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VASH1-SVBP and VASH2-SVBP Generate Different Detyrosination Profiles on Microtubules

Abstract

The detyrosination/tyrosination cycle of α-tubulin is critical for proper cell functioning. VASH1-SVBP and VASH2-SVBP are ubiquitous enzymes involved in microtubule detyrosination, whose mode of action is little known. Here, we show in reconstituted systems and cells that VASH1-SVBP and VASH2-SVBP drive the global and local detyrosination of microtubules, respectively. We solved the cryo-electron microscopy structure of VASH2-SVBP bound to microtubules, revealing a different microtubule-binding configuration of its central catalytic region compared to VASH1-SVBP. We show that the divergent mode of detyrosination between the two enzymes is correlated with the microtubule-binding properties of their disordered N- and C-terminal regions. Specifically, the N-terminal region is responsible for a significantly longer residence time of VASH2-SVBP on microtubules compared to VASH1-SVBP. We suggest that this VASH region is critical for microtubule detachment and diffusion of VASH-SVBP enzymes on lattices. Our results suggest a mechanism by which VASH1-SVBP and VASH2-SVBP could generate distinct microtubule subpopulations and confined areas of detyrosinated lattices to drive various microtubule-based cellular functions.

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References
1.
Stoppin-Mellet V, Bagdadi N, Saoudi Y, Arnal I . Studying Tau-Microtubule Interaction Using Single-Molecule TIRF Microscopy. Methods Mol Biol. 2019; 2101:77-91. DOI: 10.1007/978-1-0716-0219-5_6. View

2.
Li F, Hu Y, Qi S, Luo X, Yu H . Structural basis of tubulin detyrosination by vasohibins. Nat Struct Mol Biol. 2019; 26(7):583-591. PMC: 6609488. DOI: 10.1038/s41594-019-0242-x. View

3.
Chen V, Arendall 3rd W, Headd J, Keedy D, Immormino R, Kapral G . MolProbity: all-atom structure validation for macromolecular crystallography. Acta Crystallogr D Biol Crystallogr. 2010; 66(Pt 1):12-21. PMC: 2803126. DOI: 10.1107/S0907444909042073. View

4.
Peris L, Parato J, Qu X, Soleilhac J, Lante F, Kumar A . Tubulin tyrosination regulates synaptic function and is disrupted in Alzheimer's disease. Brain. 2022; 145(7):2486-2506. PMC: 9337816. DOI: 10.1093/brain/awab436. View

5.
Landskron L, Bak J, Adamopoulos A, Kaplani K, Moraiti M, van den Hengel L . Posttranslational modification of microtubules by the MATCAP detyrosinase. Science. 2022; 376(6595):eabn6020. DOI: 10.1126/science.abn6020. View