A pause for thought along the co-translational folding pathway

被引:265
作者
Komar, Anton A. [1 ,2 ]
机构
[1] Cleveland State Univ, Ctr Gene Regulat Hlth & Dis, Cleveland, OH 44115 USA
[2] Cleveland State Univ, Dept Biol Geol & Environm Sci, Cleveland, OH 44115 USA
关键词
SYNONYMOUS CODON USAGE; NONUNIFORM SIZE DISTRIBUTION; PEPTIDYL-TRANSFER-RNA; CELL-FREE SYSTEM; ESCHERICHIA-COLI; IN-VIVO; MESSENGER-RNA; MOLECULAR CHAPERONES; FIREFLY LUCIFERASE; POLYPEPTIDE-CHAINS;
D O I
10.1016/j.tibs.2008.10.002
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
A unifying concept that combines the basic features governing self-organization of proteins into complex three-dimensional structures in vitro and in vivo is still lacking. Recent experimental results and theoretical in silico modeling studies provide evidence showing that mRNA might contain an additional layer of information, beyond the amino acid sequence, that fine-tunes in vivo protein folding, which is largely believed to start as a co-translational process. These findings indicate that translation kinetics might direct the co-translational folding pathway and that translational pausing at rare codons might provide a time delay to enable independent and sequential folding of the defined portions of the nascent polypeptide emerging from the ribosome.
引用
收藏
页码:16 / 24
页数:9
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