Abstract
Myosin V is a dimeric molecular motor that moves processively on actin, with the center of mass moving ±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.
Original language | English (US) |
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Pages (from-to) | 2061-2065 |
Number of pages | 5 |
Journal | Science |
Volume | 300 |
Issue number | 5628 |
DOIs | |
State | Published - Jun 27 2003 |
ASJC Scopus subject areas
- General