Evidence map›Paper›PMID 40533461›Full record

ArticleNature communications2025

Cryo-EM structure of a blue-shifted channelrhodopsin from Klebsormidium nitens.

Yuzhu Z Wang, Koki Natsume, Tatsuki Tanaka, Shoko Hososhima, Rintaro Tashiro, Fumiya K Sano, Hiroaki Akasaka, Satoshi P Tsunoda, Wataru Shihoya, Hideki Kandori and 1 more

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Blue-shifted ancyromonad channelrhodopsins for multiplex optogenetics.bioRxiv : the preprint server for biology · 2025
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Yuzhu Z WangDepartment of Biological Sciences, Graduate School of Science, The University of Tokyo, Tokyo, Japan.
Koki NatsumeDepartment of Life Science and Applied Chemistry, Nagoya Institute of Technology, Nagoya, Japan.
Tatsuki TanakaDepartment of Biological Sciences, Graduate School of Science, The University of Tokyo, Tokyo, Japan.
Shoko HososhimaDepartment of Life Science and Applied Chemistry, Nagoya Institute of Technology, Nagoya, Japan.
Rintaro TashiroDepartment of Life Science and Applied Chemistry, Nagoya Institute of Technology, Nagoya, Japan.
Fumiya K SanoDepartment of Biological Sciences, Graduate School of Science, The University of Tokyo, Tokyo, Japan.ORCID http://orcid.org/0000-0002-8965-788X
Hiroaki AkasakaDepartment of Biological Sciences, Graduate School of Science, The University of Tokyo, Tokyo, Japan.ORCID http://orcid.org/0000-0003-2118-0912
Satoshi P TsunodaDepartment of Life Science and Applied Chemistry, Nagoya Institute of Technology, Nagoya, Japan.ORCID http://orcid.org/0000-0003-3636-1521
Wataru ShihoyaDepartment of Biological Sciences, Graduate School of Science, The University of Tokyo, Tokyo, Japan. wtrshh9@gmail.com.ORCID http://orcid.org/0000-0003-4813-5740
Hideki KandoriDepartment of Life Science and Applied Chemistry, Nagoya Institute of Technology, Nagoya, Japan. kandori@nitech.ac.jp.ORCID http://orcid.org/0000-0002-4922-1344
Osamu NurekiDepartment of Biological Sciences, Graduate School of Science, The University of Tokyo, Tokyo, Japan. nureki@bs.s.u-tokyo.ac.jp.ORCID http://orcid.org/0000-0003-1813-7008

Funding

Japan Agency for Medical Research and Development (AMED) JP22ama121002MEXT | Japan Science and Technology Agency (JST) 20344981
6 · The paper itself

Abstract

Channelrhodopsins (ChRs) are light-gated ion channels and invaluable tools for optogenetic applications. Recent developments in multicolor optogenetics, in which different neurons are controlled by multiple colors of light simultaneously, have increased the demand for ChR mutants with more distant absorption wavelengths. Here we report the 2.7 Å-resolution cryo-electron microscopy structure of a ChR from Klebsormidium nitens (KnChR), which is one of the most blue-shifted ChRs. The structure elucidates the 6-s-cis configuration of the retinal chromophore, indicating its contribution to a distinctive blue shift in action spectra. The unique architecture of the C-terminal region reveals its role in the allosteric modulation of channel kinetics, enhancing our understanding of its functional dynamics. Employing a rational approach, we developed mutants with blue-shifted action spectra. Finally, we confirm that UV or deep-blue light can activate KnChR-transfected precultured neurons, expanding its utility in optogenetic applications. Our findings contribute valuable insights to advance optogenetic tools and enable refined capabilities in neuroscience experiments.

Indexed as

ChannelrhodopsinsAnimalsCryoelectron MicroscopyHumansLightModels, MolecularNeuronsOptogeneticsChannelrhodopsins

Identifiers

PMID40533461
PMCPMC12177036

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.