共 88 条
Cotranslational sorting and processing of newly synthesized proteins in eukaryotes
被引:19
作者:

Gamerdinger, Martin
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h-index: 0
机构:
Univ Konstanz, Dept Biol, Mol Microbiol, D-78457 Constance, Germany Univ Konstanz, Dept Biol, Mol Microbiol, D-78457 Constance, Germany

Deuerling, Elke
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h-index: 0
机构:
Univ Konstanz, Dept Biol, Mol Microbiol, D-78457 Constance, Germany Univ Konstanz, Dept Biol, Mol Microbiol, D-78457 Constance, Germany
机构:
[1] Univ Konstanz, Dept Biol, Mol Microbiol, D-78457 Constance, Germany
关键词:
N-TERMINAL MODIFICATIONS;
MOLECULAR CHAPERONES;
STRUCTURAL BASIS;
RIBOSOME;
COMPLEX;
HSP70;
NAC;
MECHANISM;
REVEALS;
MPP11;
D O I:
10.1016/j.tibs.2023.10.003
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:
Ribosomes interact with a variety of different protein biogenesis factors that guide newly synthesized proteins to their native 3D shapes and cellular localization. Depending on the type of translated substrate, a distinct set of cotranslational factors must interact with the ribosome in a timely and coordinated manner to ensure proper protein biogenesis. While cytonuclear proteins require cotranslational maturation and folding factors, secretory proteins must be maintained in an unfolded state and processed cotranslationally by transport and membrane translocation factors. Here we explore the specific cotranslational processing steps for cytonuclear, secretory, and membrane proteins in eukaryotes and then discuss how the nascent polypeptide-associated complex (NAC) cotranslationally sorts these proteins into the correct protein biogenesis pathway.
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收藏
页码:105 / 118
页数:14
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