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SRP、FtsY、DnaK 和 YidC 对于大肠杆菌尾部锚定膜蛋白 DjlC 和 Flk 的生物发生是必需的。

SRP, FtsY, DnaK and YidC Are Required for the Biogenesis of the E. coli Tail-Anchored Membrane Proteins DjlC and Flk.

机构信息

The Amsterdam Institute of Molecules, Medicines and Systems, VU University Amsterdam, De Boelelaan 1085, 1081, HV, Amsterdam, the Netherlands.

Department of Biochemistry and Biophysics, Center for Biomembrane Research, Stockholm University, Svante Arrhenius väg 16C, SE-106 91 Stockholm, Sweden.

出版信息

J Mol Biol. 2018 Feb 2;430(3):389-403. doi: 10.1016/j.jmb.2017.12.004. Epub 2017 Dec 12.

Abstract

Tail-anchored membrane proteins (TAMPs) are relatively simple membrane proteins characterized by a single transmembrane domain (TMD) at their C-terminus. Consequently, the hydrophobic TMD, which acts as a subcellular targeting signal, emerges from the ribosome only after termination of translation precluding canonical co-translational targeting and membrane insertion. In contrast to the well-studied eukaryotic TAMPs, surprisingly little is known about the cellular components that facilitate the biogenesis of bacterial TAMPs. In this study, we identify DjlC and Flk as bona fide Escherichia coli TAMPs and show that their TMDs are necessary and sufficient for authentic membrane targeting of the fluorescent reporter mNeonGreen. Using strains conditional for the expression of known E. coli membrane targeting and insertion factors, we demonstrate that the signal recognition particle (SRP), its receptor FtsY, the chaperone DnaK and insertase YidC are each required for efficient membrane localization of both TAMPs. A close association between the TMD of DjlC and Flk with both the Ffh subunit of SRP and YidC was confirmed by site-directed in vivo photo-crosslinking. In addition, our data suggest that the hydrophobicity of the TMD correlates with the dependency on SRP for efficient targeting.

摘要

尾部锚定膜蛋白(TAMPs)是相对简单的膜蛋白,其特征是在 C 末端有一个单一的跨膜结构域(TMD)。因此,疏水性的 TMD 作为亚细胞靶向信号,在翻译终止后才从核糖体中出现,这排除了典型的共翻译靶向和膜插入。与研究充分的真核 TAMPs 相比,关于促进细菌 TAMPs 生物发生的细胞成分,人们知之甚少。在这项研究中,我们鉴定出 DjlC 和 Flk 是真正的大肠杆菌 TAMPs,并表明它们的 TMD 对于荧光报告蛋白 mNeonGreen 的真实膜靶向是必要和充分的。使用已知的大肠杆菌膜靶向和插入因子表达条件菌株,我们证明信号识别颗粒(SRP)、其受体 FtsY、伴侣蛋白 DnaK 和插入酶 YidC 对于两种 TAMPs 的有效膜定位都是必需的。通过定点体内光交联实验证实了 DjlC 和 Flk 的 TMD 与 SRP 的 Ffh 亚基和 YidC 之间的密切关联。此外,我们的数据表明,TMD 的疏水性与对 SRP 进行有效靶向的依赖性相关。

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