Evidence map›Paper›PMID 35566006›Full record

ReviewMolecules (Basel, Switzerland)2022

G Protein-coupled Receptor (GPCR) Reconstitution and Labeling for Solution Nuclear Magnetic Resonance (NMR) Studies of the Structural Basis of Transmembrane Signaling.

Haoyi Ge, Huixia Wang, Benxun Pan, Dandan Feng, Canyong Guo, Lingyun Yang, Dongsheng Liu, Kurt Wüthrich

Abstract readReview
In one paragraph

Review in Molecules (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

8 authors.

Haoyi GeiHuman Institute, ShanghaiTech University, Shanghai 201210, China.ORCID 0000-0003-2763-7549
Huixia WangiHuman Institute, ShanghaiTech University, Shanghai 201210, China.
Benxun PaniHuman Institute, ShanghaiTech University, Shanghai 201210, China.ORCID 0000-0001-7982-1706
Dandan FengiHuman Institute, ShanghaiTech University, Shanghai 201210, China.ORCID 0000-0002-3256-2097
Canyong GuoiHuman Institute, ShanghaiTech University, Shanghai 201210, China.
Lingyun YangiHuman Institute, ShanghaiTech University, Shanghai 201210, China.
Dongsheng LiuiHuman Institute, ShanghaiTech University, Shanghai 201210, China.
Kurt WüthrichiHuman Institute, ShanghaiTech University, Shanghai 201210, China.

Funding

National Natural Science Foundation of China 21904088National Natural Science Foundation of China 31971153
6 · The paper itself

Abstract

G protein-coupled receptors (GPCRs) are a large membrane protein family found in higher organisms, including the human body. GPCRs mediate cellular responses to diverse extracellular stimuli and thus control key physiological functions, which makes them important targets for drug design. Signaling by GPCRs is related to the structure and dynamics of these proteins, which are modulated by extrinsic ligands as well as by intracellular binding partners such as G proteins and arrestins. Here, we review some basics of using nuclear magnetic resonance (NMR) spectroscopy in solution for the characterization of GPCR conformations and intermolecular interactions that relate to transmembrane signaling.

Indexed as

Receptors, G-Protein-CoupledSignal TransductionHumansLigandsMagnetic Resonance SpectroscopyMolecular ConformationLigandsReceptors, G-Protein-Coupled19F-NMRamino-acid-specific NMR labelingG protein-coupled receptorsin-membrane chemical modificationmembrane mimeticssequence-specific NMR labelingstable-isotope labeling

Identifiers

PMID35566006
PMCPMC9101874

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.