4.8 Article

Structural Model for Tubulin Recognition and Deformation by Kinesin-13 Microtubule Depolymerases

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CELL REPORTS
卷 3, 期 3, 页码 759-768

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CELL PRESS
DOI: 10.1016/j.celrep.2013.01.030

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资金

  1. National Center for Research Resources, National Institutes of Health (NIH) [C06 RR017528-01-CEM]
  2. NIH [S10 RR17291, R01-GM083338]

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To elucidate the structural basis of the mechanism of microtubule depolymerization by kinesin-13s, we analyzed complexes of tubulin and the Drosophila melanogaster kinesin-13 KLP10A by electron microscopy (EM) and fluorescence polarization microscopy. We report a nanometer-resolution (1.1 nm) cryo-EM three-dimensional structure of the KLP10A head domain (KLP10AHD) bound to curved tubulin. We found that binding of KLP10AHD induces a distinct tubulin configuration with displacement (shear) between tubulin subunits in addition to curvature. In this configuration, the kinesin-binding site differs from that in straight tubulin, providing an explanation for the distinct interaction modes of kinesin-13s with the microtubule lattice or its ends. The KLP10AHD-tubulin interface comprises three areas of interaction, suggesting a crossbow-type tubulin-bending mechanism. These areas include the kinesin-13 family conserved KVD residues, and as predicted from the crossbow model, mutating these residues changes the orientation and mobility of KLP10AHDs interacting with the microtubule.

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