Evidence map›Paper›PMID 40781123›Full record

ArticleCommunications biology2025

A second photoactivatable state of the anion-conducting channelrhodopsin GtACR1 empowers persistent activity.

Kristin Labudda, Mohamad Javad Norahan, Lisa-Marie Hübner, Philipp Althoff, Klaus Gerwert, Mathias Lübben, Till Rudack, Carsten Kötting

Abstract read
In one paragraph

Article in Communications biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

8 authors.

Kristin LabuddaCenter for Protein Diagnostics (PRODI), Biospectroscopy, Ruhr University Bochum, Bochum, Germany.ORCID http://orcid.org/0000-0003-0548-3585
Mohamad Javad NorahanCenter for Protein Diagnostics (PRODI), Biospectroscopy, Ruhr University Bochum, Bochum, Germany.
Lisa-Marie HübnerCenter for Protein Diagnostics (PRODI), Biospectroscopy, Ruhr University Bochum, Bochum, Germany.
Philipp AlthoffCenter for Protein Diagnostics (PRODI), Biospectroscopy, Ruhr University Bochum, Bochum, Germany.
Klaus GerwertCenter for Protein Diagnostics (PRODI), Biospectroscopy, Ruhr University Bochum, Bochum, Germany.
Mathias LübbenCenter for Protein Diagnostics (PRODI), Biospectroscopy, Ruhr University Bochum, Bochum, Germany.
Till RudackStructural Bioinformatics Group, Regensburg Center for Biochemistry, Regensburg Center for Ultrafast Nanoscopy, University of Regensburg, Regensburg, Germany. till.rudack@ur.de.ORCID http://orcid.org/0000-0003-2693-9561
Carsten KöttingCenter for Protein Diagnostics (PRODI), Biospectroscopy, Ruhr University Bochum, Bochum, Germany. carsten.koetting@rub.de.ORCID http://orcid.org/0000-0002-3599-9657

Funding

Deutsche Forschungsgemeinschaft (German Research Foundation) GE 599/19-1Deutsche Forschungsgemeinschaft (German Research Foundation) GE 599/19-2Deutsche Forschungsgemeinschaft (German Research Foundation) GE 599/23-1
6 · The paper itself

Abstract

Optogenetics is a method to regulate cells, tissues and organisms using light. It is applied to study neurons and to develop diagnostic and therapeutic tools for neuron-related diseases. The cation-conducting channelrhodopsin ChR2 triggers photoinduced depolarization of neuronal cells but generates lower ion currents due to the syn-pathway of its branched photocycle. In contrast, the homologous anion-conducting ACR1 from Guillardia theta (GtACR1), exhibits high photocurrents. Here, we investigate the mechanistic cause for the observed high photocurrents in GtACR1 using FTIR spectroscopy. Unexpectedly, we discovered that the O intermediate of GtACR1 is photoactivable, allowing for fast and efficient channel reopening. Our vibrational spectra show a photocyclic reaction sequence after O excitation similar to the ground state photocycle but with slightly altered channel conformation and protonation states. Our results provide deeper insights into the gating mechanism of channelrhodopsins and pave the way to advance the development of optimized optogenetic tools in future.

Indexed as

ChannelrhodopsinsCryptophytaAnionsIon Channel GatingLightOptogeneticsSpectroscopy, Fourier Transform InfraredAnionsChannelrhodopsins

Identifiers

PMID40781123
PMCPMC12334634

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

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 Socratic graph.