微管蛋白
GTP'
微管
GTP酶
鸟苷二磷酸
鸟嘌呤核苷酸交换因子
细胞生物学
核苷酸
生物
微管相关蛋白
化学
鸟苷三磷酸
生物化学
酶
基因
作者
Wesley J. Yon,Taekjip Ha,Yixian Zheng,Ross T.A. Pedersen
标识
DOI:10.1016/j.jbc.2025.110401
摘要
α- and β-tubulin form GTPase heterodimers and assemble into microtubules. Like other GTPases, the tubulin heterodimer's nucleotide-bound state regulates its activity. In the dimer, α-tubulin is constitutively bound to GTP, while β-tubulin can bind to either GDP (GDP-tubulin) or GTP (GTP-tubulin). Following assembly into microtubules, GTP-tubulin hydrolyzes GTP to GDP, triggering microtubule disassembly. This generates free GDP-tubulin, which must exchange GDP for GTP to undergo assembly again. Tubulin dimers undergo rapid nucleotide exchange in vitro, leading to a commonly accepted belief that a tubulin guanine nucleotide exchange factor (GEF) may be unnecessary for microtubule assembly in cells. Here, we use quantitative binding assays to show that BuGZ, a spindle assembly factor, binds tightly to GDP-tubulin, less tightly to GTP-tubulin, and weakly to microtubules. We further show that BuGZ promotes the incorporation of GTP into tubulin using a nucleotide exchange assay. The discovery of a tubulin GEF suggests a mechanism that may aid rapid microtubule assembly dynamics in cells.
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