| Literature DB >> 27717739 |
Anne Houdusse1, H Lee Sweeney2.
Abstract
How myosin interacts with actin to generate force is a subject of considerable controversy. The major debate centers on understanding at what point in force generation the inorganic phosphate is released with respect to the lever arm swing, or powerstroke. Resolving the controversy is essential for understanding how force is produced as well as the mechanisms underlying disease-causing mutations in myosin. Recent structural insights into the powerstroke have come from a high-resolution structure of myosin in a previously unseen state and from an electron cryomicroscopy (cryo-EM) 3D reconstruction of the actin-myosin-MgADP complex. Here, we argue that seemingly contradictory data from time-resolved fluorescence resonance energy transfer (FRET) studies can be reconciled, and we put forward a model for myosin force generation on actin.Entities:
Keywords: allostery; chemo-mechanical transduction; force generation; molecular motors
Mesh:
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Year: 2016 PMID: 27717739 PMCID: PMC5123969 DOI: 10.1016/j.tibs.2016.09.006
Source DB: PubMed Journal: Trends Biochem Sci ISSN: 0968-0004 Impact factor: 13.807