化学
催化作用
动力学(音乐)
极限(数学)
机制(生物学)
同种类的
分子动力学
化学物理
翻译(生物学)
计算化学
蛋白质动力学
构象变化
过渡状态
生化工程
反应机理
化学反应
纳米技术
反应速率
反应动力学
酶催化
反应中间体
均相催化
设计要素和原则
分子构象
反作用坐标
动力学
统计物理学
反应条件
作者
James Gallagher,Emanuele Penocchio,Robert George Bergman,F. Dean Toste
摘要
Conformational changes occur throughout biology and are implicated in numerous phenomena, including enzyme catalysis where their role remains controversial. Conformational dynamics have also been observed in small-molecule catalysis, yet a lack of systematic study means that their influence is poorly understood. Here, we highlight how advances in chemical reaction network mathematics, alongside the translation of the Sabatier principle from heterogeneous to homogeneous catalysis, now enable the behavior of conformationally dynamic catalysts to be understood from first principles. We demonstrate that for common classes of reaction mechanisms, catalyst conformational dynamics can, in principle, cause large rate enhancements relative to each of the catalyst's individual conformations, as well as rate enhancements of orders of magnitude above the Sabatier limit. This quantitative understanding reveals how particular features of a catalyst or reaction mechanism govern catalytic rate, which allows us to propose general design principles that might be exploited by existing or future conformationally dynamic catalysts. The understanding that conformational dynamics can allow a catalyst to overcome otherwise fundamental rate limits should have broad implications across chemistry and biology.
科研通智能强力驱动
Strongly Powered by AbleSci AI