Single-Molecule Fluorescence Applied to Translation

被引:22
|
作者
Prabhakar, Arjun [1 ,2 ]
Puglisi, Elisabetta Viani [1 ]
Puglisi, Joseph D. [1 ]
机构
[1] Stanford Univ, Sch Med, Dept Struct Biol, Stanford, CA 94305 USA
[2] Stanford Univ, Program Biophys, Stanford, CA 94305 USA
来源
COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY | 2019年 / 11卷 / 01期
基金
美国国家卫生研究院;
关键词
ESCHERICHIA-COLI RIBOSOMES; RELEASE FACTOR RF3; AMINOACYL-TRANSFER-RNA; NUCLEOTIDE EXCHANGE; KINETIC MECHANISM; GTP HYDROLYSIS; IN-VITRO; L1; STALK; PROTEIN; TERMINATION;
D O I
10.1101/cshperspect.a032714
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Single-molecule fluorescence methods have illuminated the dynamics of the translational machinery. Structural and bulk biochemical experiments have provided detailed atomic and global mechanistic views of translation, respectively. Single-molecule studies of translation have bridged these views by temporally connecting the conformational and compositional states defined from structural data within the mechanistic framework of translation produced from biochemical studies. Here, we discuss the context for applying different single-molecule fluorescence experiments, and present recent applications to studying prokaryotic and eukaryotic translation. We underscore the power of observing single translating ribosomes to delineate and sort complex mechanistic pathways during initiation and elongation, and discuss future applications of current and improved technologies.
引用
收藏
页数:17
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