Translation at the single-molecule level

被引:93
|
作者
Marshall, R. Andrew [1 ]
Aitken, Colin Echeverria [2 ]
Dorywalska, Magdalena [3 ]
Puglisi, Joseph D. [3 ,4 ]
机构
[1] Stanford Univ, Sch Med, Dept Chem, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Biophys Program, Stanford, CA 94305 USA
[3] Stanford Univ, Sch Med, Dept Biol Struct, Stanford, CA 94305 USA
[4] Stanford Univ, Sch Med, Stanford Magnet Resonance Lab, Stanford, CA 94305 USA
关键词
FRET; hybrid state; optical tweezers; protein synthesis; ribosome; tRNA selection;
D O I
10.1146/annurev.biochem.77.070606.101431
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
Decades of studies have established translation as a multistep, multicomponent process that requires intricate communication to achieve high levels of speed, accuracy, and regulation. A crucial next step in understanding translation is to reveal the functional significance of the large-scale motions implied by static ribosome structures. This requires determining the trajectories, timescales, forces, and biochemical signals that underlie these dynamic conformational changes. Single-molecule methods have emerged as important tools for the characterization of motion in complex systems, including translation. In this review, we chronicle the key discoveries in this nascent field, which have demonstrated the power and promise of single-molecule techniques in the study of translation.
引用
收藏
页码:177 / 203
页数:27
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