Single-Molecule Imaging of Integral Membrane Protein Dynamics and Function

被引:1
作者
Modak, Arnab [1 ]
Kilic, Zeliha [1 ]
Chattrakun, Kanokporn [1 ]
Terry, Daniel S. [1 ]
Kalathur, Ravi C. [1 ]
Blanchard, Scott C. [1 ,2 ]
机构
[1] St Jude Childrens Res Hosp, Dept Biol Struct, Memphis, TN 38105 USA
[2] St Jude Childrens Res Hosp, Dept Chem Biol Therapeut, Memphis, TN USA
基金
美国国家卫生研究院;
关键词
single-molecule imaging; integral membrane proteins; fluorescence resonance energy transfer; genetic code expansion; metastable energy landscape; intrinsically dynamic systems; X-RAY-STRUCTURE; PHOTOSYNTHETIC REACTION-CENTER; GENETIC-CODE EXPANSION; AMINO-ACID MUTAGENESIS; CONFORMATIONAL DYNAMICS; CRYSTAL-STRUCTURE; STRUCTURAL DYNAMICS; FLUORESCENCE SPECTROSCOPY; ALTERNATING ACCESS; BACTERIAL HOMOLOG;
D O I
10.1146/annurev-biophys-070323-024308
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
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.
引用
收藏
页码:427 / 453
页数:27
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