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从人类疟原虫恶性疟原虫中分离并表达一个编码类cdc2蛋白激酶的基因。

Isolation and expression of a gene specifying a cdc2-like protein kinase from the human malaria parasite Plasmodium falciparum.

作者信息

Ross-Macdonald P B, Graeser R, Kappes B, Franklin R, Williamson D H

机构信息

National Institute for Medical Research, Mill Hill, London, England.

出版信息

Eur J Biochem. 1994 Mar 15;220(3):693-701. doi: 10.1111/j.1432-1033.1994.tb18670.x.

Abstract

A partially redundant oligonucleotide based on conserved protein sequences of cdk and cdc2-like proteins was used to isolate from genomic libraries of Plasmodium falciparum fragments of chromosome XIII carrying a 288-residue open-reading frame encoding a protein kinase sharing 57-58% identity with yeast p34cdc2. Based on sequence data, base composition and the striking similarity with other cdk and related proteins, four intervening sequences were identified. Their removal in vitro allowed expression of the gene, designated PfPK5, in Escherichia coli, the resulting product having kinase activity against casein and histone H1. Western blotting using a polyclonal antibody raised against the expressed protein showed that the kinase was located in the parasite's cytosol and was present in approximately constant amounts throughout the intra-erythrocytic asexual reproductive stage of the life cycle. The PSTAIRE region of the PfPK5 protein differs at three sites from that of p34cdc2, and the gene failed to complement cdc2/28 yeast mutants. However, Western blotting showed that the gene was not expressed in yeast, so this does not eliminate the possibility that it is the malarial version of cdc2.

摘要

基于细胞周期蛋白依赖性激酶(cdk)和类细胞分裂周期蛋白2(cdc2)保守蛋白序列的部分冗余寡核苷酸,用于从恶性疟原虫基因组文库中分离携带288个氨基酸开放阅读框的XIII号染色体片段,该开放阅读框编码一种蛋白激酶,与酵母p34cdc2具有57 - 58%的同源性。根据序列数据、碱基组成以及与其他cdk和相关蛋白的显著相似性,鉴定出四个内含子序列。在体外去除这些内含子后,使命名为PfPK5的基因在大肠杆菌中得以表达,产生的产物对酪蛋白和组蛋白H1具有激酶活性。使用针对表达蛋白产生的多克隆抗体进行的蛋白质印迹分析表明,该激酶位于疟原虫的胞质溶胶中,并且在整个红细胞内无性生殖阶段的生命周期中含量大致恒定。PfPK5蛋白的PSTAIRE区域与p34cdc2的PSTAIRE区域在三个位点存在差异,并且该基因不能互补cdc2/28酵母突变体。然而,蛋白质印迹分析表明该基因在酵母中不表达,所以这并不能排除它是疟原虫版本的cdc2的可能性。

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