中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Different conformational responses of the beta(2)-adrenergic receptor-Gs complex upon binding of the partial agonist salbutamol or the full agonist isoprenaline

文献类型:期刊论文

作者Yang, Fan1,2; Ling, Shenglong1,2; Zhou, Yingxin1,2; Zhang, Yanan1,2; Lv, Pei1,2; Liu, Sanling1,2; Fang, Wei1,2; Sun, Wenjing1,2; Hu, Liaoyuan A.3; Zhang, Longhua1,2
刊名NATIONAL SCIENCE REVIEW
出版日期2021-09-01
卷号8
关键词cryo-EM structure G protein-coupled receptor (GPCR) partial and full agonists conformational change desensitization
ISSN号2095-5138
DOI10.1093/nsr/nwaa284
通讯作者Shi, Pan(shipan@ustc.edu.cn) ; Tian, Changlin(cltian@ustc.edu.cn)
英文摘要G protein-coupled receptors (GPCRs) are responsible for most cytoplasmic signaling in response to extracellular ligands with different efficacy profiles. Various spectroscopic techniques have identified that agonists exhibiting varying efficacies can selectively stabilize a specific conformation of the receptor. However, the structural basis for activation of the GPCR-G protein complex by ligands with different efficacies is incompletely understood. To better understand the structural basis underlying the mechanisms by which ligands with varying efficacies differentially regulate the conformations of receptors and G proteins, we determined the structures of beta(2)AR-G alpha(s)beta gamma bound with partial agonist salbutamol or bound with full agonist isoprenaline using single-particle cryo-electron microscopy at resolutions of 3.26 angstrom and 3.80 angstrom, respectively. Structural comparisons between the beta(2)AR-Gs-salbutamol and beta(2)AR-Gs-isoprenaline complexes demonstrated that the decreased binding affinity and efficacy of salbutamol compared with those of isoprenaline might be attributed to weakened hydrogen bonding interactions, attenuated hydrophobic interactions in the orthosteric binding pocket and different conformational changes in the rotamer toggle switch in TM6. Moreover, the observed stronger interactions between the intracellular loop 2 or 3 (ICL2 or ICL3) of beta(2)AR and G alpha(s) with binding of salbutamol versus isoprenaline might decrease phosphorylation in the salbutamol-activated beta(2)AR-Gs complex. From the observed structural differences between these complexes of beta(2)AR, a mechanism of beta(2)AR activation by partial and full agonists is proposed to provide structural insights into beta(2)AR desensitization.
WOS关键词PROTEIN-COUPLED RECEPTOR ; STRUCTURAL INSIGHTS ; CRYSTAL-STRUCTURE ; BETA(2) ; PHOSPHORYLATION ; EFFICACY ; BIAS
资助项目National Key Research and Development Project of China[2016YFA0400903] ; National Key Research and Development Project of China[2017YFA0505400] ; National Natural Science Foundation of China[21825703] ; National Natural Science Foundation of China[31971152] ; Innovative Program of Development Foundation of Hefei Center for Physical Science and Technology[2018CXFX004] ; Amgen Postdoc Fellowship (China)
WOS研究方向Science & Technology - Other Topics
语种英语
WOS记录号WOS:000701659300006
出版者OXFORD UNIV PRESS
资助机构National Key Research and Development Project of China ; National Natural Science Foundation of China ; Innovative Program of Development Foundation of Hefei Center for Physical Science and Technology ; Amgen Postdoc Fellowship (China)
源URL[http://ir.hfcas.ac.cn:8080/handle/334002/124897]  
专题中国科学院合肥物质科学研究院
通讯作者Shi, Pan; Tian, Changlin
作者单位1.Univ Sci & Technol China, Hefei Natl Lab Phys Sci Microscale, Hefei 230026, Peoples R China
2.Univ Sci & Technol China, Sch Life Sci, Hefei 230026, Peoples R China
3.Amgen Res, Amgen Asia R&D Ctr, Shanghai 201210, Peoples R China
4.Chinese Acad Sci, High Magnet Field Lab, Hefei 230030, Peoples R China
推荐引用方式
GB/T 7714
Yang, Fan,Ling, Shenglong,Zhou, Yingxin,et al. Different conformational responses of the beta(2)-adrenergic receptor-Gs complex upon binding of the partial agonist salbutamol or the full agonist isoprenaline[J]. NATIONAL SCIENCE REVIEW,2021,8.
APA Yang, Fan.,Ling, Shenglong.,Zhou, Yingxin.,Zhang, Yanan.,Lv, Pei.,...&Tian, Changlin.(2021).Different conformational responses of the beta(2)-adrenergic receptor-Gs complex upon binding of the partial agonist salbutamol or the full agonist isoprenaline.NATIONAL SCIENCE REVIEW,8.
MLA Yang, Fan,et al."Different conformational responses of the beta(2)-adrenergic receptor-Gs complex upon binding of the partial agonist salbutamol or the full agonist isoprenaline".NATIONAL SCIENCE REVIEW 8(2021).

入库方式: OAI收割

来源:合肥物质科学研究院

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