<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Cassidy AC</submitter><funding>NEI NIH HHS</funding><funding>NIDDK NIH HHS</funding><funding>NCI NIH HHS</funding><funding>NIGMS NIH HHS</funding><pubmed_abstract>Microtubule dynamics change during cell division to enable rapid microtubule network remodeling. The switching from microtubule growth to shrinkage is attributed to the loss of a stabilizing GTP-cap structure at the growing microtubule end. The size of the GTP-cap is a result of a balance between GTP-tubulin addition to the microtubule end and subsequent GTP-hydrolysis in the microtubule lattice. Whether the cell-cycle-dependent changes in microtubule dynamics are supported by concurrent modulation of the stabilizing GTP-cap size is not known. Here, we use high spatiotemporal resolution live-cell imaging of EB1, an established marker for the GTP-cap, to directly determine the relationship between GTP-cap size and microtubule growth rate throughout the cell cycle. Our data reveal that GTP-c</pubmed_abstract><journal>bioRxiv : the preprint server for biology</journal><pagination>2026.01.13.699367</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12871301</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>The microtubule GTP-tubulin cap size is modulated during cell division.</pubmed_title><pmcid>PMC12871301</pmcid><funding_grant_id>P30 CA068485</funding_grant_id><funding_grant_id>R35 GM125028</funding_grant_id><funding_grant_id>P30 DK058404</funding_grant_id><funding_grant_id>P30 EY008126</funding_grant_id><funding_grant_id>R35 GM119552</funding_grant_id><pubmed_authors>Zanic M</pubmed_authors><pubmed_authors>Burnette DT</pubmed_authors><pubmed_authors>Cassidy AC</pubmed_authors></additional><is_claimable>false</is_claimable><name>The microtubule GTP-tubulin cap size is modulated during cell division.</name><description>Microtubule dynamics change during cell division to enable rapid microtubule network remodeling. The switching from microtubule growth to shrinkage is attributed to the loss of a stabilizing GTP-cap structure at the growing microtubule end. The size of the GTP-cap is a result of a balance between GTP-tubulin addition to the microtubule end and subsequent GTP-hydrolysis in the microtubule lattice. Whether the cell-cycle-dependent changes in microtubule dynamics are supported by concurrent modulation of the stabilizing GTP-cap size is not known. Here, we use high spatiotemporal resolution live-cell imaging of EB1, an established marker for the GTP-cap, to directly determine the relationship between GTP-cap size and microtubule growth rate throughout the cell cycle. Our data reveal that GTP-c</description><dates><release>2026-01-01T00:00:00Z</release><publication>2026 Jan</publication><modification>2026-07-06T03:17:58.423Z</modification><creation>2026-07-06T03:11:41.171Z</creation></dates><accession>S-EPMC12871301</accession><cross_references><pubmed>41648122</pubmed><doi>10.64898/2026.01.13.699367</doi></cross_references></HashMap>