| Literature DB >> 22777889 |
Keigo Ikezaki1, Tomotaka Komori, Mitsuhiro Sugawa, Yoshiyuki Arai, So Nishikawa, Atsuko H Iwane, Toshio Yanagida.
Abstract
Myosin VI is an adenosine triphosphate (ATP)-driven dimeric molecular motor that has dual function as a vesicle transporter and a cytoskeletal anchor. Recently, it was reported that myosin VI generates three types of steps by taking either a distant binding or adjacent binding state (noncanonical hand-over-hand step pathway). The adjacent binding state, in which both heads bind to an actin filament near one another, is unique to myosin VI and therefore may help explain its distinct features. However, detailed information of the adjacent binding state remains unclear. Here simultaneous observations of the head and tail domain during stepping are presented. These observations show that the lever arms tilt forward in the adjacent binding state. Furthermore, it is revealed that either head could take the subsequent step with equal probability from this state. Together with previous results, a comprehensive stepping scheme is proposed; it includes the tail domain motion to explain how myosin VI achieves its dual function.Entities:
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Year: 2012 PMID: 22777889 DOI: 10.1002/smll.201200765
Source DB: PubMed Journal: Small ISSN: 1613-6810 Impact factor: 13.281