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Strain stiffening of the Ndc80 complex

Felix Schwietert, Vladimir A. Volkov, View ORCID ProfilePim J. Huis in ‘t Veld, Marileen Dogterom, Andrea Musacchio, View ORCID ProfileJan Kierfeld
doi: https://doi.org/10.1101/2022.03.15.484438
Felix Schwietert
1Physics Department, TU Dortmund University, Dortmund, Germany
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Vladimir A. Volkov
2School of Biological and Behavioural Sciences, Queen Mary University of London, London, UK
3Department of Bionanoscience, Faculty of Applied Sciences, Delft University of Technology, Delft, Netherlands
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Pim J. Huis in ‘t Veld
4Department of Mechanistic Cell Biology, Max Planck Institute of Molecular Physiology, Dortmund, Germany
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  • ORCID record for Pim J. Huis in ‘t Veld
Marileen Dogterom
3Department of Bionanoscience, Faculty of Applied Sciences, Delft University of Technology, Delft, Netherlands
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Andrea Musacchio
4Department of Mechanistic Cell Biology, Max Planck Institute of Molecular Physiology, Dortmund, Germany
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Jan Kierfeld
1Physics Department, TU Dortmund University, Dortmund, Germany
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  • For correspondence: jan.kierfeld@tu-dortmund.de
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ABSTRACT

In the mitotic spindle, microtubules attach to chromosomes via kinetochores. The microtubule-binding Ndc80 complex is an integral part of kinetochores, and is essential for kinetochores to attach to microtubules and to transmit forces from dynamic microtubule ends to the chromosomes. The Ndc80 complex has a rod-like appearance with globular domains at its ends that are separated by a long coiled coil. Its mechanical properties are considered important for the dynamic interaction between kinetochores and microtubules. Here, we present a novel method that allows us to time-trace the effective stiffness of Ndc80 complexes following shortening microtubule ends against applied force in optical trap experiments. Applying this method to wild type Ndc80 and three variants (CH-domains mutated or Hec1-tail unphosphorylated, phosphorylated, or truncated), we reveal that each variant exhibits strain stiffening, i.e., the effective stiffness increases under tension that is built up by a depolymerizing microtubule. The strain stiffening relation is roughly linear and independent of the state of the microtubule. We introduce a polymer model for the Ndc80 complex, which shows that the strain stiffening can be traced back to the specific architecture of the Ndc80 complex with a characteristic flexible kink and the bending elasticity of flaring protofilaments, which exert force to move Ndc80 complexes. Our model accounts for changes in the amount of load-bearing attachments at various force levels and reproduces the roughly linear strain stiffening behavior, highlighting the importance of force-dependent binding affinity.

SIGNIFICANCE By time-tracing the stiffness of microtubule end-tracking Ndc80 complexes in optical trap experiments, we detect strain stiffening, and, thereby, provide new insights into the elastic properties of the Ndc80 complex. The strain stiffening is robust against mutations in the Ndc80 complex. We relate strain stiffening to the structure of the Ndc80 complex by means of a simple polymer model, and to the flexibility of force-generating flaring protofilaments at the tip of the microtubule. Since Ndc80 complexes play a major role for transmitting force from microtubule ends to the kinetochore, their elastic properties are of great interest for a deeper understanding of chromosome dynamics in the mitotic spindle.

Competing Interest Statement

The authors have declared no competing interest.

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC 4.0 International license.
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Posted March 16, 2022.
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Strain stiffening of the Ndc80 complex
Felix Schwietert, Vladimir A. Volkov, Pim J. Huis in ‘t Veld, Marileen Dogterom, Andrea Musacchio, Jan Kierfeld
bioRxiv 2022.03.15.484438; doi: https://doi.org/10.1101/2022.03.15.484438
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Strain stiffening of the Ndc80 complex
Felix Schwietert, Vladimir A. Volkov, Pim J. Huis in ‘t Veld, Marileen Dogterom, Andrea Musacchio, Jan Kierfeld
bioRxiv 2022.03.15.484438; doi: https://doi.org/10.1101/2022.03.15.484438

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