The adaptor proteins HAP1a and GRIP1 collaborate to activate the kinesin-1 isoform KIF5C

J Cell Sci. 2019 Dec 13;132(24):jcs215822. doi: 10.1242/jcs.215822.

Abstract

Binding of motor proteins to cellular cargoes is regulated by adaptor proteins. HAP1 and GRIP1 are kinesin-1 adaptors that have been implicated individually in the transport of vesicular cargoes in the dendrites of neurons. We find that HAP1a and GRIP1 form a protein complex in the brain, and co-operate to activate the kinesin-1 subunit KIF5C in vitro Based upon this co-operative activation of kinesin-1, we propose a modification to the kinesin activation model that incorporates stabilisation of the central hinge region known to be critical to autoinhibition of kinesin-1.

Keywords: Adaptor proteins; Autoinhibition; Kinesin; Microtubule transport; Molecular motor.

Publication types

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

MeSH terms

  • Animals
  • COS Cells
  • Carrier Proteins / genetics
  • Carrier Proteins / metabolism*
  • Chlorocebus aethiops
  • HeLa Cells
  • Humans
  • Kinesins / genetics
  • Kinesins / metabolism*
  • Microtubules / genetics
  • Microtubules / metabolism
  • Nerve Tissue Proteins / genetics
  • Nerve Tissue Proteins / metabolism*
  • Protein Binding
  • Protein Isoforms / genetics
  • Protein Isoforms / metabolism

Substances

  • Carrier Proteins
  • GRIP1 protein, human
  • HAP1 protein, human
  • Nerve Tissue Proteins
  • Protein Isoforms
  • KIF5C protein, human
  • Kinesins