| Literature DB >> 33973334 |
Johanna Becker-Baldus1, Alexander Leeder2, Lynda J Brown2, Richard C D Brown2, Christian Bamann3, Clemens Glaubitz4.
Abstract
Channelrhodopsin-2 (ChR2) is a light-gated cation channel and was used to lay the foundations of optogenetics. Its dark state X-ray structure has been determined in 2017 for the wild-type, which is the prototype for all other ChR variants. However, the mechanistic understanding of the channel function is still incomplete in terms of structural changes after photon absorption by the retinal chromophore and in the framework of functional models. Hence, detailed information needs to be collected on the dark state as well as on the different photointermediates. For ChR-2 detailed knowledge on the chromophore configuration in the different states is still missing and a consensus has not been achieved. Using DNP-enhanced solid-state MAS NMR spectroscopy on proteoliposome samples, we unambiguously determine the chromophore configuration in the desensitized state, and we show that this state occurs towards the end of the photocycle.Entities:
Keywords: channelrhodopsin; dynamic nuclear polarization; membrane proteins; photocycle; solid-state NMR spectroscopy
Year: 2021 PMID: 33973334 DOI: 10.1002/anie.202015797
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336