English
 
Help Privacy Policy Disclaimer
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT

Released

Journal Article

Kinesin-14 motors drive a right-handed helical motion of antiparallel microtubules around each other.

MPS-Authors
/persons/resource/persons219458

Mitra,  Aniruddha
Max Planck Institute for Molecular Cell Biology and Genetics, Max Planck Society;

/persons/resource/persons246982

Renger,  Roman
Max Planck Institute for Molecular Cell Biology and Genetics, Max Planck Society;

/persons/resource/persons219596

Ruhnow,  Felix
Max Planck Institute for Molecular Cell Biology and Genetics, Max Planck Society;

/persons/resource/persons219112

Diez,  Stefan
Max Planck Institute for Molecular Cell Biology and Genetics, Max Planck Society;

External Resource
No external resources are shared
Fulltext (restricted access)
There are currently no full texts shared for your IP range.
Fulltext (public)
There are no public fulltexts stored in PuRe
Supplementary Material (public)
There is no public supplementary material available
Citation

Mitra, A., Meißner, L., Gandhimathi, R., Renger, R., Ruhnow, F., & Diez, S. (2020). Kinesin-14 motors drive a right-handed helical motion of antiparallel microtubules around each other. Nature communications, 11(1): 2565. doi:10.1038/s41467-020-16328-z.


Cite as: https://hdl.handle.net/21.11116/0000-0008-A2D6-F
Abstract
Within the mitotic spindle, kinesin motors cross-link and slide overlapping microtubules. Some of these motors exhibit off-axis power strokes, but their impact on motility and force generation in microtubule overlaps has not been investigated. Here, we develop and utilize a three-dimensional in vitro motility assay to explore kinesin-14, Ncd, driven sliding of cross-linked microtubules. We observe that free microtubules, sliding on suspended microtubules, not only rotate around their own axis but also move around the suspended microtubules with right-handed helical trajectories. Importantly, the associated torque is large enough to cause microtubule twisting and coiling. Further, our technique allows us to measure the in situ spatial extension of the motors between cross-linked microtubules to be about 20 nm. We argue that the capability of microtubule-crosslinking kinesins to cause helical motion of overlapping microtubules around each other allows for flexible filament organization, roadblock circumvention and torque generation in the mitotic spindle.