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CYK4 relaxes the bias in the off-axis motion by MKLP1 kinesin-6.

Yohei MaruyamaMitsuhiro SugawaShin YamaguchiTim DaviesToshihisa OsakiTakuya KobayashiMasahiko YamagishiShoji TakeuchiMasanori MishimaJunichiro Yajima
Published in: Communications biology (2021)
Centralspindlin, a complex of the MKLP1 kinesin-6 and CYK4 GAP subunits, plays key roles in metazoan cytokinesis. CYK4-binding to the long neck region of MKLP1 restricts the configuration of the two MKLP1 motor domains in the centralspindlin. However, it is unclear how the CYK4-binding modulates the interaction of MKLP1 with a microtubule. Here, we performed three-dimensional nanometry of a microbead coated with multiple MKLP1 molecules on a freely suspended microtubule. We found that beads driven by dimeric MKLP1 exhibited persistently left-handed helical trajectories around the microtubule axis, indicating torque generation. By contrast, centralspindlin, like monomeric MKLP1, showed similarly left-handed but less persistent helical movement with occasional rightward movements. Analysis of the fluctuating helical movement indicated that the MKLP1 stochastically makes off-axis motions biased towards the protofilament on the left. CYK4-binding to the neck domains in MKLP1 enables more flexible off-axis motion of centralspindlin, which would help to avoid obstacles along crowded spindle microtubules.
Keyphrases
  • computed tomography
  • binding protein
  • mass spectrometry
  • high speed
  • contrast enhanced
  • dna binding
  • solid state