about 30%) as fusion protein in pET28a(+) vector system. The recombinant protein was purified as one band on SDS-PAGE. The purified hFKBP52 showed peptidyl-prolyl cis-trans isomerase (PPIase) activity, similar to the wild type.
Keywords:hFKBP52  gene clone  proyoatic expression  peptidyl-prolyl cis-trans isomerase
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