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尾部锚定膜蛋白靶向和插入的机制。

Mechanisms of Tail-Anchored Membrane Protein Targeting and Insertion.

机构信息

Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, California 91125; email:

出版信息

Annu Rev Cell Dev Biol. 2017 Oct 6;33:417-438. doi: 10.1146/annurev-cellbio-100616-060839.

Abstract

Proper localization of membrane proteins is essential for the function of biological membranes and for the establishment of organelle identity within a cell. Molecular machineries that mediate membrane protein biogenesis need to not only achieve a high degree of efficiency and accuracy, but also prevent off-pathway aggregation events that can be detrimental to cells. The posttranslational targeting of tail-anchored proteins (TAs) provides tractable model systems to probe these fundamental issues. Recent advances in understanding TA-targeting pathways reveal sophisticated molecular machineries that drive and regulate these processes. These findings also suggest how an interconnected network of targeting factors, cochaperones, and quality control machineries together ensures robust membrane protein biogenesis.

摘要

膜蛋白的正确定位对于生物膜的功能和细胞内细胞器的身份建立至关重要。介导膜蛋白生物发生的分子机制不仅需要达到高度的效率和准确性,还需要防止可能对细胞有害的偏离途径的聚集事件。翻译后靶向尾部锚定蛋白 (TA) 提供了易于研究的模型系统来探究这些基本问题。最近在理解 TA 靶向途径方面的进展揭示了驱动和调节这些过程的复杂分子机制。这些发现还表明,靶向因子、共伴侣和质量控制机制的相互关联网络如何共同确保稳健的膜蛋白生物发生。

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