Evidence map›Paper›PMID 35606397›Full record

ArticleNature communications2022

The unconventional activation of the muscarinic acetylcholine receptor M4R by diverse ligands.

Jingjing Wang, Meng Wu, Zhangcheng Chen, Lijie Wu, Tian Wang, Dongmei Cao, Huan Wang, Shenhui Liu, Yueming Xu, Fei Li and 6 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

16 citing papers in PubMed, 27 citations in OpenAlex.

  1. Extracellular nanobody screening using conformationally stable GPCR variants.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  2. Downstream Signaling of Muscarinic MPharmacology research & perspectives · 2025
    Article
  3. Discovering Key Activation Hotspots in the MJournal of the American Chemical Society · 2025
    Article
  4. Review
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. A Novel "Activation Switch" Motif Common to All Aminergic Receptors.Journal of chemical information and modeling · 2023
    Review
  13. Article
  14. Article
  15. Deep Learning Dynamic Allostery of G-Protein-Coupled Receptors.bioRxiv : the preprint server for biology · 2023
    Article
  16. Review
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

16 authors at 2 institutions in 1 country.

Jingjing Wang *iHuman Institute, ShanghaiTech University, 201210, Shanghai, China.
Meng Wu *iHuman Institute, ShanghaiTech University, 201210, Shanghai, China.
Zhangcheng Chen *State Key Laboratory of Molecular Biology, Shanghai Institute of Biochemistry and Cell Biology, Center for Excellence in Molecular Cell Science, Chinese Academy of Sciences, 200031, Shanghai, China.ORCID 0000-0001-5858-2769
Lijie WuiHuman Institute, ShanghaiTech University, 201210, Shanghai, China.
Tian WangiHuman Institute, ShanghaiTech University, 201210, Shanghai, China.
Dongmei CaoState Key Laboratory of Molecular Biology, Shanghai Institute of Biochemistry and Cell Biology, Center for Excellence in Molecular Cell Science, Chinese Academy of Sciences, 200031, Shanghai, China.
Huan WangiHuman Institute, ShanghaiTech University, 201210, Shanghai, China.
Shenhui LiuiHuman Institute, ShanghaiTech University, 201210, Shanghai, China.
Yueming XuiHuman Institute, ShanghaiTech University, 201210, Shanghai, China.
Fei LiiHuman Institute, ShanghaiTech University, 201210, Shanghai, China.
Junlin LiuiHuman Institute, ShanghaiTech University, 201210, Shanghai, China.
Na CheniHuman Institute, ShanghaiTech University, 201210, Shanghai, China.
Suwen ZhaoiHuman Institute, ShanghaiTech University, 201210, Shanghai, China.ORCID 0000-0001-5609-434X
Jianjun ChengiHuman Institute, ShanghaiTech University, 201210, Shanghai, China. chengjj@shanghaitech.edu.cn.ORCID 0000-0001-6065-2682
Sheng WangState Key Laboratory of Molecular Biology, Shanghai Institute of Biochemistry and Cell Biology, Center for Excellence in Molecular Cell Science, Chinese Academy of Sciences, 200031, Shanghai, China. wangsheng@sibcb.ac.cn.ORCID 0000-0003-4176-8844
Tian HuaiHuman Institute, ShanghaiTech University, 201210, Shanghai, China. huatian@shanghaitech.edu.cn.ORCID 0000-0002-6132-2068
ShanghaiTech University · CNChinese Academy of Sciences · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Muscarinic acetylcholine receptors (mAChRs) respond to the neurotransmitter acetylcholine and play important roles in human nervous system. Muscarinic receptor 4 (M4R) is a promising drug target for treating neurological and mental disorders, such as Alzheimer's disease and schizophrenia. However, the lack of understanding on M4R's activation by subtype selective agonists hinders its therapeutic applications. Here, we report the structural characterization of M4R selective allosteric agonist, compound-110, as well as agonist iperoxo and positive allosteric modulator LY2119620. Our cryo-electron microscopy structures of compound-110, iperoxo or iperoxo-LY2119620 bound M4R-G

Indexed as

Muscarinic AgonistsReceptors, MuscarinicAllosteric RegulationAnimalsCryoelectron MicroscopyHumansLigandsMiceLigandsMuscarinic AgonistsReceptors, Muscarinic

Identifiers

PMID35606397
PMCPMC9126879
OpenAlexW4281392846

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.