EMD-39198

Single-particle
2.73 Å
EMD-39198 Deposition: 22/02/2024
Map released: 04/09/2024
Last modified: 06/11/2024
Overview 3D View Sample Experiment Validation Volume Browser Additional data Links
Overview 3D View Sample Experiment Validation Volume Browser Additional data Links

EMD-39198

Cryo-EM structure of the channelrhodopsin GtCCR2

EMD-39198

Single-particle
2.73 Å
EMD-39198 Deposition: 22/02/2024
Map released: 04/09/2024
Last modified: 06/11/2024
Overview 3D View Sample Experiment Validation Volume Browser Additional data Links
Sample Organism: Guillardia theta, Guillardia theta CCMP2712
Sample: GtCCR2
Fitted models: 8yek (Avg. Q-score: 0.564)

Deposition Authors: Tanaka T , Iida W, Sano FK , Oda K , Shihoya W , Nureki O
The high-light-sensitivity mechanism and optogenetic properties of the bacteriorhodopsin-like channelrhodopsin GtCCR4.
PUBMED: 39232582
DOI: doi:10.1016/j.molcel.2024.08.016
ISSN: 1097-2765
ASTM: MOCEFL
Abstract:
Channelrhodopsins are microbial light-gated ion channels that can control the firing of neurons in response to light. Among several cation channelrhodopsins identified in Guillardia theta (GtCCRs), GtCCR4 has higher light sensitivity than typical channelrhodopsins. Furthermore, GtCCR4 shows superior properties as an optogenetic tool, such as minimal desensitization. Our structural analyses of GtCCR2 and GtCCR4 revealed that GtCCR4 has an outwardly bent transmembrane helix, resembling the conformation of activated G-protein-coupled receptors. Spectroscopic and electrophysiological comparisons suggested that this helix bend in GtCCR4 omits channel recovery time and contributes to high light sensitivity. An electrophysiological comparison of GtCCR4 and the well-characterized optogenetic tool ChRmine demonstrated that GtCCR4 has superior current continuity and action-potential spike generation with less invasiveness in neurons. We also identified highly active mutants of GtCCR4. These results shed light on the diverse structures and dynamics of microbial rhodopsins and demonstrate the strong optogenetic potential of GtCCR4.