Evidence map›Paper›PMID 37252352›Full record

ArticleACS central science2023

Conformational Dynamics of the Activated GLP-1 Receptor-G

Shijia Yuan, Lisha Xia, Chenxi Wang, Fan Wu, Bingjie Zhang, Chen Pan, Zhiran Fan, Xiaoguang Lei, Raymond C Stevens, Andrej Sali and 2 more

Open access · diamondAbstract read
In one paragraph

Article in ACS central science, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.8field-weighted citation impact, top 9% of its field
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

12 citing papers in PubMed, 20 citations in OpenAlex.

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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

12 authors at 5 institutions in 2 countries.

Shijia YuaniHuman Institute, ShanghaiTech University, Shanghai 201210, China.ORCID https://orcid.org/0000-0002-2008-9933
Lisha XiaiHuman Institute, ShanghaiTech University, Shanghai 201210, China.
Chenxi WangiHuman Institute, ShanghaiTech University, Shanghai 201210, China.
Fan WuStructure Therapeutics, South San Francisco, California 94080, United States.
Bingjie ZhangiHuman Institute, ShanghaiTech University, Shanghai 201210, China.
Chen PanNational Facility for Protein Science in Shanghai, Shanghai Advanced Research Institute, Chinese Academy of Science, Shanghai 201210, China.
Zhiran FanBiocreater (WuHan) Biotechnology Co., Ltd, Wuhan 430075, China.
Xiaoguang LeiBeijing National Laboratory for Molecular Sciences, State Key Laboratory of Natural and Biomimetic Drugs, Key Laboratory of Bioorganic Chemistry and Molecular Engineering of Ministry of Education, Department of Chemical Biology, College of Chemistry and Molecular Engineering, Peking-Tsinghua Center for Life Sciences, Peking University, Beijing 100871, China.ORCID https://orcid.org/0000-0002-0380-8035
Raymond C StevensiHuman Institute, ShanghaiTech University, Shanghai 201210, China.
Andrej SaliQuantitative Biosciences Institute, University of California, San Francisco, San Francisco, California 94143, United States.ORCID https://orcid.org/0000-0003-0435-6197
Liping SuniHuman Institute, ShanghaiTech University, Shanghai 201210, China.
Wenqing ShuiiHuman Institute, ShanghaiTech University, Shanghai 201210, China.ORCID https://orcid.org/0000-0002-5245-2477
ShanghaiTech University · CNPeking University · CNShanghai Advanced Research Institute · CNUniversity of California, San Francisco · USWuhan Institute of Bioengineering · CN

Funding

TR&D Project 4. The Imaging Stage: Multiscale Spatiotemporal Modeling of Macromolecular Systems in Cellular NeighborhoodsP41GM109824 · NIGMS · ROCKEFELLER UNIVERSITY · PI ROUT, MICHAEL P · 2014 to 2023
$18.8M
NIGMS NIH HHS P41 GM109824
6 · The paper itself

Abstract

Despite advances in characterizing the structures and functions of G protein-coupled receptors (GPCRs), our understanding of GPCR activation and signaling is still limited by the lack of information on conformational dynamics. It is particularly challenging to study the dynamics of GPCR complexes with their signaling partners because of their transient nature and low stability. Here, by combining cross-linking mass spectrometry (CLMS) with integrative structure modeling, we map the conformational ensemble of an activated GPCR-G protein complex at near-atomic resolution. The integrative structures describe heterogeneous conformations for a high number of potential alternative active states of the GLP-1 receptor-G

Identifiers

PMID37252352
PMCPMC10214531
OpenAlexW4366975489

What OpenQuestion 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 OpenQuestion graph.