中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Solvent-accessibility of discrete residue positions in the polypeptide hormone glucagon by F-19-NMR observation of 4-fluorophenylalanine

文献类型:期刊论文

作者Hou, Yaguang2,3,4,7; Hu, Wanhui2; Li, Xiaona5; Skinner, John J.2; Liu, Dongsheng2; Wuthrich, Kurt1,2,6
刊名JOURNAL OF BIOMOLECULAR NMR
出版日期2017-05
卷号68期号:1页码:1-6
关键词F-19-NMR Glucagon F-19 chemical shift Solvent exposure from D2O effects
ISSN号0925-2738
DOI10.1007/s10858-017-0107-8
文献子类Article
英文摘要The amino acid 4-fluoro-l-phenylalanine (4F-Phe) was introduced at the positions of Phe6 and Phe22 in the 29-residue polypeptide hormone glucagon by expressing glucagon in E. coli in the presence of an excess of 4F-Phe. Glucagon regulates blood glucose homeostasis by interaction with the glucagon receptor (GCGR), a class B GPCR. By referencing to the 4F-Phe chemical shifts at varying D2O concentrations, the solvent exposure of the two Phe sites along the glucagon sequence was determined, showing that 4F-Phe6 was fully solvent exposed and 4F-Phe22 was only partially exposed. The incorporation of fluorine atoms in polypeptide hormones paves the way for novel studies of their interactions with membrane-spanning receptors, specifically by differentiating between effects on the solvent accessibility, the line shapes, and the chemical shifts from interactions with lipids, detergents and proteins. Studies of interactions of GCGR with ligands in solution is at this point of keen interest, given that recent crystallographic studies revealed that an apparent small molecule antagonist actually binds as an allosteric effector at a distance of similar to 20 from the orthosteric ligand binding site (Jazayeri et al., in Nature 533:274-277, 2016).
WOS关键词PROTEIN-COUPLED RECEPTOR ; CRYSTAL-STRUCTURE ; NMR ; ANTAGONIST ; RESONANCE ; GPCRS ; SITE
资助项目ShanghaiTech University[00000000] ; Shanghai Municipal Government[00000000] ; Hefei Science Center[2015HSC-UE012] ; National Natural Science Foundation of China[31670733] ; Shanghai 1000-talents award[00000000]
WOS研究方向Biochemistry & Molecular Biology ; Spectroscopy
语种英语
WOS记录号WOS:000403406900001
出版者SPRINGER
源URL[http://119.78.100.183/handle/2S10ELR8/272679]  
专题新药研究国家重点实验室
中科院受体结构与功能重点实验室
通讯作者Wuthrich, Kurt
作者单位1.Scripps Res Inst, Skaggs Inst Chem Biol, La Jolla, CA 92037 USA;
2.ShanghaiTech Univ, iHuman Inst, 393 Middle Huaxia Rd, Shanghai 201210, Peoples R China;
3.Chinese Acad Sci, Shanghai Inst Biol Sci, Inst Biochem & Cell Biol, 320 Yue Yang Rd, Shanghai 200031, Peoples R China;
4.Univ Chinese Acad Sci, Beijing 100049, Peoples R China;
5.Chinese Acad Sci, Shanghai Inst Mat Med, State Key Lab Drug Res, Shanghai 201203, Peoples R China;
6.Scripps Res Inst, Dept Integrat Struct & Computat Biol, La Jolla, CA 92037 USA;
7.ShanghaiTech Univ, Sch Life Sci & Technol, 393 Middle Huaxia Rd, Shanghai 201210, Peoples R China
推荐引用方式
GB/T 7714
Hou, Yaguang,Hu, Wanhui,Li, Xiaona,et al. Solvent-accessibility of discrete residue positions in the polypeptide hormone glucagon by F-19-NMR observation of 4-fluorophenylalanine[J]. JOURNAL OF BIOMOLECULAR NMR,2017,68(1):1-6.
APA Hou, Yaguang,Hu, Wanhui,Li, Xiaona,Skinner, John J.,Liu, Dongsheng,&Wuthrich, Kurt.(2017).Solvent-accessibility of discrete residue positions in the polypeptide hormone glucagon by F-19-NMR observation of 4-fluorophenylalanine.JOURNAL OF BIOMOLECULAR NMR,68(1),1-6.
MLA Hou, Yaguang,et al."Solvent-accessibility of discrete residue positions in the polypeptide hormone glucagon by F-19-NMR observation of 4-fluorophenylalanine".JOURNAL OF BIOMOLECULAR NMR 68.1(2017):1-6.

入库方式: OAI收割

来源:上海药物研究所

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