Light-coupled cryo-plunger for time-resolved cryo-EM
[Display omitted] •A light-coupled cryo-plunger provides a flexible platform for time-resolved cryo-EM.•Coupling irradiation with high-speed mechanical plunge freezing enables temporal resolutions in the range of tens of milliseconds.•Ultraviolet irradiation from a light emitting diode robustly unca...
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Veröffentlicht in: | Journal of structural biology 2020-12, Vol.212 (3), p.107624-107624, Article 107624 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | [Display omitted]
•A light-coupled cryo-plunger provides a flexible platform for time-resolved cryo-EM.•Coupling irradiation with high-speed mechanical plunge freezing enables temporal resolutions in the range of tens of milliseconds.•Ultraviolet irradiation from a light emitting diode robustly uncages glutamate and protons.•On-grid photolysis of ‘caged protons’ activates acid-sensing ion channels and enables structure elucidation by single-particle cryo-EM.
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. |
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ISSN: | 1047-8477 1095-8657 |
DOI: | 10.1016/j.jsb.2020.107624 |