Evidence map›Paper›PMID 27085723›Full record

ArticleProtein & cell2016

In vitro expression and analysis of the 826 human G protein-coupled receptors.

Xuechen Lv, Junlin Liu, Qiaoyun Shi, Qiwen Tan, Dong Wu, John J Skinner, Angela L Walker, Lixia Zhao, Xiangxiang Gu, Na Chen and 7 more

Open access · diamondAbstract read
In one paragraph

Article in Protein & cell, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

35 citing papers in PubMed, 73 citations in OpenAlex.

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  13. MUG: A mutation overview of GPCR subfamily A17 receptors.Computational and structural biotechnology journal · 2023
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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

17 authors at 2 institutions in 2 countries.

Xuechen LviHuman Institute, ShanghaiTech University, Shanghai, 201210, China.
Junlin LiuiHuman Institute, ShanghaiTech University, Shanghai, 201210, China.
Qiaoyun ShiiHuman Institute, ShanghaiTech University, Shanghai, 201210, China.
Qiwen TaniHuman Institute, ShanghaiTech University, Shanghai, 201210, China.
Dong WuiHuman Institute, ShanghaiTech University, Shanghai, 201210, China.
John J SkinneriHuman Institute, ShanghaiTech University, Shanghai, 201210, China.
Angela L WalkerDepartment of Biological Sciences, Bridge Institute, University of Southern California, Los Angeles, CA, 90089, USA.
Lixia ZhaoiHuman Institute, ShanghaiTech University, Shanghai, 201210, China.
Xiangxiang GuiHuman Institute, ShanghaiTech University, Shanghai, 201210, China.
Na CheniHuman Institute, ShanghaiTech University, Shanghai, 201210, China.
Lu XueiHuman Institute, ShanghaiTech University, Shanghai, 201210, China.
Pei SiiHuman Institute, ShanghaiTech University, Shanghai, 201210, China.
Lu ZhangiHuman Institute, ShanghaiTech University, Shanghai, 201210, China.
Zeshi WangiHuman Institute, ShanghaiTech University, Shanghai, 201210, China.
Vsevolod KatritchDepartment of Biological Sciences, Bridge Institute, University of Southern California, Los Angeles, CA, 90089, USA.
Zhi-Jie LiuiHuman Institute, ShanghaiTech University, Shanghai, 201210, China.
Raymond C StevensiHuman Institute, ShanghaiTech University, Shanghai, 201210, China. stevens@shanghaitech.edu.cn.
ShanghaiTech University · CNUniversity of Southern California · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

G protein-coupled receptors (GPCRs) are involved in all human physiological systems where they are responsible for transducing extracellular signals into cells. GPCRs signal in response to a diverse array of stimuli including light, hormones, and lipids, where these signals affect downstream cascades to impact both health and disease states. Yet, despite their importance as therapeutic targets, detailed molecular structures of only 30 GPCRs have been determined to date. A key challenge to their structure determination is adequate protein expression. Here we report the quantification of protein expression in an insect cell expression system for all 826 human GPCRs using two different fusion constructs. Expression characteristics are analyzed in aggregate and among each of the five distinct subfamilies. These data can be used to identify trends related to GPCR expression between different fusion constructs and between different GPCR families, and to prioritize lead candidates for future structure determination feasibility.

Indexed as

AnimalsComputational BiologyCrystallography, X-RayGene ExpressionHumansPlasmidsProtein DomainsReceptors, Adrenergic, beta-1Receptors, G-Protein-CoupledReceptors, OdorantReceptors, Purinergic P1Sf9 CellsSpodopteraReceptors, Adrenergic, beta-1Receptors, G-Protein-CoupledReceptors, OdorantReceptors, Purinergic P1fusion constructG protein-coupled receptorsinsectprotein expressionsurface expression analysis

Identifiers

PMID27085723
PMCPMC4853319
OpenAlexW2340722299

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.