Myosin V and Kinesin act as tethers to enhance each others' processivity
-
Edited by Edward D. Korn, National Institutes of Health, Bethesda, MD, and approved January 22, 2008 (received for review December 6, 2007)
Abstract
Organelle transport to the periphery of the cell involves coordinated transport between the processive motors kinesin and myosin V. Long-range transport takes place on microtubule tracks, whereas final delivery involves shorter actin-based movements. The concept that motors only function on their appropriate track required further investigation with the recent observation that myosin V undergoes a diffusional search on microtubules. Here we show, using single-molecule techniques, that a functional consequence of myosin V's diffusion on microtubules is a significant enhancement of the processive run length of kinesin when both motors are present on the same cargo. The degree of run length enhancement correlated with the net positive charge in loop 2 of myosin V. On actin, myosin V also undergoes longer processive runs when kinesin is present on the same cargo. The process that causes run length enhancement on both cytoskeletal tracks is electrostatic. We propose that one motor acts as a tether for the other and prevents its diffusion away from the track, thus allowing more steps to be taken before dissociation. The resulting run length enhancement likely contributes to the successful delivery of cargo in the cell.
Footnotes
- *To whom correspondence may be addressed. E-mail: warshaw{at}physiology.med.uvm.edu or kathleen.trybus{at}uvm.edu
-
Author contributions: M.Y.A. and H.L. contributed equally to this work; M.Y.A., H.L., D.M.W., and K.M.T. designed research; M.Y.A. and H.L. performed research; C.S.B. and K.M.T. contributed new reagents/analytic tools; M.Y.A. and H.L. analyzed data; and M.Y.A., H.L., D.M.W., and K.M.T. wrote the paper.
-
The authors declare no conflict of interest.
-
This article is a PNAS Direct Submission.
-
This article contains supporting information online at www.pnas.org/cgi/content/full/0711531105/DC1.
- © 2008 by The National Academy of Sciences of the USA





