核酸对多种蛋白质类的绝对和相对约束自由能量计算
Apoorva Purohit1, Xiaolin Cheng1
1Division of Medicinal Chemistry and Pharmacognosy, College of Pharmacy, and Translational Data Analytics Institute, The Ohio State University, Columbus, Ohio 43210, United States.
Journal of chemical theory and computation
|December 19, 2024
概括
化学自由能量模拟准确地预测了许多酶的核酸-蛋白质结合. 然而,充电联体,构造变化和双价离子仍然存在挑战,需要进一步精细化模拟.
科学领域:
- 生物化学 生物化学
- 计算化学计算化学
- 结构生物学 结构生物学
背景情况:
- 像ATP和GTP这样的多酸盐核酸对蛋白质功能至关重要.
- 由于连接体的灵活性和电荷,计算它们的结合自由能量具有挑战性.
- 现有的计算方法面临这些复杂相互作用的局限性.
研究的目的:
- 评估核酸与蛋白质结合的化学自由能量模拟的准确性.
- 在建模这些相互作用时评估固定电荷力场.
- 识别局限性并指导未来的计算策略.
主要方法:
- 对与九种不同的蛋白质结合的四个核酸进行了炼化自由能量模拟.
- 固定电荷的力场被用来建模相互作用.
- 实验性的结合自由能量被用于验证.
主要成果:
- 模拟准确地复制了蛋白质的实验结合自由能量,没有显著的结构变化 (87.5%在±2 kcal/mol绝对值内,88.9%在±3 kcal/mol相对值内).
- 当包括双价离子时,观察到不准确性,表明非极化力场的局限性.
- 对于高电荷的柔性联结体,需要进行广泛的构造性采样.
结论:
- 炼金术模拟可靠地预测核酸与蛋白质的结合,当构造变化最小时.
- 当前的力场在这些系统中与双价离子相互作用作斗争.
- 经过验证的模拟策略可以帮助预测核酸模拟对蛋白质标的结合.
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