Suppr超能文献

G 蛋白偶联受体的连续飞秒晶体学。

Serial Femtosecond Crystallography of G Protein-Coupled Receptors.

机构信息

Department of Chemistry and Bridge Institute, University of Southern California, Los Angeles, California 90089, USA; email:

出版信息

Annu Rev Biophys. 2018 May 20;47:377-397. doi: 10.1146/annurev-biophys-070317-033239. Epub 2018 Mar 15.

Abstract

G protein-coupled receptors (GPCRs) represent a large superfamily of membrane proteins that mediate cell signaling and regulate a variety of physiological processes in the human body. Structure-function studies of this superfamily were enabled a decade ago by multiple breakthroughs in technology that included receptor stabilization, crystallization in a membrane environment, and microcrystallography. The recent emergence of X-ray free-electron lasers (XFELs) has further accelerated structural studies of GPCRs and other challenging proteins by overcoming radiation damage and providing access to high-resolution structures and dynamics using micrometer-sized crystals. Here, we summarize key technology advancements and major milestones of GPCR research using XFELs and provide a brief outlook on future developments in the field.

摘要

G 蛋白偶联受体 (GPCRs) 是一大类膜蛋白超家族,介导细胞信号转导,调节人体多种生理过程。该超家族的结构-功能研究得益于十年前多项技术突破,包括受体稳定化、在膜环境中结晶和微晶体学。最近 X 射线自由电子激光 (XFEL) 的出现通过克服辐射损伤并使用微米级晶体提供了获取高分辨率结构和动态信息的途径,进一步加速了 GPCR 和其他具有挑战性的蛋白质的结构研究。本文总结了使用 XFEL 进行 GPCR 研究的关键技术进展和主要里程碑,并对该领域的未来发展进行了简要展望。

相似文献

1
Serial Femtosecond Crystallography of G Protein-Coupled Receptors.
Annu Rev Biophys. 2018 May 20;47:377-397. doi: 10.1146/annurev-biophys-070317-033239. Epub 2018 Mar 15.
2
Serial femtosecond crystallography of G protein-coupled receptors.
Science. 2013 Dec 20;342(6165):1521-4. doi: 10.1126/science.1244142.
3
Serial Femtosecond Crystallography of Membrane Proteins.
Adv Exp Med Biol. 2016;922:151-160. doi: 10.1007/978-3-319-35072-1_11.
4
An outlook on using serial femtosecond crystallography in drug discovery.
Expert Opin Drug Discov. 2019 Sep;14(9):933-945. doi: 10.1080/17460441.2019.1626822. Epub 2019 Jun 11.
5
Femtosecond crystallography of membrane proteins in the lipidic cubic phase.
Philos Trans R Soc Lond B Biol Sci. 2014 Jul 17;369(1647):20130314. doi: 10.1098/rstb.2013.0314.
6
A Bright Future for Serial Femtosecond Crystallography with XFELs.
Trends Biochem Sci. 2017 Sep;42(9):749-762. doi: 10.1016/j.tibs.2017.06.007. Epub 2017 Jul 18.
8
Structural biology of G protein-coupled receptors: new opportunities from XFELs and cryoEM.
Curr Opin Struct Biol. 2018 Aug;51:44-52. doi: 10.1016/j.sbi.2018.03.009. Epub 2018 Mar 16.
10
Serial Crystallography for Structure-Based Drug Discovery.
Trends Pharmacol Sci. 2020 Nov;41(11):830-839. doi: 10.1016/j.tips.2020.08.009. Epub 2020 Sep 16.

引用本文的文献

1
Progress in structure-based drug development targeting chemokine receptors.
Front Pharmacol. 2025 Jun 9;16:1603950. doi: 10.3389/fphar.2025.1603950. eCollection 2025.
3
Uncovering the unique characteristics of different groups of 5-HTR ligands with reference to their interaction with the target protein.
Pharmacol Rep. 2024 Oct;76(5):1130-1146. doi: 10.1007/s43440-024-00622-4. Epub 2024 Jul 6.
4
The time revolution in macromolecular crystallography.
Struct Dyn. 2024 Apr 12;11(2):020901. doi: 10.1063/4.0000247. eCollection 2024 Mar.
6
Review of serial femtosecond crystallography including the COVID-19 pandemic impact and future outlook.
Structure. 2023 Nov 2;31(11):1306-1319. doi: 10.1016/j.str.2023.10.005. Epub 2023 Oct 27.
7
Emerging Time-Resolved X-Ray Diffraction Approaches for Protein Dynamics.
Annu Rev Biophys. 2023 May 9;52:255-274. doi: 10.1146/annurev-biophys-111622-091155.
8
Serial femtosecond crystallography.
Nat Rev Methods Primers. 2022 Aug 4;2. doi: 10.1038/s43586-022-00141-7.
9
Determining biomolecular structures near room temperature using X-ray crystallography: concepts, methods and future optimization.
Acta Crystallogr D Struct Biol. 2023 Jan 1;79(Pt 1):78-94. doi: 10.1107/S2059798322011652.
10
Electrically stimulated droplet injector for reduced sample consumption in serial crystallography.
Biophys Rep (N Y). 2022 Sep 29;2(4):100081. doi: 10.1016/j.bpr.2022.100081. eCollection 2022 Dec 14.

本文引用的文献

1
Chemically Stable Lipids for Membrane Protein Crystallization.
Cryst Growth Des. 2017 Jun 7;17(6):3502-3511. doi: 10.1021/acs.cgd.7b00458. Epub 2017 May 12.
2
Identification of Phosphorylation Codes for Arrestin Recruitment by G Protein-Coupled Receptors.
Cell. 2017 Jul 27;170(3):457-469.e13. doi: 10.1016/j.cell.2017.07.002.
3
A Bright Future for Serial Femtosecond Crystallography with XFELs.
Trends Biochem Sci. 2017 Sep;42(9):749-762. doi: 10.1016/j.tibs.2017.06.007. Epub 2017 Jul 18.
4
Structural insights into the extracellular recognition of the human serotonin 2B receptor by an antibody.
Proc Natl Acad Sci U S A. 2017 Aug 1;114(31):8223-8228. doi: 10.1073/pnas.1700891114. Epub 2017 Jul 17.
5
Time-Resolved Macromolecular Crystallography at Modern X-Ray Sources.
Methods Mol Biol. 2017;1607:273-294. doi: 10.1007/978-1-4939-7000-1_11.
6
Structure of the full-length glucagon class B G-protein-coupled receptor.
Nature. 2017 Jun 8;546(7657):259-264. doi: 10.1038/nature22363. Epub 2017 May 17.
8
Structural basis for selectivity and diversity in angiotensin II receptors.
Nature. 2017 Apr 20;544(7650):327-332. doi: 10.1038/nature22035. Epub 2017 Apr 5.
9
Structural enzymology using X-ray free electron lasers.
Struct Dyn. 2016 Dec 15;4(4):044003. doi: 10.1063/1.4972069. eCollection 2017 Jul.
10
A three-dimensional movie of structural changes in bacteriorhodopsin.
Science. 2016 Dec 23;354(6319):1552-1557. doi: 10.1126/science.aah3497.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验