How Myosin Generates Force on Actin Filaments
2016; Elsevier BV; Volume: 41; Issue: 12 Linguagem: Inglês
10.1016/j.tibs.2016.09.006
ISSN1362-4326
AutoresAnne Houdusse, H. Lee Sweeney,
Tópico(s)Cellular Mechanics and Interactions
ResumoHow 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.
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