Biosensors based on peptide exposure show single molecule conformations in live cells
Author(s) -
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
Publication year - 2021
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2021.09.026
Subject(s) - biosensor , förster resonance energy transfer , biophysics , peptide , biology , fluorescence , green fluorescent protein , biochemistry , gene , physics , quantum mechanics
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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