Structural perspective of class B1 GPCR signaling
文献类型:期刊论文
作者 | Cong, Zhaotong2; Liang, Yi-Lynn3; Zhou, Qingtong2; Darbalaei, Sanaz1,4,5; Zhao, Fenghui1,5; Feng, Wenbo2; Zhao, Lihua5; Xu, H. Eric4,5; Yang, Dehua1,3,4,5; Wang, Ming-Wei1,2,3,4,5,6 |
刊名 | TRENDS IN PHARMACOLOGICAL SCIENCES |
出版日期 | 2022-04-01 |
卷号 | 43期号:4页码:321-334 |
ISSN号 | 0165-6147 |
DOI | 10.1016/j.tips.2022.01.002 |
通讯作者 | Wang, Ming-Wei(mwwang@simm.ac.cn) |
英文摘要 | Class B1 G protein-coupled receptors (GPCRs) play important roles in human physiology and disease pathology. Using cryo-electron microscopy (cryo-EM) and X-ray crystallography, the 3D structures of all 15 members of this receptor subfamily have been determined in recent years at the near-atomic level. Although they share many structural commonalities, they show distinct features in terms of ligand recognition and receptor activation. In-depth structural analyses have yielded valuable insights into the N termini of both peptide hormones and cognate receptors, the outward movement of transmembrane helix 6 (TM6), the allosteric modulation sites located in the transmembrane domain (TMD), and the constitutive signaling bias mediated by receptor splice variants. These provide new directions for the design of better therapeutic agents, thereby making these targets more druggable. |
WOS关键词 | FACTOR CRF RECEPTOR ; GLP-1 RECEPTOR ; TRANSMEMBRANE DOMAIN ; PARATHYROID-HORMONE ; SPLICE VARIANTS ; ACTIVATION ; RECOGNITION ; PEPTIDE ; ISOFORM ; BINDING |
资助项目 | National Natural Science Foundation of China[81872915] ; National Natural Science Foundation of China[82073904] ; National Natural Science Foundation of China[32071203] ; National Natural Science Foundation of China[81773792] ; National Natural Science Foundation of China[81973373] ; National Natural Science Foundation of China[21704064] ; National Science and Technology Major Project of China - Key New Drug Creation and Manufacturing Program[2018ZX09735-001] ; National Science and Technology Major Project of China - Key New Drug Creation and Manufacturing Program[2018ZX09711002-002-005] ; National Science and Technology Major Project of China - Key New Drug Creation and Manufacturing Program[2021ZD0203400] ; National Key Basic Research Program of China[2018YFA0507000] ; Ministry of Science and Technology of China[2018YFA0507002] ; Shanghai Municipal Science and Technology Commission Major Project[2019SHZDZX02] ; Strategic Priority Research Program of ChineseAcademy of Sciences[XDB37030103] ; Novo Nordisk-CAS Research Fund[NNCAS-2017-1-CC] ; Shanghai Science and Technology Development Funds[18ZR1447800] ; Shanghai Science and Technology Development Funds[18431907100] ; Young InnovatorAssociation of CAS[2018325] ; SA-SIBS Scholarship Program |
WOS研究方向 | Pharmacology & Pharmacy |
语种 | 英语 |
出版者 | ELSEVIER SCIENCE LONDON |
WOS记录号 | WOS:000776138400007 |
源URL | [http://119.78.100.183/handle/2S10ELR8/299839] |
专题 | 中国科学院上海药物研究所 |
通讯作者 | Wang, Ming-Wei |
作者单位 | 1.Chinese Acad Sci, Natl Ctr Drug Screening, Shanghai Inst Mat Med, Shanghai 201203, Peoples R China 2.Fudan Univ, Sch Basic Med Sci, Dept Pharmacol, Shanghai 200032, Peoples R China 3.Res Ctr Deepsea Bioresources, Sanya 572025, Hainan, Peoples R China 4.Univ Chinese Acad Sci, Beijing 100049, Peoples R China 5.Chinese Acad Sci, Key Lab Receptor Res, Shanghai Inst Mat Med, Shanghai 201203, Peoples R China 6.ShanghaiTech Univ, Sch Life Sci & Technol, Shanghai 201210, Peoples R China |
推荐引用方式 GB/T 7714 | Cong, Zhaotong,Liang, Yi-Lynn,Zhou, Qingtong,et al. Structural perspective of class B1 GPCR signaling[J]. TRENDS IN PHARMACOLOGICAL SCIENCES,2022,43(4):321-334. |
APA | Cong, Zhaotong.,Liang, Yi-Lynn.,Zhou, Qingtong.,Darbalaei, Sanaz.,Zhao, Fenghui.,...&Wang, Ming-Wei.(2022).Structural perspective of class B1 GPCR signaling.TRENDS IN PHARMACOLOGICAL SCIENCES,43(4),321-334. |
MLA | Cong, Zhaotong,et al."Structural perspective of class B1 GPCR signaling".TRENDS IN PHARMACOLOGICAL SCIENCES 43.4(2022):321-334. |
入库方式: OAI收割
来源:上海药物研究所
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