Motility and microtubule depolymerization mechanisms of the Kinesin-8 motor, KIF19A

作者：Wang Doudou; Nitta Ryo; Morikawa Manatsu; Yajima Hiroaki; Inoue Shigeyuki; Shigematsu Hideki; Kikkawa Masahide; Hirokawa Nobutaka^*

来源：eLife, 2016, 5: e18101.

DOI：10.7554/eLife.18101

The kinesin-8 motor, KIF19A, accumulates at cilia tips and controls cilium length. Defective KIF19A leads to hydrocephalus and female infertility because of abnormally elongated cilia. Uniquely among kinesins, KIF19A possesses the dual functions of motility along ciliary microtubules and depolymerization of microtubules. To elucidate the molecular mechanisms of these functions we solved the crystal structure of its motor domain and determined its cryoelectron microscopy structure complexed with a microtubule. The features of KIF19A that enable its dual function are clustered on its microtubule-binding side. Unexpectedly, a destabilized switch II coordinates with a destabilized L8 to enable KIF19A to adjust to both straight and curved microtubule protofilaments. The basic clusters of L2 and L12 tether the microtubule. The long L2 with a characteristic acidic-hydrophobic-basic sequence effectively stabilizes the curved conformation of microtubule ends. Hence, KIF19A utilizes multiple strategies to accomplish the dual functions of motility and microtubule depolymerization by ATP hydrolysis.

• 出版日期2016-9-30