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整体膜蛋白动力学和功能的单分子成像

Single-Molecule Imaging of Integral Membrane Protein Dynamics and Function.

机构信息

Department of Structural Biology, St. Jude Children's Research Hospital, Memphis, Tennessee, USA; email:

Department of Chemical Biology & Therapeutics, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.

出版信息

Annu Rev Biophys. 2024 Jul;53(1):427-453. doi: 10.1146/annurev-biophys-070323-024308.

Abstract

Integral membrane proteins (IMPs) play central roles in cellular physiology and represent the majority of known drug targets. Single-molecule fluorescence and fluorescence resonance energy transfer (FRET) methods have recently emerged as valuable tools for investigating structure-function relationships in IMPs. This review focuses on the practical foundations required for examining polytopic IMP function using single-molecule FRET (smFRET) and provides an overview of the technical and conceptual frameworks emerging from this area of investigation. In this context, we highlight the utility of smFRET methods to reveal transient conformational states critical to IMP function and the use of smFRET data to guide structural and drug mechanism-of-action investigations. We also identify frontiers where progress is likely to be paramount to advancing the field.

摘要

整合膜蛋白(IMPs)在细胞生理学中发挥着核心作用,并且是大多数已知药物靶点的代表。单分子荧光和荧光共振能量转移(FRET)方法最近已成为研究 IMP 结构-功能关系的有价值的工具。本综述重点介绍了使用单分子 FRET(smFRET)研究多跨膜 IMP 功能所需的实用基础,并概述了该研究领域出现的技术和概念框架。在这种情况下,我们强调了 smFRET 方法在揭示对 IMP 功能至关重要的瞬态构象状态方面的效用,以及使用 smFRET 数据来指导结构和药物作用机制的研究。我们还确定了可能对推进该领域至关重要的前沿领域。

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