Evidence map›Paper›PMID 38811857›Full record

ArticleNature methods2024

A bistable inhibitory optoGPCR for multiplexed optogenetic control of neural circuits.

Jonas Wietek, Adrianna Nozownik, Mauro Pulin, Inbar Saraf-Sinik, Noa Matosevich, Raajaram Gowrishankar, Asaf Gat, Daniela Malan, Bobbie J Brown, Julien Dine and 22 more

Abstract read
In one paragraph

Article in Nature methods, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing 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

25 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Multicolor photoreactions of the red light-activated channelrhodopsin Chrimson.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  9. Review
  10. Article
  11. Risk reshapes amygdala representation of choice.bioRxiv : the preprint server for biology · 2025
    Article
  12. Article
  13. Review
  14. Article
  15. Optogenetic engineering for ion channel modulation.Current opinion in chemical biology · 2025
    Review
  16. Article
  17. Review
  18. Review
  19. Protein design accelerates the development and application of optogenetic tools.Computational and structural biotechnology journal · 2025
    Review
  20. The function of GPCRs in different bone cells.International journal of biological sciences · 2025
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

32 authors.

Jonas WietekDepartment of Brain Sciences, Weizmann Institute of Science, Rehovot, Israel. jonas.wietek@gmail.com.ORCID http://orcid.org/0000-0002-8079-7042
Adrianna NozownikCenter for Molecular Neurobiology, Hamburg, Germany.
Mauro PulinCenter for Molecular Neurobiology, Hamburg, Germany.ORCID http://orcid.org/0000-0001-6255-0276
Inbar Saraf-SinikDepartment of Brain Sciences, Weizmann Institute of Science, Rehovot, Israel.
Noa MatosevichSagol School of Neuroscience, Tel Aviv University, Tel Aviv, Israel.
Raajaram GowrishankarDepartment of Anesthesiology and Pain Medicine, University of Washington, Seattle, WA, USA.
Asaf GatDepartment of Brain Sciences, Weizmann Institute of Science, Rehovot, Israel.ORCID http://orcid.org/0009-0005-3336-2096
Daniela MalanInstitut für Physiologie I, University of Bonn, Bonn, Germany.
Bobbie J BrownWashington University Pain Center, Department of Anesthesiology, Washington University School of Medicine, St. Louis, MO, USA.
Julien DineDepartment of Brain Sciences, Weizmann Institute of Science, Rehovot, Israel.
Bibi Nusreen ImambocusLIMES-Institute, University of Bonn, Bonn, Germany.
Rivka LevyDepartment of Brain Sciences, Weizmann Institute of Science, Rehovot, Israel.
Kathrin SauterCenter for Molecular Neurobiology, Hamburg, Germany.
Anna LitvinDepartment of Brain Sciences, Weizmann Institute of Science, Rehovot, Israel.ORCID http://orcid.org/0000-0002-0420-0216
Noa RegevDepartment of Physiology and Pharmacology, Tel Aviv University, Tel Aviv, Israel.
Suraj SubramaniamDepartment of Brain Sciences, Weizmann Institute of Science, Rehovot, Israel.
Khalid AbreraDepartment of Anesthesiology and Pain Medicine, University of Washington, Seattle, WA, USA.
Dustin SummarliDepartment of Anesthesiology and Pain Medicine, University of Washington, Seattle, WA, USA.ORCID http://orcid.org/0009-0003-6637-0805
Eva Madeline GorenSagol School of Neuroscience, Tel Aviv University, Tel Aviv, Israel.
Gili MizrachiDepartment of Brain Sciences, Weizmann Institute of Science, Rehovot, Israel.
Eyal BittonDepartment of Brain Sciences, Weizmann Institute of Science, Rehovot, Israel.
Asaf BenjaminDepartment of Brain Sciences, Weizmann Institute of Science, Rehovot, Israel.ORCID http://orcid.org/0000-0003-3031-2008
Bryan A CopitsWashington University Pain Center, Department of Anesthesiology, Washington University School of Medicine, St. Louis, MO, USA.ORCID http://orcid.org/0000-0003-3732-890X
Philipp SasseInstitut für Physiologie I, University of Bonn, Bonn, Germany.ORCID http://orcid.org/0000-0002-8502-9472
Benjamin R RostGerman Center for Neurodegenerative Diseases (DZNE), Berlin, Germany.ORCID http://orcid.org/0000-0003-1906-0081
Dietmar SchmitzGerman Center for Neurodegenerative Diseases (DZNE), Berlin, Germany.
Michael R BruchasDepartment of Anesthesiology and Pain Medicine, University of Washington, Seattle, WA, USA.ORCID http://orcid.org/0000-0003-4713-7816
Peter SobaLIMES-Institute, University of Bonn, Bonn, Germany.ORCID http://orcid.org/0000-0002-6163-4686
Meital Oren-SuissaDepartment of Brain Sciences, Weizmann Institute of Science, Rehovot, Israel.ORCID http://orcid.org/0000-0001-9937-8326
Yuval NirSagol School of Neuroscience, Tel Aviv University, Tel Aviv, Israel.ORCID http://orcid.org/0000-0002-5433-6349
J Simon WiegertCenter for Molecular Neurobiology, Hamburg, Germany.ORCID http://orcid.org/0000-0003-0893-9349
Ofer YizharDepartment of Brain Sciences, Weizmann Institute of Science, Rehovot, Israel. ofer.yizhar@weizmann.ac.il.ORCID http://orcid.org/0000-0003-4228-1448

Funding

Next Generation Opto-GPCRs for Neuromodulatory ControlU01NS128537 · NINDS · UNIVERSITY OF WASHINGTON · PI Andre Berndt, Michael R. Bruchas · 2023 to 2026
$4.4M
Deutsche Forschungsgemeinschaft (German Research Foundation) EXC-2049 - 390688087, SPP 1665, SFB 958Deutsche Forschungsgemeinschaft (German Research Foundation) SFB 1315Deutsche Forschungsgemeinschaft (German Research Foundation) SPP 1926Deutsche Forschungsgemeinschaft (German Research Foundation) SPP1926EC | Horizon 2020 Framework Programme (EU Framework Programme for Research and Innovation H2020) ERC-2016-StG 714762EC | Horizon 2020 Framework Programme (EU Framework Programme for Research and Innovation H2020) ERC-2019-CoG 864353EC | Horizon 2020 Framework Programme (EU Framework Programme for Research and Innovation H2020) ERC-2019-STG 850784EC | Horizon 2020 Framework Programme (EU Framework Programme for Research and Innovation H2020) ERC CoG 819496EC | Horizon 2020 Framework Programme (EU Framework Programme for Research and Innovation H2020) H2020-RIA DEEPER 101016787EC | Horizon 2020 Framework Programme (EU Framework Programme for Research and Innovation H2020) SyG BrainPlay 810580European Molecular Biology Organization (EMBO) ALTF 378-2019Israel Science Foundation (ISF) ISF 1557/2NINDS NIH HHS U01 NS128537U.S. Department of Health & Human Services | NIH | Office of Extramural Research, National Institutes of Health (OER) 1U01NS128537-01
6 · The paper itself

Abstract

Information is transmitted between brain regions through the release of neurotransmitters from long-range projecting axons. Understanding how the activity of such long-range connections contributes to behavior requires efficient methods for reversibly manipulating their function. Chemogenetic and optogenetic tools, acting through endogenous G-protein-coupled receptor pathways, can be used to modulate synaptic transmission, but existing tools are limited in sensitivity, spatiotemporal precision or spectral multiplexing capabilities. Here we systematically evaluated multiple bistable opsins for optogenetic applications and found that the Platynereis dumerilii ciliary opsin (PdCO) is an efficient, versatile, light-activated bistable G-protein-coupled receptor that can suppress synaptic transmission in mammalian neurons with high temporal precision in vivo. PdCO has useful biophysical properties that enable spectral multiplexing with other optogenetic actuators and reporters. We demonstrate that PdCO can be used to conduct reversible loss-of-function experiments in long-range projections of behaving animals, thereby enabling detailed synapse-specific functional circuit mapping.

Indexed as

NeuronsOptogeneticsAnimalsHumansMiceOpsinsReceptors, G-Protein-CoupledSynapsesSynaptic TransmissionOpsinsReceptors, G-Protein-Coupled

Identifiers

PMID38811857
PMCPMC11239505

What Socratic holds

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LicenceCC BY
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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 Socratic graph.