8YEJ

Cryo-EM structure of the channelrhodopsin GtCCR2 focused on the monomer

Summary for 8YEJ

• Entry DOI: 10.2210/pdb8yej/pdb
• EMDB information: 39197
• Descriptor: GtCCR2, RETINAL (3 entities in total)
• Functional Keywords: microbial rhodopsin, membrane protein
• Biological source: Guillardia theta CCMP2712
• Total number of polymer chains: 1
• Total formula weight: 53109.66

Authors

Tanaka, T.,Iida, W.,Sano, F.K.,Oda, K.,Shihoya, W.,Nureki, O. (deposition date: 2024-02-22, release date: 2024-09-04, Last modification date: 2024-10-02)

Primary citation

Tanaka, T.,Hososhima, S.,Yamashita, Y.,Sugimoto, T.,Nakamura, T.,Shigemura, S.,Iida, W.,Sano, F.K.,Oda, K.,Uchihashi, T.,Katayama, K.,Furutani, Y.,Tsunoda, S.P.,Shihoya, W.,Kandori, H.,Nureki, O.
The high-light-sensitivity mechanism and optogenetic properties of the bacteriorhodopsin-like channelrhodopsin GtCCR4.
Mol.Cell, 84:3530-3544.e6, 2024

PubMed 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.

PubMed: 39232582
DOI: 10.1016/j.molcel.2024.08.016

Experimental method

ELECTRON MICROSCOPY (2.86 Å)