TY - JOUR
T1 - StableMARK-decorated microtubules in cells have expanded lattices
AU - de Jager, Leanne
AU - Jansen, Klara I
AU - Hoogebeen, Robin
AU - Akhmanova, Anna
AU - Kapitein, Lukas C
AU - Förster, Friedrich
AU - Howes, Stuart C
N1 - Publisher Copyright:
© 2024 de Jager et al.
PY - 2025/1/6
Y1 - 2025/1/6
N2 - Microtubules are crucial in cells and are regulated by various mechanisms like posttranslational modifications, microtubule-associated proteins, and tubulin isoforms. Recently, the conformation of the microtubule lattice has also emerged as a potential regulatory factor, but it has remained unclear to what extent different lattices co-exist within the cell. Using cryo-electron tomography, we find that, while most microtubules have a compacted lattice (∼41 Å monomer spacing), approximately a quarter of the microtubules displayed more expanded lattice spacings. The addition of the microtubule-stabilizing agent Taxol increased the lattice spacing of all microtubules, consistent with results on reconstituted microtubules. Furthermore, correlative cryo-light and electron microscopy revealed that the stable subset of microtubules labeled by StableMARK, a marker for stable microtubules, predominantly displayed a more expanded lattice spacing (∼41.9 Å), further suggesting a close connection between lattice expansion and microtubule stability. The coexistence of different lattices and their correlation with stability implicate lattice spacing as an important factor in establishing specific microtubule subsets.
AB - Microtubules are crucial in cells and are regulated by various mechanisms like posttranslational modifications, microtubule-associated proteins, and tubulin isoforms. Recently, the conformation of the microtubule lattice has also emerged as a potential regulatory factor, but it has remained unclear to what extent different lattices co-exist within the cell. Using cryo-electron tomography, we find that, while most microtubules have a compacted lattice (∼41 Å monomer spacing), approximately a quarter of the microtubules displayed more expanded lattice spacings. The addition of the microtubule-stabilizing agent Taxol increased the lattice spacing of all microtubules, consistent with results on reconstituted microtubules. Furthermore, correlative cryo-light and electron microscopy revealed that the stable subset of microtubules labeled by StableMARK, a marker for stable microtubules, predominantly displayed a more expanded lattice spacing (∼41.9 Å), further suggesting a close connection between lattice expansion and microtubule stability. The coexistence of different lattices and their correlation with stability implicate lattice spacing as an important factor in establishing specific microtubule subsets.
KW - Animals
KW - Cryoelectron Microscopy
KW - Electron Microscope Tomography
KW - Humans
KW - Microtubule-Associated Proteins/metabolism
KW - Microtubules/metabolism
KW - Paclitaxel/pharmacology
KW - Tubulin/metabolism
UR - http://www.scopus.com/inward/record.url?scp=85206281287&partnerID=8YFLogxK
U2 - 10.1083/jcb.202206143
DO - 10.1083/jcb.202206143
M3 - Article
C2 - 39387699
SN - 0021-9525
VL - 224
JO - The Journal of cell biology
JF - The Journal of cell biology
IS - 1
M1 - e202206143
ER -