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-Structure paper
タイトル | Pseudo-repeats in doublecortin make distinct mechanistic contributions to microtubule regulation. |
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ジャーナル・号・ページ | EMBO Rep, Vol. 21, Issue 12, Page e51534, Year 2020 |
掲載日 | 2020年12月3日 |
著者 | Szymon W Manka / Carolyn A Moores / |
PubMed 要旨 | Doublecortin (DCX) is a neuronal microtubule-associated protein (MAP) indispensable for brain development. Its flexibly linked doublecortin (DC) domains-NDC and CDC-mediate microtubule (MT) ...Doublecortin (DCX) is a neuronal microtubule-associated protein (MAP) indispensable for brain development. Its flexibly linked doublecortin (DC) domains-NDC and CDC-mediate microtubule (MT) nucleation and stabilization, but it is unclear how. Using high-resolution time-resolved cryo-EM, we mapped NDC and CDC interactions with tubulin at different MT polymerization stages and studied their functional effects on MT dynamics using TIRF microscopy. Although coupled, each DC repeat within DCX appears to have a distinct role in MT nucleation and stabilization: CDC is a conformationally plastic module that appears to facilitate MT nucleation and stabilize tubulin-tubulin contacts in the nascent MT lattice, while NDC appears to be favored along the mature lattice, providing MT stabilization. Our structures of MT-bound DC domains also explain in unprecedented detail the DCX mutation-related brain defects observed in the clinic. This modular composition of DCX reflects a common design principle among MAPs where pseudo-repeats of tubulin/MT binding elements chaperone or stabilize distinct conformational transitions to regulate distinct stages of MT dynamic instability. |
リンク | EMBO Rep / PubMed:33051979 / PubMed Central |
手法 | EM (単粒子) |
解像度 | 3.8 - 4.2 Å |
構造データ | EMDB-4858, PDB-6rev: |
化合物 | ChemComp-GDP: ChemComp-GTP: ChemComp-MG: ChemComp-PO4: |
由来 |
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キーワード | CYTOSOLIC PROTEIN / Microtubule-associated protein / neuronal migration protein / ubiquitin-like fold / microtubule nucleation and stabilisation / Microtubule-associated protein chimera / microtubule stabilisation |