Ribosome dynamics and tRNA movement by time-resolved electron cryomicroscopy

被引:311
作者
Fischer, Niels [1 ]
Konevega, Andrey L. [2 ,3 ]
Wintermeyer, Wolfgang [2 ]
Rodnina, Marina V. [2 ]
Stark, Holger [1 ]
机构
[1] Max Planck Inst Biophys Chem, Elect Cryomicroscopy Grp 3D, D-37077 Gottingen, Germany
[2] Max Planck Inst Biophys Chem, Dept Phys Biochem, D-37077 Gottingen, Germany
[3] Petersburg Nucl Phys Inst, Gatchina 188300, Russia
关键词
ELONGATION-FACTOR-G; ESCHERICHIA-COLI RIBOSOMES; MESSENGER-RNA; L1; STALK; INTERMEDIATE STATES; ANGSTROM RESOLUTION; CRYSTAL-STRUCTURE; SINGLE RIBOSOMES; GTP HYDROLYSIS; HYBRID STATES;
D O I
10.1038/nature09206
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The translocation step of protein synthesis entails large-scale rearrangements of the ribosome-transfer RNA (tRNA) complex. Here we have followed tRNA movement through the ribosome during translocation by time-resolved single-particle electron cryomicroscopy (cryo-EM). Unbiased computational sorting of cryo-EM images yielded 50 distinct three-dimensional reconstructions, showing the tRNAs in classical, hybrid and various novel intermediate states that provide trajectories and kinetic information about tRNA movement through the ribosome. The structures indicate how tRNA movement is coupled with global and local conformational changes of the ribosome, in particular of the head and body of the small ribosomal subunit, and show that dynamic interactions between tRNAs and ribosomal residues confine the path of the tRNAs through the ribosome. The temperature dependence of ribosome dynamics reveals a surprisingly flat energy landscape of conformational variations at physiological temperature. The ribosome functions as a Brownian machine that couples spontaneous conformational changes driven by thermal energy to directed movement.
引用
收藏
页码:329 / 333
页数:5
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