Evidence map›Paper›PMID 36984688›Full record

ArticleMembranes2023

Cholesterol in Class C GPCRs: Role, Relevance, and Localization.

Ugochi H Isu, Shadi A Badiee, Ehsaneh Khodadadi, Mahmoud Moradi

Open access · goldAbstract read
In one paragraph

Article in Membranes, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

15 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
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  12. Molecular regulation of calcium-sensing receptor (CaSR)-mediated signaling.Chronic diseases and translational medicine · 2024
    Review
  13. Article
  14. Article
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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

4 authors at 1 institution in 1 country.

Ugochi H IsuDepartment of Chemistry and Biochemistry, University of Arkansas, Fayetteville, AR 72701, USA.
Shadi A BadieeDepartment of Chemistry and Biochemistry, University of Arkansas, Fayetteville, AR 72701, USA.ORCID 0000-0002-1037-6226
Ehsaneh KhodadadiDepartment of Chemistry and Biochemistry, University of Arkansas, Fayetteville, AR 72701, USA.
Mahmoud MoradiDepartment of Chemistry and Biochemistry, University of Arkansas, Fayetteville, AR 72701, USA.ORCID 0000-0002-0601-402X
University of Arkansas at Fayetteville · US

Funding

Physics-based characterization of functionally relevant protein conformational dynamicsR35GM147423 · NIGMS · UNIVERSITY OF ARKANSAS AT FAYETTEVILLE · PI Mahmoud Moradi · 2022 to 2026
$1.7M
NIGMS NIH HHS R35 GM147423NIH HHS R35GM147423
6 · The paper itself

Abstract

G-protein coupled receptors (GPCRs), one of the largest superfamilies of cell-surface receptors, are heptahelical integral membrane proteins that play critical roles in virtually every organ system. G-protein-coupled receptors operate in membranes rich in cholesterol, with an imbalance in cholesterol level within the vicinity of GPCR transmembrane domains affecting the structure and/or function of many GPCRs, a phenomenon that has been linked to several diseases. These effects of cholesterol could result in indirect changes by altering the mechanical properties of the lipid environment or direct changes by binding to specific sites on the protein. There are a number of studies and reviews on how cholesterol modulates class A GPCRs; however, this area of study is yet to be explored for class C GPCRs, which are characterized by a large extracellular region and often form constitutive dimers. This review highlights specific sites of interaction, functions, and structural dynamics involved in the cholesterol recognition of the class C GPCRs. We summarize recent data from some typical family members to explain the effects of membrane cholesterol on the structural features and functions of class C GPCRs and speculate on their corresponding therapeutic potential.

Indexed as

cholesterolclass C GPCRsGPCRsG-protein-coupled-receptorsmembrane proteinprotein–lipid interactionssterols

Identifiers

PMID36984688
PMCPMC10056374
OpenAlexW4323314508

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.