Evidence map›Paper›PMID 39738009›Full record

ArticleNature communications2024

Photoswitch dissociation from a G protein-coupled receptor resolved by time-resolved serial crystallography.

Hannah Glover, Torben Saßmannshausen, Quentin Bertrand, Matilde Trabuco, Chavdar Slavov, Arianna Bacchin, Fabio Andres, Yasushi Kondo, Robin Stipp, Maximilian Wranik and 14 more

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Review
  2. Article
  3. Structural Mechanism of an Efficacy Photoswitch Targeting the βAngewandte Chemie (International ed. in English) · 2026
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. 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

24 authors.

Hannah GloverPSI Center for Life Sciences, Villigen PSI, Switzerland.ORCID 0000-0001-6558-8878
Torben SaßmannshausenInstitute of Physical and Theoretical Chemistry, Goethe University, Frankfurt, Germany.
Quentin BertrandPSI Center for Life Sciences, Villigen PSI, Switzerland.ORCID 0000-0003-3476-1775
Matilde TrabucoleadXpro AG, Park Innovaare, Villigen PSI, Switzerland.ORCID 0000-0001-9234-8685
Chavdar SlavovInstitute of Physical and Theoretical Chemistry, Goethe University, Frankfurt, Germany.ORCID 0000-0001-9441-0243
Arianna BacchinleadXpro AG, Park Innovaare, Villigen PSI, Switzerland.
Fabio AndresleadXpro AG, Park Innovaare, Villigen PSI, Switzerland.
Yasushi KondoPSI Center for Life Sciences, Villigen PSI, Switzerland.ORCID 0000-0003-2131-575X
Robin StippPSI Center for Life Sciences, Villigen PSI, Switzerland.
Maximilian WranikPSI Center for Life Sciences, Villigen PSI, Switzerland.
Georgii KhusainovPSI Center for Life Sciences, Villigen PSI, Switzerland.
Melissa CarrilloPSI Center for Life Sciences, Villigen PSI, Switzerland.ORCID 0000-0002-0744-4486
Demet KekilliPSI Center for Life Sciences, Villigen PSI, Switzerland.
Jie NanMaxIV Laboratory, Lund University, Lund, Sweden.
Ana GonzalezMaxIV Laboratory, Lund University, Lund, Sweden.ORCID 0000-0001-8858-399X
Robert ChengleadXpro AG, Park Innovaare, Villigen PSI, Switzerland.ORCID 0000-0001-7564-1230
Werner NeidhartleadXpro AG, Park Innovaare, Villigen PSI, Switzerland.
Tobias WeinertPSI Center for Life Sciences, Villigen PSI, Switzerland.ORCID 0000-0002-0339-3722
Filip LeonarskiPSI Center for Photon Sciences, Villigen PSI, Switzerland.
Florian DworkowskiPSI Center for Photon Sciences, Villigen PSI, Switzerland.ORCID 0000-0001-5004-8684
Michal KepaPSI Center for Life Sciences, Villigen PSI, Switzerland.ORCID 0000-0002-4045-3990
Josef WachtveitlInstitute of Physical and Theoretical Chemistry, Goethe University, Frankfurt, Germany.ORCID 0000-0002-8496-8240
Michael HennigleadXpro AG, Park Innovaare, Villigen PSI, Switzerland.ORCID 0000-0002-1839-2351
Joerg StandfussPSI Center for Life Sciences, Villigen PSI, Switzerland. joerg.standfuss@psi.ch.ORCID 0000-0001-8825-386X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

G protein-coupled receptors (GPCRs) are the largest family of cell surface receptors in humans. The binding and dissociation of ligands tunes the inherent conformational flexibility of these important drug targets towards distinct functional states. Here we show how to trigger and resolve protein-ligand interaction dynamics within the human adenosine A

Indexed as

Receptor, Adenosine A2ABinding SitesCrystallography, X-RayHumansLigandsProtein BindingProtein ConformationReceptors, G-Protein-CoupledADORA2A protein, humanLigandsReceptor, Adenosine A2AReceptors, G-Protein-Coupled

Identifiers

PMID39738009
PMCPMC11686364

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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 OpenQuestion graph.