人类脂肪酸合成酶与Denifanstat复合体中的核心修饰区域的原子模型
S M Naimul Hasan1, Jennifer W Lou1, Alexander F A Keszei2
1Department of Medical Biophysics, University of Toronto, Toronto, Ontario, Canada.
Nature communications
|June 12, 2023
概括
研究人员为结构研究设计了人类脂肪酸合成酶 (hFASN). 这项工作揭示了脱水酶二聚体.
科学领域:
- 生物化学 生物化学
- 结构生物学 结构生物学
- 药物发现 药物发现 药物发现
背景情况:
- 脂肪酸合成酶 (FASN) 对脂质代谢和信号传递至关重要.
- FASN是癌症,糖尿病和肝脏疾病的关键药物标.
研究的目的:
- 开发一个工程人类FASN (hFASN) 用于结构分析.
- 为了确定hFASN核心修饰区域的冷-EM结构.
- 为了研究hFASN的结构动力学和抑制剂结合.
主要方法:
- 工程全长人类FASN (hFASN) 的表达和净化.
- 电子冷显微镜 (cryo-EM) 用于结构的确定.
- 分析蛋白质结构变化和抑制剂复合结构的分析.
主要成果:
- 确定了hFASN核心修饰区域的2.7 Å冷-EM结构.
- 在脱水酶二聚体中发现了一个独特的,封闭的催化腔.
- 描述了hFASN区域的两个主要的全球构造变异性.
- 解决了hFASN与抗癌药物Denifanstat (TVB-2640) 结合的结构.
结论:
- 设计的hFASN是结构研究的宝贵工具.
- 对hFASN的结构洞察力可以指导新型抑制剂的开发.
- 该平台为针对hFASN的向疗法提供基于结构的药物设计.
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