Biophysical JournalBiophysicsPeer-reviewed journal article
On the Curvature and Relaxation of Microtubule Plus-endTips
Tomasz SkóraiD, Jiangbo WuiD, Daniel BeckettiD, Weizhi XueiD, Gregory A. VothiD, Tamara C. BidoneiD
Abstract
Microtubules are essential cytoskeletal components with a broad range of functions in which the structure and dynamics of their plus-end tips play critical roles. Existing mechanistic models explain the tips curving dynamics in different ways: the allosteric model suggests that GTP hydrolysis induces conformational changes in tubulin subunits that destabilize the lattice, leading to protofilament curving and depolymerization, while the lattice model posits that GTP hydrolysis directly destabilizes the microtubule lattice. However, the effect of GTP hydrolysis on the curving dynamics of microtubule tips remains incompletely understood. In this study, we employed a multiscale modeling approach, combining all-atom molecular dynamics simulations with Brownian dynamics simulations, to investigate the relaxation of microtubule plus-end tips into curved configurations. Our results show that both GDP- and GTP-bound tips exhibit an outward bending of protofilaments into curved, rams horn-like structures, characterized by a linear relationship between curvature and distance from the plus-end tip. These observations align with experimental cryo-ET images of microtubule plus-end tips in different nucleotide states. Collectively, our findings suggest that the outward bending of protofilaments at the plus-end tip is an intrinsic feature of microtubules, independent of the nucleotide state. SIGNIFICANCEUnderstanding how microtubules change shape is crucial for elucidating key cellular processes such as cell division and shape maintenance, which are fundamental to both physiological function and disease progression. This study supports the concept that the microtubule plus-end tip relaxation does not align with models that couple shape changes to GTP hydrolysis, at least for the topmost tubulin heterodimers. By interfacing bottom-up multiscale modeling -- using the longest reported atomistic molecular dynamics simulations of microtubule tips-- with existing cryo-ET data, it is shown that protofilament bending operates independently of nucleotide hydrolysis and likely depolymerization. These findings highlight the need for a new conceptual framework that separates GTP hydrolysis from microtubule tip flaring.
- assay: structural biology
- research focus: protein folding & dynamics
- approach: deep learning
- approach: statistical model
- approach: simulation
- Citations
- 1
- FWCI
- 0.50
- Field percentile
- top 41%
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Bending-torsional elasticity and energetics of the plus-end microtubule tip
M. Igaev, H. Grubmueller·bioRxiv·Aug 12, 2021
- Microtubule dynamics are defined by conformations and stability of clustered protofilaments
Maksim A. Kalutskii, Helmut Grubmüller, … Maxim Igaev·Proceedings of the National Academy of SciencesPeer-reviewed·May 29, 2025
- Atomistic basis of microtubule dynamic instability assessed via multiscale modeling
M. Hemmat, D. J. Odde·bioRxiv·Jan 7, 2020
- Evidence for conformational change-induced hydrolysis of β-tubulin-GTP
M. Paydar, B. H. Kwok·bioRxiv·Sep 8, 2020
- Lattice Instability Drives Formation of Protofilament Clusters at the Microtubule Plus End Tips
Weizhi Xue, Jiangbo Wu, … Gregory A. Voth·Biophysical JournalPeer-reviewed·Feb 14, 2026
- Structural transitions in the GTP cap visualized by cryo-EM of catalytically inactive microtubules
B. J. LaFrance, J. Roostalu, … E. Nogales·bioRxiv·Aug 13, 2021