基酸 (ATP) 在全质上调节一个基-CoA氧化酶
David H Perez1, Arup Mondal1, Weijie Xu1
1Department of Chemistry, University of Florida, Gainesville, FL, 32611, USA.
Nature communications
|August 8, 2025
概括
亚丁三酸盐 (ATP) 通过增强其与FAD辅因子的结合来全质调节-CoA氧化酶 (ACOX). 这一发现揭示了一个新的调节机制,将ATP水平与脂肪酸和二次代谢联系起来.
科学领域:
- 生物化学 生物化学
- 酶学 是一种酶学.
- 代谢调节 代谢调节 代谢调节
背景情况:
- 乙-CoA氧化酶 (ACOX) 酶在多氧体脂肪酸代谢和各种生物的二次代谢中至关重要.
- 这些酶在二聚体界面内的独特位点与典型的基质结合位点不同,结合腺三酸盐 (ATP).
研究的目的:
- 阐明ATP调节ACOX酶活性的机制.
- 研究ATP结合的特异性及其对辅因子亲和力的影响.
主要方法:
- 采用X射线晶体学研究了二极化酶结构.
- 用分子动力学模拟来理解ATP结合及其影响.
- 进行了位点导向的突变发生,以探测ATP结合位点的作用.
主要成果:
- ATP 通过增加酶对其黄氨酸二核酸 (FAD) 辅因子的亲和力来特别刺激 ACOX 活性.
- 通过前所未有的阿尔法螺旋捆的转移来促进ATP结合,从而允许访问埋藏的二分体接口位置.
- 一个全osteric 网络连接ATP和FAD结合点,调解刺激效应.
结论:
- 基酸 (ATP) 通过全质控制ACOX酶与FAD的结合,从而调节酶活性.
- 这种调节机制表明细胞ATP水平与初级和二级代谢途径之间的潜在联系.
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