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无辅助的膜插入作为ΔpH/Tat依赖性蛋白质转运的起始步骤。

Unassisted membrane insertion as the initial step in DeltapH/Tat-dependent protein transport.

作者信息

Hou Bo, Frielingsdorf Stefan, Klösgen Ralf Bernd

机构信息

Institut für Pflanzenphysiologie, Martin-Luther-Universität Halle-Wittenberg, Weinbergweg 10, D-06120 Halle (Saale), Germany.

出版信息

J Mol Biol. 2006 Feb 3;355(5):957-67. doi: 10.1016/j.jmb.2005.11.029. Epub 2005 Nov 28.

Abstract

In the thylakoid membrane of chloroplasts as well as in the cytoplasmic membrane of bacteria, the DeltapH/Tat-dependent protein transport pathway is responsible for the translocation of folded proteins. Using the chimeric 16/23 protein as model substrate in thylakoid transport experiments, we dissected the transport process into several distinct steps that are characterized by specific integral translocation intermediates. Formation of the early translocation intermediate Ti-1, which still exposes the N and the C terminus to the stroma, is observed with thylakoids pretreated with (i) solutions of chaotropic salts or alkaline pH, (ii) protease, or (iii) antibodies raised against TatA, TatB, or TatC. Membrane insertion takes place even into liposomes, demonstrating that proteinaceous components are not required. This suggests that Tat-dependent transport may be initiated by the unassisted insertion of the substrate into the lipid bilayer, and that interaction with the Tat translocase takes place only in later stages of the process.

摘要

在叶绿体的类囊体膜以及细菌的细胞质膜中,ΔpH/Tat 依赖性蛋白质转运途径负责折叠蛋白的转运。在类囊体转运实验中,使用嵌合 16/23 蛋白作为模型底物,我们将转运过程分解为几个不同的步骤,这些步骤的特征是特定的完整转运中间体。在用(i)离液盐溶液或碱性 pH 溶液、(ii)蛋白酶或(iii)针对 TatA、TatB 或 TatC 产生的抗体预处理的类囊体中,观察到早期转运中间体 Ti-1 的形成,该中间体仍将 N 端和 C 端暴露于基质。膜插入甚至发生在脂质体中,这表明不需要蛋白质成分。这表明 Tat 依赖性转运可能由底物在脂质双层中的无辅助插入启动,并且与 Tat 转运体的相互作用仅在该过程的后期发生。

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