| Literature DB >> 12791999 |
Ahmet Yildiz1, Joseph N Forkey, Sean A McKinney, Taekjip Ha, Yale E Goldman, Paul R Selvin.
Abstract
Myosin V is a dimeric molecular motor that moves processively on actin, with the center of mass moving approximately 37 nanometers for each adenosine triphosphate hydrolyzed. We have labeled myosin V with a single fluorophore at different positions in the light-chain domain and measured the step size with a standard deviation of <1.5 nanometers, with 0.5-second temporal resolution, and observation times of minutes. The step size alternates between 37 + 2x nm and 37 - 2x, where x is the distance along the direction of motion between the dye and the midpoint between the two heads. These results strongly support a hand-over-hand model of motility, not an inchworm model.Entities:
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Year: 2003 PMID: 12791999 DOI: 10.1126/science.1084398
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728