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鉴定嗜热四膜虫14纳米细丝相关蛋白为延伸因子1α。

Identification of Tetrahymena 14-nm filament-associated protein as elongation factor 1 alpha.

作者信息

Kurasawa Y, Numata O, Katoh M, Hirano H, Chiba J, Watanabe Y

机构信息

Institute of Biological Sciences, University of Tsukuba, Ibaraki, Japan.

出版信息

Exp Cell Res. 1992 Nov;203(1):251-8. doi: 10.1016/0014-4827(92)90062-d.

Abstract

Tetrahymena 14-nm filament-forming protein has dual functions as a citrate synthase in mitochondria and as a cytoskeletal protein involved in oral morphogenesis and in pronuclear behavior during conjugation. By immunoblotting using monoclonal and polyclonal antibodies following two-dimensional gel electrophoresis, we demonstrated that the 14-nm filament protein fraction contained two 49-kDa proteins whose isoelectric points were 8.0 and 9.0; a monoclonal antibody (MAb) 26B4 and a polyclonal antibody 49KI reacted only to a pI 8.0 protein, while two other MAbs, 11B6 and 11B8, reacted only to a pI 9.0 protein. From the N-terminal amino acid sequences, the pI 8.0 protein was identified as the previously reported 14-nm filament-forming protein/citrate synthase, but the pI 9.0 protein N-terminal sequence had no similarity with that of the pI 8.0 protein. The pI 9.0 protein is considered to be a 14-nm filament-associated protein since the pI 9.0 protein copurifies with the pI 8.0 protein during two cycles of an assembly and disassembly purification protocol. Cloning and sequencing the pI 9.0 protein gene from a Tetrahymena pyriformis cDNA library, we identified the pI 9.0 protein as elongation factor 1 alpha (EF-1 alpha) based on it sharing 73-76% sequence identity with EF-1 alpha from several species.

摘要

嗜热四膜虫14纳米丝形成蛋白具有双重功能,它既是线粒体中的柠檬酸合酶,又是参与口器形态发生以及接合过程中原核行为的细胞骨架蛋白。通过二维凝胶电泳后使用单克隆抗体和多克隆抗体进行免疫印迹分析,我们证明14纳米丝蛋白组分包含两种49千道尔顿的蛋白质,其等电点分别为8.0和9.0;单克隆抗体(MAb)26B4和多克隆抗体49KI仅与等电点为8.0的蛋白质发生反应,而另外两种单克隆抗体11B6和11B8仅与等电点为9.0的蛋白质发生反应。根据N端氨基酸序列,等电点为8.0的蛋白质被鉴定为先前报道的14纳米丝形成蛋白/柠檬酸合酶,但等电点为9.0的蛋白质N端序列与等电点为8.0的蛋白质没有相似性。由于在两轮组装和拆卸纯化方案中,等电点为9.0的蛋白质与等电点为8.0的蛋白质共纯化,因此等电点为9.0的蛋白质被认为是一种14纳米丝相关蛋白。从梨形四膜虫cDNA文库中克隆并测序等电点为9.0的蛋白质基因,基于它与几种物种的延伸因子1α(EF-1α)具有73 - 76%的序列同一性,我们将等电点为9.0的蛋白质鉴定为延伸因子1α(EF-1α)。

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