| Literature DB >> 27178840 |
Abstract
As high-resolution cryogenic electron microscopy (cryo-EM) structures of ribosomes proliferate, at resolutions that allow atomic interactions to be visualized, this article attempts to give a perspective on the way research on ribosome structure and dynamics may be headed, and particularly the new opportunities we have gained through recent advances in cryo-EM. It is pointed out that single-molecule FRET and cryo-EM form natural complements in the characterization of ribosome dynamics and transitions among equilibrating states of in vitro translational systems.Entities:
Keywords: cryo-EM; smFRET; time-resolved methods; translation
Mesh:
Year: 2016 PMID: 27178840 PMCID: PMC5010980 DOI: 10.1016/j.jmb.2016.04.034
Source DB: PubMed Journal: J Mol Biol ISSN: 0022-2836 Impact factor: 5.469