Quantifying elongation rhythm during full-length protein synthesis.
Quantifying elongation rhythm during full-length protein synthesis.
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DOI：
10.1021/ja405205c
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发表时间：
2013-07-31
影响因子：
15
通讯作者：
Cooperman, Barry S.
中科院分区：
文献类型：
--
作者：
Rosenblum, Gabriel;Chen, Chunlai;Kaur, Jaskiran;Cui, Xiaonan;Zhang, Haibo;Asahara, Haruichi;Chong, Shaorong;Smilansky, Zeev;Goldman, Yale E.;Cooperman, Barry S.
Pauses regulate the rhythm of ribosomal protein synthesis. Mutations disrupting even minor pauses can give rise to improperly formed proteins and human disease. Such minor pauses are difficult to characterize by ensemble methods, but can be readily examined by single-molecule (sm) approaches. Here we use smFRET to carry out real-time monitoring of the expression of a full-length protein, the green fluorescent protein variant Emerald GFP. We demonstrate significant correlations between measured elongation rates and codon and isoacceptor tRNA usage, and provide a quantitative estimate of the effect on elongation rate of replacing a codon recognizing an abundant tRNA with a synonymous codon cognate to a rarer tRNA. Our results suggest that tRNA selection plays an important general role in modulating the rates and rhythms of protein synthesis, potentially influencing simultaneous co-translational processes such as folding and chemical modification.
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