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尾锚定(TA)蛋白膜插入的不同靶向途径。

Distinct targeting pathways for the membrane insertion of tail-anchored (TA) proteins.

作者信息

Favaloro Vincenzo, Spasic Milan, Schwappach Blanche, Dobberstein Bernhard

机构信息

Zentrum für Molekulare Biologie der Universität Heidelberg (ZMBH), DKFZ-ZMBH Allianz, Heidelberg, Germany.

出版信息

J Cell Sci. 2008 Jun 1;121(11):1832-40. doi: 10.1242/jcs.020321. Epub 2008 May 13.

Abstract

Tail-anchored (TA) proteins are characterised by a C-terminal transmembrane region that mediates post-translational insertion into the membrane of the endoplasmic reticulum (ER). We have investigated the requirements for membrane insertion of three TA proteins, RAMP4, Sec61beta and cytocrome b5. We show here that newly synthesised RAMP4 and Sec61beta can accumulate in a cytosolic, soluble complex with the ATPase Asna1 before insertion into ER-derived membranes. Membrane insertion of these TA proteins is stimulated by ATP, sensitive to redox conditions and blocked by alkylation of SH groups by N-ethylmaleimide (NEM). By contrast, membrane insertion of cytochrome b5 is not found to be mediated by Asna1, not stimulated by ATP and not affected by NEM or an oxidative environment. The Asna1-mediated pathway of membrane insertion of RAMP4 and Sec61beta may relate to functions of these proteins in the ER stress response.

摘要

尾锚定(TA)蛋白的特征是具有一个C端跨膜区域,该区域介导翻译后插入内质网(ER)膜。我们研究了三种TA蛋白RAMP4、Sec61β和细胞色素b5插入膜的条件。我们在此表明,新合成的RAMP4和Sec61β在插入ER衍生膜之前,可与ATP酶Asna1在胞质溶胶中形成可溶性复合物并积累。这些TA蛋白的膜插入受到ATP的刺激,对氧化还原条件敏感,并被N-乙基马来酰亚胺(NEM)对SH基团的烷基化所阻断。相比之下,未发现细胞色素b5的膜插入由Asna1介导,不受ATP刺激,也不受NEM或氧化环境的影响。RAMP4和Sec61β由Asna1介导的膜插入途径可能与这些蛋白在内质网应激反应中的功能有关。

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