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826种人类G蛋白偶联受体的体外表达与分析

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

作者信息

Lv Xuechen, Liu Junlin, Shi Qiaoyun, Tan Qiwen, Wu Dong, Skinner John J, Walker Angela L, Zhao Lixia, Gu Xiangxiang, Chen Na, Xue Lu, Si Pei, Zhang Lu, Wang Zeshi, Katritch Vsevolod, Liu Zhi-Jie, Stevens Raymond C

机构信息

iHuman Institute, ShanghaiTech University, Shanghai, 201210, China.

Department of Biological Sciences, Bridge Institute, University of Southern California, Los Angeles, CA, 90089, USA.

出版信息

Protein Cell. 2016 May;7(5):325-37. doi: 10.1007/s13238-016-0263-8. Epub 2016 Apr 16.

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.

摘要

G蛋白偶联受体(GPCRs)参与人体所有生理系统,负责将细胞外信号转导至细胞内。GPCRs对包括光、激素和脂质在内的多种刺激作出信号响应,这些信号影响下游级联反应,进而影响健康和疾病状态。然而,尽管它们作为治疗靶点很重要,但迄今为止仅确定了30种GPCRs的详细分子结构。其结构确定的一个关键挑战是足够的蛋白质表达。在此,我们报告了使用两种不同的融合构建体对昆虫细胞表达系统中所有826种人类GPCRs的蛋白质表达进行定量。对表达特征进行了总体分析以及在五个不同亚家族中的每个亚家族内进行分析。这些数据可用于识别不同融合构建体之间以及不同GPCR家族之间与GPCR表达相关的趋势,并为未来结构确定的可行性确定潜在候选物的优先级。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/56c6/4853319/f19f3d8e5509/13238_2016_263_Fig1_HTML.jpg

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