Fidelity of Cotranslational Protein Targeting to the Endoplasmic Reticulum

被引:16
|
作者
Hsieh, Hao-Hsuan [1 ]
Shan, Shu-ou [1 ]
机构
[1] CALTECH, Div Chem & Chem Engn, Pasadena, CA 91125 USA
基金
美国国家科学基金会;
关键词
protein targeting; signal recognition particle; nascent polypeptide-associated complex; ribosome; endoplasmic reticulum; membrane proteins; fidelity; SIGNAL RECOGNITION PARTICLE; POLYPEPTIDE-ASSOCIATED COMPLEX; SEQUENCE RECOGNITION; ELONGATION ARREST; BETA-NAC; MEMBRANE ASSOCIATION; TRANSLATING RIBOSOME; NASCENT PREPROLACTIN; CRYSTAL-STRUCTURE; STRUCTURAL BASIS;
D O I
10.3390/ijms23010281
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Fidelity of protein targeting is essential for the proper biogenesis and functioning of organelles. Unlike replication, transcription and translation processes, in which multiple mechanisms to recognize and reject noncognate substrates are established in energetic and molecular detail, the mechanisms by which cells achieve a high fidelity in protein localization remain incompletely understood. Signal recognition particle (SRP), a conserved pathway to mediate the localization of membrane and secretory proteins to the appropriate cellular membrane, provides a paradigm to understand the molecular basis of protein localization in the cell. In this chapter, we review recent progress in deciphering the molecular mechanisms and substrate selection of the mammalian SRP pathway, with an emphasis on the key role of the cotranslational chaperone NAC in preventing protein mistargeting to the ER and in ensuring the organelle specificity of protein localization.
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收藏
页数:15
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