Motor number controls cargo switching at actin-microtubule intersections in vitro

Curr Biol. 2010 Apr 27;20(8):687-96. doi: 10.1016/j.cub.2010.03.024. Epub 2010 Apr 15.

Abstract

Background: Cellular activities such as endocytosis and secretion require that cargos actively switch between the microtubule (MT) and actin filament (AF) networks. Cellular studies suggest that switching may involve a tug of war or coordinate regulation of MT- and AF-based motor function.

Results: To test the hypothesis that motor number can be used to direct the outcome of a tug-of-war process, we reconstituted cargo switching at MT-AF intersections in a minimal system with purified myosin V and dynein-dynactin motors bound to beads. Beads containing both motors often paused at the intersections and rotated about an axis perpendicular to both filaments, suggesting that competing motors apply a torque on their cargo. Force measurements showed that motor forces scale with the number of engaged myosin V and dynein-dynactin motors. Whether beads remained on a MT or AF or switched to the alternate track was determined by which set of motors collectively produced greater force. Passing and switching probabilities were similar whether the bead approached an intersection on either a MT or an AF. Beads with a force ratio near unity had approximately equal probabilities of exiting on the MT, exiting on the AF, or remaining stalled at the intersection. A simple statistical model quantitatively describes the relationship between switching probability and motor number.

Conclusions: Cargo switching can be tuned via combinations of 1-4 myosin V and 1-4 dynein-dynactin engaged motors through a simple force-mediated mechanism.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Actin Cytoskeleton / metabolism*
  • Actin Cytoskeleton / ultrastructure
  • Animals
  • Biological Transport / physiology*
  • Cattle
  • Chickens
  • Dynactin Complex
  • Dyneins / metabolism
  • Microtubule-Associated Proteins / metabolism
  • Microtubules / metabolism*
  • Microtubules / ultrastructure
  • Models, Biological
  • Molecular Motor Proteins / metabolism*
  • Myosin Type V / metabolism
  • Rabbits
  • Rotation
  • Stress, Mechanical

Substances

  • Dynactin Complex
  • Microtubule-Associated Proteins
  • Molecular Motor Proteins
  • Myosin Type V
  • Dyneins