费斯特共振能量转移
生物物理学
生物传感器
肽
生物
荧光
生物化学
量子力学
物理
作者
Bei Liu,Orrin J. Stone,Michael Pablo,J. Cody Herron,Ana T. Nogueira,Onur Dağliyan,Jonathan B. Grimm,Luke D. Lavis,Timothy C. Elston,Klaus M. Hahn
出处
期刊:Cell
[Cell Press]
日期:2021-10-01
卷期号:184 (22): 5670-5685.e23
被引量:22
标识
DOI:10.1016/j.cell.2021.09.026
摘要
We describe an approach to study the conformation of individual proteins during single particle tracking (SPT) in living cells. "Binder/tag" is based on incorporation of a 7-mer peptide (the tag) into a protein where its solvent exposure is controlled by protein conformation. Only upon exposure can the peptide specifically interact with a reporter protein (the binder). Thus, simple fluorescence localization reflects protein conformation. Through direct excitation of bright dyes, the trajectory and conformation of individual proteins can be followed. Simple protein engineering provides highly specific biosensors suitable for SPT and FRET. We describe tagSrc, tagFyn, tagSyk, tagFAK, and an orthogonal binder/tag pair. SPT showed slowly diffusing islands of activated Src within Src clusters and dynamics of activation in adhesions. Quantitative analysis and stochastic modeling revealed in vivo Src kinetics. The simplicity of binder/tag can provide access to diverse proteins.
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