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X-ray laser diffraction for structure determination of the rhodopsin-arrestin complex | |
Zhou, X. Edward1; Gao, Xiang1; Barty, Anton2; Kang, Yanyong1; He, Yuanzheng1; Liu, Wei3,4; Ishchenko, Andrii5; White, Thomas A.2; Yefanov, Oleksandr2; Han, Gye Won5,6; Xu, Qingping7; de Waal, Parker W.1; Suino-Powell, Kelly M.1; Boutet, Sebastien8; Williams, Garth J.8; Wang, Meitian9; Li, Dianfan10,11; Caffrey, Martin10,11; Chapman, Henry N.2,12; Spence, John C. H.2,13; Fromme, Petra2; Weierstall, Uwe2,13; Stevens, Raymond C.5,6,14 ![]() | |
2016-04-12 | |
发表期刊 | SCIENTIFIC DATA (IF:5.8[JCR-2023],8.9[5-Year]) |
ISSN | 2052-4463 |
卷号 | 3 |
发表状态 | 已发表 |
DOI | 10.1038/sdata.2016.21 |
摘要 | Serial femtosecond X-ray crystallography (SFX) using an X-ray free electron laser (XFEL) is a recent advancement in structural biology for solving crystal structures of challenging membrane proteins, including G-protein coupled receptors (GPCRs), which often only produce microcrystals. An XFEL delivers highly intense X-ray pulses of femtosecond duration short enough to enable the collection of single diffraction images before significant radiation damage to crystals sets in. Here we report the deposition of the XFEL data and provide further details on crystallization, XFEL data collection and analysis, structure determination, and the validation of the structural model. The rhodopsin-arrestin crystal structure solved with SFX represents the first near-atomic resolution structure of a GPCR-arrestin complex, provides structural insights into understanding of arrestin-mediated GPCR signaling, and demonstrates the great potential of this SFX-XFEL technology for accelerating crystal structure determination of challenging proteins and protein complexes. |
收录类别 | SCI |
语种 | 英语 |
资助项目 | BMBF project[FKZ 05K12CH1] |
WOS研究方向 | Science & Technology - Other Topics |
WOS类目 | Multidisciplinary Sciences |
WOS记录号 | WOS:000390214400001 |
出版者 | NATURE PUBLISHING GROUP |
WOS关键词 | SERIAL FEMTOSECOND CRYSTALLOGRAPHY ; LIPIDIC CUBIC PHASE ; INDEXING AMBIGUITY ; CRYSTAL-STRUCTURE ; SPACE-GROUP ; INTEGRATION ; QUALITY |
原始文献类型 | Article ; Data Paper |
引用统计 | 正在获取...
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文献类型 | 期刊论文 |
条目标识符 | https://kms.shanghaitech.edu.cn/handle/2MSLDSTB/1869 |
专题 | iHuman研究所_特聘教授组_Raymond Stevens组 iHuman研究所 |
通讯作者 | Zhou, X. Edward; Xu, H. Eric |
作者单位 | 1.Van Andel Res Inst, Ctr Struct Biol & Drug Discovery, Lab Struct Sci, Grand Rapids, MI 49503 USA 2.Deutsch Elektronen Synchrotron DESY, Ctr Free Electron Laser Sci, D-22607 Hamburg, Germany 3.Arizona State Univ, Sch Mol Sci, Tempe, AZ 85287 USA 4.Arizona State Univ, Ctr Appl Struct Discovery, Biodesign Inst, Tempe, AZ 85287 USA 5.Univ Southern Calif, Bridge Inst, Dept Chem, Los Angeles, CA 90089 USA 6.Univ Southern Calif, Bridge Inst, Dept Biol Sci, Los Angeles, CA 90089 USA 7.SLAC Natl Accelerator Lab, Stanford Synchrotron Radiat Lightsource, Joint Ctr Struct Genom, Menlo Pk, CA 94025 USA 8.SLAC Natl Accelerator Lab, Linac Coherent Light Source LCLS, Menlo Pk, CA 94025 USA 9.Paul Scherrer Inst, Swiss Light Source, CH-5232 Villigen, Switzerland 10.Trinity Coll Dublin, Sch Med, Dublin D02 R590, Ireland 11.Trinity Coll Dublin, Sch Biochem & Immunol, Dublin D02 R590, Ireland 12.Ctr Ultrafast Imaging, D-22761 Hamburg, Germany 13.Arizona State Univ, Dept Phys, Tempe, AZ 85287 USA 14.Shanghai Tech Univ, IHuman Inst, 2F Bldg 6,99 Haike Rd, Shanghai 201210, Peoples R China 15.Chinese Acad Sci, Shanghai Inst Mat Med, Key Lab Receptor Res, Ctr Struct & Funct Drug Targets,VARI SIMM Ctr, Shanghai 201203, Peoples R China |
推荐引用方式 GB/T 7714 | Zhou, X. Edward,Gao, Xiang,Barty, Anton,et al. X-ray laser diffraction for structure determination of the rhodopsin-arrestin complex[J]. SCIENTIFIC DATA,2016,3. |
APA | Zhou, X. Edward.,Gao, Xiang.,Barty, Anton.,Kang, Yanyong.,He, Yuanzheng.,...&Xu, H. Eric.(2016).X-ray laser diffraction for structure determination of the rhodopsin-arrestin complex.SCIENTIFIC DATA,3. |
MLA | Zhou, X. Edward,et al."X-ray laser diffraction for structure determination of the rhodopsin-arrestin complex".SCIENTIFIC DATA 3(2016). |
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