1.Diverse GPCRs exhibit conserved water networks for stabilization and activation

作　　者：A. J. Venkatakrishnan ;A. J. Venkatakrishnan ;Anthony K. Ma 等

出　　处：Proceedings of the National Academy of Sciences. 2019 ;116(8):3288-3293.doi:10.1073/pnas.1809251116

出版社：The National Academy of Sciences of the United States of America

文章 ID：226777158

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2.Tandem malonate-based glucosides (TMGs) for membrane protein structural studies

作　　者：Hazrat Hussain ;Jonas S. Mortensen ;Yang Du 等

出　　处：Scientific Reports. 2017 ;7(1).doi:10.1038/s41598-017-03809-3

出版社：Springer Nature

文章 ID：235887382

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3.Structure-based discovery of β2-adrenergic receptor ligands

作　　者：Peter Kolb ;Daniel M. Rosenbaum ;John J. Irwin 等

出　　处：Proceedings of the National Academy of Sciences. 2009 ;106(16):6843-6848.doi:10.1073/pnas.0812657106

出版社：The National Academy of Sciences of the United States of America

文章 ID：200591460

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4.Agonist-induced conformational changes in the G-protein-coupling domain of the β2 adrenergic receptor

作　　者：Pejman Ghanouni ;Jacqueline J. Steenhuis ;David L. Farrens 等

出　　处：Proceedings of the National Academy of Sciences. 2001 ;98(11):5997-6002.doi:10.1073/pnas.101126198

出版社：The National Academy of Sciences of the United States of America

文章 ID：200557349

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5.Single-molecule spectroscopy of the β2 adrenergic receptor: Observation of conformational substates in a membrane protein

作　　者：Gadi Peleg ;Pejman Ghanouni ;Brian K. Kobilka 等

出　　处：Proceedings of the National Academy of Sciences. 2001 ;98(15):8469-8474.doi:10.1073/pnas.151239698

出版社：The National Academy of Sciences of the United States of America

文章 ID：200557750

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6.Crystal structure of the adenosine A2A receptor bound to an antagonist reveals a potential allosteric pocket

作　　者：Bingfa Sun ;Priti Bachhawat ;Matthew Ling-Hon Chu 等

出　　处：Proceedings of the National Academy of Sciences. 2017 ;114(8):2066-2071.doi:10.1073/pnas.1621423114

出版社：The National Academy of Sciences of the United States of America

文章 ID：191705697

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7.Structure-guided development of selective M3 muscarinic acetylcholine receptor antagonists

作　　者：Hongtao Liu ;Josefa Hofmann ;Inbar Fish 等

出　　处：Proceedings of the National Academy of Sciences. 2018 ;115(47):12046-12050.doi:10.1073/pnas.1813988115

出版社：The National Academy of Sciences of the United States of America

文章 ID：222235197

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8.Structure-based discovery of selective positive allosteric modulators of antagonists for the M2 muscarinic acetylcholine receptor

作　　者：Magdalena Korczynska ;Mary J. Clark ;Celine Valant 等

出　　处：Proceedings of the National Academy of Sciences. 2018 ;115(10):E2419-E2428.doi:10.1073/pnas.1718037115

出版社：The National Academy of Sciences of the United States of America

文章 ID：213273375

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9.Structural basis for GLP-1 receptor activation by LY3502970, an orally active nonpeptide agonist

作　　者：Takahiro Kawai ;Bingfa Sun ;Hitoshi Yoshino 等

出　　处：Proceedings of the National Academy of Sciences. 2020 ;117(47):29959-29967.doi:10.1073/pnas.2014879117

出版社：The National Academy of Sciences of the United States of America

文章 ID：260993951

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10.Analysis of β2AR-Gs and β2AR-Gi complex formation by NMR spectroscopy

作　　者：Xiuyan Ma ;Yunfei Hu ;Hossein Batebi 等

出　　处：Proceedings of the National Academy of Sciences. 2020 ;117(37):23096-23105.doi:10.1073/pnas.2009786117

出版社：The National Academy of Sciences of the United States of America

文章 ID：260994822

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