Evidence map›Paper›PMID 40440074›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2025

Microtubule dynamics are defined by conformations and stability of clustered protofilaments.

Maksim Kalutskii, Helmut Grubmüller, Vladimir A Volkov, Maxim Igaev

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Improving Conformational Ensembles of Folded Proteins in Go̅Martini.Journal of chemical theory and computation · 2026
    Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Structural switching of tubulin in the microtubule lattice.Biochemical Society transactions · 2025
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Maksim KalutskiiDepartment of Theoretical and Computational Biophysics, Max Planck Institute for Multidisciplinary Sciences, Göttingen D-37077, Germany.
Helmut GrubmüllerDepartment of Theoretical and Computational Biophysics, Max Planck Institute for Multidisciplinary Sciences, Göttingen D-37077, Germany.ORCID 0000-0002-3270-3144
Vladimir A VolkovCentre for Molecular Cell Biology, School of Biological and Behavioural Sciences, Queen Mary University of London, London E1 4NS, United Kingdom.
Maxim IgaevDepartment of Theoretical and Computational Biophysics, Max Planck Institute for Multidisciplinary Sciences, Göttingen D-37077, Germany.ORCID 0000-0001-8781-1604

Funding

Deutsche Forschungsgemeinschaft (DFG) RTG 2756 Project A1 Project-ID 449750155Max-Planck-Gesellschaft (MPG) Core FundsQueen Mary University of London (QM) SBC8VOL2University of Dundee (Oilthigh Dhùn Dè) Start-Up Funds
6 · The paper itself

Abstract

Microtubules are dynamic cytoskeletal polymers that add and lose tubulin dimers at their ends. Microtubule growth, shortening, and transitions between them are linked to GTP hydrolysis. Recent evidence suggests that flexible tubulin protofilaments at microtubule ends adopt a variety of shapes, complicating structural analysis using conventional techniques. Therefore, the link between GTP hydrolysis, protofilament structure and microtubule polymerization state is poorly understood. Here, we investigate the conformational dynamics of microtubule ends using coarse-grained modeling supported by atomistic simulations and cryoelectron tomography. We show that individual bent protofilaments organize in clusters, transient precursors to the straight microtubule lattice, with GTP-bound ends showing elevated and more persistent cluster formation. Differences in the mechanical properties of GTP- and GDP-protofilaments result in differences in intracluster tension, determining both clustering propensity and protofilament length. We propose that conformational selection at microtubule ends favors long-lived clusters of short GTP-protofilaments that are more prone to forming a straight microtubule lattice and accommodating new tubulin dimers. Conversely, microtubule ends trapped in states with unevenly long and stiff GDP-protofilaments are more prone to shortening. We conclude that protofilament clustering is the key phenomenon that links the hydrolysis state of single tubulins to the polymerization state of the entire microtubule.

Indexed as

MicrotubulesTubulinCryoelectron MicroscopyGuanosine DiphosphateGuanosine TriphosphateHydrolysisMolecular Dynamics SimulationProtein ConformationGuanosine DiphosphateGuanosine TriphosphateTubulincoarse-grained modelingcryoelectron tomographydynamic instabilitymicrotubulemolecular dynamics simulation

Identifiers

PMID40440074
PMCPMC12146719

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.