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Molecular Biophysics
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High-throughput screen, using time-resolved FRET, yields actin-binding compounds that modulate actin–myosin structure and function
Journal of Biological ChemistryVol. 293Issue 31p12288–12298Published online: June 4, 2018- Piyali Guhathakurta
- Ewa Prochniewicz
- Benjamin D. Grant
- Kurt C. Peterson
- David D. Thomas
Cited in Scopus: 17We have used a novel time-resolved FRET (TR-FRET) assay to detect small-molecule modulators of actin–myosin structure and function. Actin–myosin interactions play crucial roles in the generation of cellular force and movement. Numerous mutations and post-translational modifications of actin or myosin disrupt muscle function and cause life-threatening syndromes. Here, we used a FRET biosensor to identify modulators that bind to the actin–myosin interface and alter the structural dynamics of this complex.