• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

溶液核磁共振揭示多跨螺旋膜蛋白中与功能相关的动力学

Function-Related Dynamics in Multi-Spanning Helical Membrane Proteins Revealed by Solution NMR.

作者信息

Takeuchi Koh, Kofuku Yutaka, Imai Shunsuke, Ueda Takumi, Tokunaga Yuji, Toyama Yuki, Shiraishi Yutaro, Shimada Ichio

机构信息

Cellular and Molecular Biotechnology Research Institute, National Institute of Advanced Industrial Science and Technology, Aomi, Koto, Tokyo 135-0064, Japan.

Graduate School of Pharmaceutical Sciences, The University of Tokyo, Hongo, Bunkyo, Tokyo 113-0033, Japan.

出版信息

Membranes (Basel). 2021 Aug 9;11(8):604. doi: 10.3390/membranes11080604.

DOI:10.3390/membranes11080604
PMID:34436367
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8398610/
Abstract

A primary biological function of multi-spanning membrane proteins is to transfer information and/or materials through a membrane by changing their conformations. Therefore, particular dynamics of the membrane proteins are tightly associated with their function. The semi-atomic resolution dynamics information revealed by NMR is able to discriminate function-related dynamics from random fluctuations. This review will discuss several studies in which quantitative dynamics information by solution NMR has contributed to revealing the structural basis of the function of multi-spanning membrane proteins, such as ion channels, GPCRs, and transporters.

摘要

多跨膜蛋白的一个主要生物学功能是通过改变其构象在膜上传递信息和/或物质。因此,膜蛋白的特定动力学与它们的功能紧密相关。核磁共振(NMR)揭示的半原子分辨率动力学信息能够区分与功能相关的动力学和随机波动。本综述将讨论几项研究,其中溶液核磁共振提供的定量动力学信息有助于揭示多跨膜蛋白(如离子通道、G蛋白偶联受体和转运蛋白)功能的结构基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/37ce/8398610/89a586238bb6/membranes-11-00604-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/37ce/8398610/0a14b0c15ae2/membranes-11-00604-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/37ce/8398610/6b637e6f2653/membranes-11-00604-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/37ce/8398610/89a586238bb6/membranes-11-00604-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/37ce/8398610/0a14b0c15ae2/membranes-11-00604-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/37ce/8398610/6b637e6f2653/membranes-11-00604-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/37ce/8398610/89a586238bb6/membranes-11-00604-g003.jpg

相似文献

1
Function-Related Dynamics in Multi-Spanning Helical Membrane Proteins Revealed by Solution NMR.溶液核磁共振揭示多跨螺旋膜蛋白中与功能相关的动力学
Membranes (Basel). 2021 Aug 9;11(8):604. doi: 10.3390/membranes11080604.
2
19F NMR as a versatile tool to study membrane protein structure and dynamics.19F NMR 作为一种研究膜蛋白结构和动力学的通用工具。
Biol Chem. 2019 Sep 25;400(10):1277-1288. doi: 10.1515/hsz-2018-0473.
3
Functional dynamics of cell surface membrane proteins.细胞表面膜蛋白的功能动力学
J Magn Reson. 2014 Apr;241:86-96. doi: 10.1016/j.jmr.2013.11.007. Epub 2013 Nov 22.
4
Structural fluctuations between two conformational states of a transmembrane helical peptide are related to its channel-forming properties in planar lipid membranes.跨膜螺旋肽的两种构象状态之间的结构波动与其在平面脂质膜中的通道形成特性相关。
Eur J Biochem. 1993 Mar 1;212(2):305-13. doi: 10.1111/j.1432-1033.1993.tb17663.x.
5
Oligomeric structure, dynamics, and orientation of membrane proteins from solid-state NMR.基于固态核磁共振的膜蛋白寡聚体结构、动力学及取向
Structure. 2006 Dec;14(12):1731-40. doi: 10.1016/j.str.2006.10.002.
6
Structure and Dynamics of Membrane Proteins from Solid-State NMR.固态 NMR 研究膜蛋白的结构与动力学。
Annu Rev Biophys. 2018 May 20;47:201-222. doi: 10.1146/annurev-biophys-070816-033712. Epub 2018 Mar 2.
7
Multi-scaled normal mode analysis method for dynamics simulation of protein-membrane complexes: A case study of potassium channel gating motion correlations.用于蛋白质-膜复合物动力学模拟的多尺度正常模式分析方法:以钾通道门控运动相关性为例的研究
J Chem Phys. 2015 Oct 7;143(13):134113. doi: 10.1063/1.4932329.
8
Molecular dynamics simulations of the STAS domains of rat prestin and human pendrin reveal conformational motions in conserved flexible regions.大鼠prestin和人类pendrin的STAS结构域的分子动力学模拟揭示了保守柔性区域中的构象运动。
Cell Physiol Biochem. 2014;33(3):605-20. doi: 10.1159/000358638. Epub 2014 Feb 27.
9
Solution NMR spectroscopy of GPCRs: Residue-specific labeling strategies with a focus on C-methyl methionine labeling of the atypical chemokine receptor ACKR3.G蛋白偶联受体的溶液核磁共振波谱:基于残基特异性的标记策略,重点是对非典型趋化因子受体ACKR3进行碳甲基甲硫氨酸标记
Methods Cell Biol. 2019;149:259-288. doi: 10.1016/bs.mcb.2018.09.004. Epub 2018 Nov 15.
10
Application of Solution NMR to Structural Studies on α-Helical Integral Membrane Proteins.溶液 NMR 在 α-螺旋跨膜蛋白结构研究中的应用。
Molecules. 2017 Aug 15;22(8):1347. doi: 10.3390/molecules22081347.

引用本文的文献

1
Bringing GPCR Structural Biology to Medical Applications: Insights from Both V2 Vasopressin and Mu-Opioid Receptors.将GPCR结构生物学应用于医学:来自血管加压素V2受体和μ-阿片受体的见解
Membranes (Basel). 2023 Jun 16;13(6):606. doi: 10.3390/membranes13060606.
2
Advanced Research on Structure-Function Relationships of Membrane Proteins.膜蛋白结构-功能关系的前沿研究
Membranes (Basel). 2022 Jun 29;12(7):672. doi: 10.3390/membranes12070672.

本文引用的文献

1
Allosteric drug transport mechanism of multidrug transporter AcrB.多药外排转运蛋白 AcrB 的变构药物转运机制。
Nat Commun. 2021 Jun 29;12(1):3889. doi: 10.1038/s41467-021-24151-3.
2
Structure and dynamics of the drug-bound bacterial transporter EmrE in lipid bilayers.药物结合的细菌转运蛋白 EmrE 在脂质双层中的结构和动力学。
Nat Commun. 2021 Jan 8;12(1):172. doi: 10.1038/s41467-020-20468-7.
3
Mechanism of hERG inhibition by gating-modifier toxin, APETx1, deduced by functional characterization.通过功能特征分析推断门控调节剂毒素 APETx1 抑制 hERG 的机制。
BMC Mol Cell Biol. 2021 Jan 7;22(1):3. doi: 10.1186/s12860-020-00337-3.
4
The Dynamics of the Neuropeptide Y Receptor Type 1 Investigated by Solid-State NMR and Molecular Dynamics Simulation.通过固态 NMR 和分子动力学模拟研究神经肽 Y 受体 1 的动力学。
Molecules. 2020 Nov 24;25(23):5489. doi: 10.3390/molecules25235489.
5
Structure and Dynamics of GPCRs in Lipid Membranes: Physical Principles and Experimental Approaches.G 蛋白偶联受体在脂质膜中的结构与动力学:物理原理与实验方法。
Molecules. 2020 Oct 15;25(20):4729. doi: 10.3390/molecules25204729.
6
Conformational equilibrium shift underlies altered K channel gating as revealed by NMR.构象平衡转移是通过 NMR 揭示的改变钾通道门控的基础。
Nat Commun. 2020 Oct 14;11(1):5168. doi: 10.1038/s41467-020-19005-3.
7
Structural biology of human GPCR drugs and endogenous ligands - insights from NMR spectroscopy.人源 G 蛋白偶联受体药物和内源性配体的结构生物学——来自 NMR 光谱学的见解。
Methods. 2020 Aug 1;180:79-88. doi: 10.1016/j.ymeth.2020.08.008. Epub 2020 Sep 8.
8
Dynamics of Bacteriorhodopsin in the Dark-Adapted State from Solution Nuclear Magnetic Resonance Spectroscopy.从溶液核磁共振波谱学研究黑暗适应状态下细菌视紫红质的动力学
Angew Chem Int Ed Engl. 2020 Nov 16;59(47):20965-20972. doi: 10.1002/anie.202004393. Epub 2020 Sep 7.
9
Structural Fingerprints of an Intact Monoclonal Antibody Acquired under Formulated Storage Conditions via N Direct Detection Nuclear Magnetic Resonance.通过 N 直接检测核磁共振获得的在配方储存条件下完整单克隆抗体的结构指纹图谱。
J Med Chem. 2020 May 28;63(10):5360-5366. doi: 10.1021/acs.jmedchem.0c00231. Epub 2020 May 6.
10
A high-resolution description of β-adrenergic receptor functional dynamics and allosteric coupling from backbone NMR.从骨架 NMR 获得β-肾上腺素能受体功能动力学和变构偶联的高分辨率描述。
Nat Commun. 2020 May 5;11(1):2216. doi: 10.1038/s41467-020-15864-y.