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        <identifier>oai:figshare.com:article/34023669</identifier>
        <datestamp>2026-09-29T12:11:09Z</datestamp>
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          <dc:title>Taxol acts differently on different tubulin isotypes</dc:title>
          <dc:creator>Yean Ming Chew (24951808)</dc:creator>
          <dc:creator>Robert A. Cross (7579400)</dc:creator>
          <dc:subject>Paclitaxel</dc:subject>
          <dc:subject>Tubulins</dc:subject>
          <dc:subject>Microtubules</dc:subject>
          <dc:subject>Kinesin</dc:subject>
          <dc:subject>Biophysics</dc:subject>
          <dc:subject>Migrated from ePrints</dc:subject>
          <dc:description>Taxol is a small molecule effector that allosterically locks tubulin into the microtubule lattice. We show here that taxol has different effects on different single-isotype microtubule lattices. Using in vitro reconstitution, we demonstrate that single-isotype α1β4 GDP-tubulin lattices are stabilised and expanded by 10 μM taxol, as reported by accelerated microtubule gliding in kinesin motility assays, whereas single-isotype α1β3 GDP-tubulin lattices are stabilised but not expanded. This isotype-specific action of taxol drives gliding of segmented-isotype GDP-taxol microtubules along convoluted, sinusoidal paths, because their expanded α1β4 segments try to glide faster than their compacted α1β3 segments. In GMPCPP, single-isotype α1β3 and α1β4 lattices both show accelerated gliding, indicating that both can in principle be driven to expand. We therefore propose that taxol-induced lattice expansion requires a higher taxol occupancy than taxol-induced stabilisation, and that higher taxol occupancies are accessible to α1β4 but not α1β3 single-isotype lattices.</dc:description>
          <dc:date>2023-09-16T00:00:00Z</dc:date>
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          <dc:identifier>10.1038/s42003-023-05306-y|</dc:identifier>
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