AI Article Synopsis

  • Myosin VI is a unique molecular motor that moves along actin filaments using energy from ATP, and serves both as a vesicle transporter and a cytoskeletal anchor.
  • Recent research has identified that myosin VI can take different types of steps, particularly a special adjacent binding state, where both heads are closely bound to the actin filament, contributing to its unique functionality.
  • New findings show that in the adjacent binding state, the motor's lever arms tilt forward and that either head can move to take the next step, leading to a proposed comprehensive model of how myosin VI operates.

Article 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.

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Source
http://dx.doi.org/10.1002/smll.201200765DOI Listing

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