| Literature DB >> 32950604 |
Nate Yoder1, Farzad Jalali-Yazdi1, Sigrid Noreng1, Alexandra Houser1, Isabelle Baconguis1, Eric Gouaux2.
Abstract
Proteins are dynamic molecules that can undergo rapid conformational rearrangements in response to stimuli. These structural changes are often critical to protein function, and thus elucidating time-dependent conformational landscapes has been a long-standing goal of structural biology. To harness the power of single particle cryo-EM methods to enable 'time-resolved' structure determination, we have developed a light-coupled cryo-plunger that pairs flash-photolysis of caged ligands with rapid sample vitrification. The 'flash-plunger' consists of a high-power ultraviolet LED coupled with focusing optics and a motorized linear actuator, enabling the user to immobilize protein targets in vitreous ice within a programmable time window - as short as tens of milliseconds - after stimulus delivery. The flash-plunger is a simple, inexpensive and flexible tool to explore short-lived conformational states previously unobtainable by conventional sample preparation methods.Keywords: Cryo-EM; Cryo-electron microscopy; Manual cryo-plunger; Single particle; Time-resolved
Year: 2020 PMID: 32950604 DOI: 10.1016/j.jsb.2020.107624
Source DB: PubMed Journal: J Struct Biol ISSN: 1047-8477 Impact factor: 2.867