Abstract
Microtubules are dynamic polymers that undergo stochastic transitions between growing and shrinking phases. The structural and chemical properties of these phases remain poorly understood. The transition from growth to shrinkage, termed catastrophe, is not a first-order reaction but rather a multistep process whose frequency increases with the growth time: the microtubule ages as the older microtubule tip becomes more unstable. Aging shows that the growing phase is not a single state but comprises several substates of increasing instability. To investigate whether the shrinking phase is also multistate, we characterized the kinetics of microtubule shrinkage following catastrophe using an in vitro reconstitution assay with purified tubulins. We found that the shrinkage speed is highly variable across microtubules and that the shrinkage speed of individual microtubules slows down over time by as much as several fold. The shrinkage slowdown was observed in both fluorescently labeled and unlabeled microtubules as well as in microtubules polymerized from tubulin purified from different species, suggesting that the shrinkage slowdown is a general property of microtubules. These results indicate that microtubule shrinkage, like catastrophe, is time dependent and that the shrinking microtubule tip passes through a succession of states of increasing stability. We hypothesize that the shrinkage slowdown is due to destabilizing events that took place during growth, which led to multistep catastrophe. This suggests that the aging associated with growth is also manifested during shrinkage, with the older, more unstable growing tip being associated with a faster depolymerizing shrinking tip.
Original language | English |
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Pages (from-to) | 616-623 |
Number of pages | 8 |
Journal | Biophysical Journal |
Volume | 122 |
Issue number | 4 |
Early online date | 19 Jan 2023 |
DOIs | |
State | Published - 21 Feb 2023 |
Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2023 Biophysical Society
Funding
The authors thanks Dr. Maijia Liao, Dr. Olivier Trottier, and Dr. Pei-Zhi Ivy Huang for the fruitful discussions during the development of the project. R.O. was supported by a cross-disciplinary fellowship from Human Frontier Science Program ( LT000919/2015-C ) and a European Molecular Biology Organization long-term fellowship ( ALTF 1424-2014 ). This work was supported by NIH grants R01 GM139337 and R01 NS118884 (to J.H.)
Funders | Funder number |
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National Institutes of Health | R01 GM139337, R01 NS118884 |
European Molecular Biology Organization | ALTF 1424-2014 |
Human Frontier Science Program | LT000919/2015-C |