Evidence map›Paper›PMID 28302727›Full record

ArticleThe Journal of biological chemistry2017

Intersubunit physical couplings fostered by the left flipper domain facilitate channel opening of P2X4 receptors.

Jin Wang, Liang-Fei Sun, Wen-Wen Cui, Wen-Shan Zhao, Xue-Fei Ma, Bin Li, Yan Liu, Yang Yang, You-Min Hu, Li-Dong Huang and 5 more

Abstract read
In one paragraph

Article in The Journal of biological chemistry, 2017. 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
–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

12 citing papers in PubMed.

  1. A shared mechanism for TNP-ATP recognition by members of the P2X receptor family.Computational and structural biotechnology journal · 2024
    Article
  2. Article
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  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Druggable negative allosteric site of P2X3 receptors.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  11. Article
  12. 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

15 authors.

Jin WangFrom the Department of Pharmacology and Chemical Biology, Institute of Medical Sciences and Hongqiao International Institute of Medicine of Shanghai Tongren Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China.
Liang-Fei SunFrom the Department of Pharmacology and Chemical Biology, Institute of Medical Sciences and Hongqiao International Institute of Medicine of Shanghai Tongren Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China.
Wen-Wen CuiFrom the Department of Pharmacology and Chemical Biology, Institute of Medical Sciences and Hongqiao International Institute of Medicine of Shanghai Tongren Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China.
Wen-Shan ZhaoFrom the Department of Pharmacology and Chemical Biology, Institute of Medical Sciences and Hongqiao International Institute of Medicine of Shanghai Tongren Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China.
Xue-Fei MaFrom the Department of Pharmacology and Chemical Biology, Institute of Medical Sciences and Hongqiao International Institute of Medicine of Shanghai Tongren Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China.
Bin LiFrom the Department of Pharmacology and Chemical Biology, Institute of Medical Sciences and Hongqiao International Institute of Medicine of Shanghai Tongren Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China.
Yan LiuFrom the Department of Pharmacology and Chemical Biology, Institute of Medical Sciences and Hongqiao International Institute of Medicine of Shanghai Tongren Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China.
Yang YangFrom the Department of Pharmacology and Chemical Biology, Institute of Medical Sciences and Hongqiao International Institute of Medicine of Shanghai Tongren Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China.
You-Min HuFrom the Department of Pharmacology and Chemical Biology, Institute of Medical Sciences and Hongqiao International Institute of Medicine of Shanghai Tongren Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China.
Li-Dong HuangFrom the Department of Pharmacology and Chemical Biology, Institute of Medical Sciences and Hongqiao International Institute of Medicine of Shanghai Tongren Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China.
Xiao-Yang ChengFrom the Department of Pharmacology and Chemical Biology, Institute of Medical Sciences and Hongqiao International Institute of Medicine of Shanghai Tongren Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China.
Lingyong Lithe Department of Anesthesiology and Perioperative Medicine, University of Texas M.D. Anderson Cancer Center, Houston, Texas 77030.
Xiang-Yang Luthe College of Bioscience and Biotechnology, Hunan Agricultural University, Changsha 410128, China, and.
Yun Tianthe College of Bioscience and Biotechnology, Hunan Agricultural University, Changsha 410128, China, and tianyun79616@163.com.
Ye YuFrom the Department of Pharmacology and Chemical Biology, Institute of Medical Sciences and Hongqiao International Institute of Medicine of Shanghai Tongren Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China, yuye@shsmu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

P2X receptors are ATP-gated trimeric channels with important roles in diverse pathophysiological functions. A detailed understanding of the mechanism underlying the gating process of these receptors is thus fundamentally important and may open new therapeutic avenues. The left flipper (LF) domain of the P2X receptors is a flexible loop structure, and its coordinated motions together with the dorsal fin (DF) domain are crucial for the channel gating of the P2X receptors. However, the mechanism underlying the crucial role of the LF domain in the channel gating remains obscure. Here, we propose that the ATP-induced allosteric changes of the LF domain enable it to foster intersubunit physical couplings among the DF and two lower body domains, which are pivotal for the channel gating of P2X4 receptors. Metadynamics analysis indicated that these newly established intersubunit couplings correlate well with the ATP-bound open state of the receptors. Moreover, weakening or strengthening these physical interactions with engineered intersubunit metal bridges remarkably decreased or increased the open probability of the receptors, respectively. Further disulfide cross-linking and covalent modification confirmed that the intersubunit physical couplings among the DF and two lower body domains fostered by the LF domain at the open state act as an integrated structural element that is stringently required for the channel gating of P2X4 receptors. Our observations provide new mechanistic insights into P2X receptor activation and will stimulate development of new allosteric modulators of P2X receptors.

Indexed as

Molecular Dynamics SimulationHEK293 CellsHumansIon Channel GatingProtein DomainsReceptors, Purinergic P2X4Receptors, Purinergic P2X4conformational changegatingion channelmolecular simulationsP2X receptorsphysical couplingsprotein domainreceptor structure-functionsingle channel recording

Identifiers

PMID28302727
PMCPMC5418059

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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.