Isospectral intermediates in the photochemical reaction cycle of anion channelrhodopsin GtACR1.


Journal

Biophysical journal
ISSN: 1542-0086
Titre abrégé: Biophys J
Pays: United States
ID NLM: 0370626

Informations de publication

Date de publication:
17 10 2023
Historique:
received: 24 04 2023
revised: 15 08 2023
accepted: 15 09 2023
pmc-release: 17 10 2024
medline: 23 10 2023
pubmed: 26 9 2023
entrez: 26 9 2023
Statut: ppublish

Résumé

The most effective tested optogenetic tools available for neuronal silencing are the light-gated anion channel proteins found in the cryptophyte alga Guillardia theta (GtACRs). Molecular mechanisms of GtACRs, including the photointermediates responsible for the open channel state, are of great interest for understanding their exceptional conductance. In this study, the photoreactions of GtACR1 and its D234N, A75E, and S97E mutants were investigated using multichannel time-resolved absorption spectroscopy. For each of the proteins, the analysis showed two early microsecond transitions between K-like and L-like forms and two late millisecond recovery steps. Spectral forms associated with potential molecular intermediates of the proteins were derived and their evolutions in time were analyzed. The results indicate the presence of isospectral intermediates in the photocycles and expand the range of potential intermediates responsible for the open channel state.

Identifiants

pubmed: 37749886
pii: S0006-3495(23)00586-6
doi: 10.1016/j.bpj.2023.09.009
pmc: PMC10598346
pii:
doi:

Substances chimiques

Channelrhodopsins 0
Anions 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

4091-4103

Subventions

Organisme : NEI NIH HHS
ID : R01 EY029343
Pays : United States
Organisme : NIGMS NIH HHS
ID : R35 GM140838
Pays : United States

Informations de copyright

Copyright © 2023. Published by Elsevier Inc.

Déclaration de conflit d'intérêts

Declaration of interests The authors declare no competing interests.

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Auteurs

Pamela Schleissner (P)

Department of Chemistry & Biochemistry, University of California Santa Cruz, Santa Cruz, California.

Istvan Szundi (I)

Department of Chemistry & Biochemistry, University of California Santa Cruz, Santa Cruz, California.

Eefei Chen (E)

Department of Chemistry & Biochemistry, University of California Santa Cruz, Santa Cruz, California.

Hai Li (H)

Center for Membrane Biology, Department of Biochemistry & Molecular Biology, University of Texas Health Science Center at Houston McGovern Medical School, Houston, Texas.

John L Spudich (JL)

Center for Membrane Biology, Department of Biochemistry & Molecular Biology, University of Texas Health Science Center at Houston McGovern Medical School, Houston, Texas.

David S Kliger (DS)

Department of Chemistry & Biochemistry, University of California Santa Cruz, Santa Cruz, California. Electronic address: kliger@ucsc.edu.

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Classifications MeSH