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Get3-Get4-Get5 蛋白复合物的相互作用表面和拓扑结构,涉及将尾部锚定蛋白靶向内质网。

Interaction surface and topology of Get3-Get4-Get5 protein complex, involved in targeting tail-anchored proteins to endoplasmic reticulum.

机构信息

Institute of Molecular Biology, Academia Sinica, Taipei 115, Taiwan.

出版信息

J Biol Chem. 2012 Feb 10;287(7):4783-9. doi: 10.1074/jbc.M111.318329. Epub 2011 Dec 21.

DOI:10.1074/jbc.M111.318329
PMID:22190685
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3281643/
Abstract

Recent work has uncovered the "GET system," which is responsible for endoplasmic reticulum targeting of tail-anchored proteins. Although structural information and the individual roles of most components of this system have been defined, the interactions and interplay between them remain to be elucidated. Here, we investigated the interactions between Get3 and the Get4-Get5 complex from Saccharomyces cerevisiae. We show that Get3 interacts with Get4-Get5 via an interface dominated by electrostatic forces. Using isothermal titration calorimetry and small-angle x-ray scattering, we further demonstrate that the Get3 homodimer interacts with two copies of the Get4-Get5 complex to form an extended conformation in solution.

摘要

最近的研究揭示了“GET 系统”,该系统负责尾部锚定蛋白的内质网靶向。尽管已经确定了该系统的大多数组件的结构信息和个别作用,但它们之间的相互作用和相互作用仍有待阐明。在这里,我们研究了酿酒酵母中 Get3 和 Get4-Get5 复合物之间的相互作用。我们表明,Get3 通过主要由静电相互作用控制的界面与 Get4-Get5 相互作用。使用等温滴定量热法和小角 X 射线散射,我们进一步证明 Get3 同源二聚体与两个 Get4-Get5 复合物相互作用,在溶液中形成延伸构象。

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J Biol Chem. 2012 Feb 10;287(7):4783-9. doi: 10.1074/jbc.M111.318329. Epub 2011 Dec 21.
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Endoplasmic reticulum membrane receptors of the GET pathway are conserved throughout eukaryotes.GET 途径的内质网膜受体在真核生物中是保守的。
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Differential gradients of interaction affinities drive efficient targeting and recycling in the GET pathway.相互作用亲和力的差异梯度驱动GET途径中的高效靶向和循环利用。
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Structural and functional characterization of ybr137wp implicates its involvement in the targeting of tail-anchored proteins to membranes.ybr137wp 的结构和功能特征表明其参与了将尾部锚定蛋白靶向到膜上。
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本文引用的文献

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A structural model of the Sgt2 protein and its interactions with chaperones and the Get4/Get5 complex. Sgt2 蛋白结构模型及其与伴侣蛋白和 Get4/Get5 复合物的相互作用。
J Biol Chem. 2011 Sep 30;286(39):34325-34. doi: 10.1074/jbc.M111.277798. Epub 2011 Aug 10.
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Structural basis for tail-anchored membrane protein biogenesis by the Get3-receptor complex.Get3 受体复合物介导的尾部锚定膜蛋白生物发生的结构基础。
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Cooperative and independent activities of Sgt2 and Get5 in the targeting of tail-anchored proteins. Sgt2 和 Get5 在靶向尾部锚定蛋白中的合作和独立活动。
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A chaperone cascade sorts proteins for posttranslational membrane insertion into the endoplasmic reticulum.伴侣蛋白复合物通过级联反应对蛋白质进行分类,以便将其进行翻译后插入内质网的膜中。
Mol Cell. 2010 Oct 8;40(1):159-71. doi: 10.1016/j.molcel.2010.08.038. Epub 2010 Sep 16.
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Structural characterization of the Get4/Get5 complex and its interaction with Get3.Get4/Get5 复合物的结构特征及其与 Get3 的相互作用。
Proc Natl Acad Sci U S A. 2010 Jul 6;107(27):12127-32. doi: 10.1073/pnas.1006036107. Epub 2010 Jun 16.
9
Crystal structure of Get4-Get5 complex and its interactions with Sgt2, Get3, and Ydj1.Get4-Get5 复合物的晶体结构及其与 Sgt2、Get3 和 Ydj1 的相互作用。
J Biol Chem. 2010 Mar 26;285(13):9962-9970. doi: 10.1074/jbc.M109.087098. Epub 2010 Jan 27.
10
Structural insight into the membrane insertion of tail-anchored proteins by Get3.Get3 介导的尾部锚定蛋白插入膜结构的结构洞察
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