Gu Yongqing
School of Medicine, Shihezi University, Shihezi 832002, China.
Sheng Wu Gong Cheng Xue Bao. 2009 Feb;25(2):268-73.
Pif1 subfamily helicase is conserved from yeast to humans with a lot of cellular functions. In order to elucidate the function of human PIF1 helicase from biochemical level, we cloned human PIF1 gene by PCR from HeLa cell cDNA library. We co-transformed a pMStRNA1 plasmid encoding rare tRNA codons and a plasmid encoding molecular chaperon to greatly enhance the overexpression of human PIF1 protein. Finally we purified full-length PIF1 helicase by column chromatograph carried out at 4 degrees C using fast protein liquid chromatograph (FPLC) system. The human PIF1 protein was purified in enough quantity for detailed biochemical analysis. Biochemical assay showed that PIF1 had ATPase activity and helicase activity. The purification and biochemical properties analysis of human PIF1 helicase will allow us to understand how, at the molecular and mechanistic level, this conserved helicase operates in the cell.
Pif1亚家族解旋酶从酵母到人类都高度保守,具有多种细胞功能。为了从生化水平阐明人类PIF1解旋酶的功能,我们通过PCR从HeLa细胞cDNA文库中克隆了人类PIF1基因。我们共转化了一个编码稀有tRNA密码子的pMStRNA1质粒和一个编码分子伴侣的质粒,以极大地增强人类PIF1蛋白的过表达。最后,我们使用快速蛋白质液相色谱(FPLC)系统在4摄氏度下通过柱色谱法纯化了全长PIF1解旋酶。纯化得到了足够量的人类PIF1蛋白用于详细的生化分析。生化分析表明,PIF1具有ATP酶活性和解旋酶活性。人类PIF1解旋酶的纯化及生化特性分析将使我们能够在分子和机制层面了解这种保守的解旋酶在细胞中的作用方式。