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Molecular Biophysics
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- Research ArticleOpen Access
Cardiac myosin-binding protein C interaction with actin is inhibited by compounds identified in a high-throughput fluorescence lifetime screen
Journal of Biological ChemistryVol. 297Issue 1100840Published online: May 27, 2021- Thomas A. Bunch
- Piyali Guhathakurta
- Victoria C. Lepak
- Andrew R. Thompson
- Rhye-Samuel Kanassatega
- Anna Wilson
- and others
Cited in Scopus: 4Cardiac myosin-binding protein C (cMyBP-C) interacts with actin and myosin to modulate cardiac muscle contractility. These interactions are disfavored by cMyBP-C phosphorylation. Heart failure patients often display decreased cMyBP-C phosphorylation, and phosphorylation in model systems has been shown to be cardioprotective against heart failure. Therefore, cMyBP-C is a potential target for heart failure drugs that mimic phosphorylation or perturb its interactions with actin/myosin. Here we have used a novel fluorescence lifetime-based assay to identify small-molecule inhibitors of actin-cMyBP-C binding.