从增强采样QM/MM模拟中对酶催化物的动态视图
Dhiman Ray1, Sudip Das1, Umberto Raucci1
1Atomistic Simulations, Italian Institute of Technology, Via Enrico Melen 83, Genova GE 16152, Italy.
Journal of chemical information and modeling
|April 12, 2024
概括
这项研究引入了一种新的计算方法,可以直接计算酶反应速率 (kcat). 增强采样QM/MM方法通过考虑动态酶基质相互作用,准确预测酶动力学.
科学领域:
- 生物化学 生物化学
- 计算化学计算化学
- 酶学 是一种酶学.
背景情况:
- 酶动力学 (kcat) 对于理解生物过程至关重要.
- 当前的方法通常依赖于过渡状态理论近似.
- 精确计算酶催化反应速率仍然是一个挑战.
研究的目的:
- 开发一种新的计算方法,用于直接计算酶动力学 (kcat).
- 克服过渡状态理论在酶反应速率计算中的局限性.
- 为了结合酶基质复合体的动态平衡.
主要方法:
- 使用了一种增强的采样量子力学/分子力学 (QM/MM) 方法.
- 直接计算了酶反应的动力学.
- 考虑到反应性和非反应性酶/基质构成之间的动态平衡.
主要成果:
- 计算的kcat值显示了与实验数据的数量顺序一致.
- 在不依赖过渡状态理论假设的情况下成功计算了动力学.
- 在两个代表性的酶反应上证明了该方法的有效性.
结论:
- 增强采样QM/MM方法提供了对酶反应速率 (kcat) 的准确预测.
- 这种方法提供了一种更直接,更全面的方法来研究酶动力学.
- 这些发现对药物设计和理解酶机制有意义.
相关概念视频
Introduction to Enzyme Kinetics
20.0K
Enzyme kinetics studies the rates of biochemical reactions. Scientists monitor the reaction rates for a particular enzymatic reaction at various substrate concentrations. Additional trials with inhibitors or other molecules that affect the reaction rate may also be performed.
The experimenter can then plot the initial reaction rate or velocity (Vo) of a given trial against the substrate concentration ([S]) to obtain a graph of the reaction properties. For many enzymatic reactions involving a...
The experimenter can then plot the initial reaction rate or velocity (Vo) of a given trial against the substrate concentration ([S]) to obtain a graph of the reaction properties. For many enzymatic reactions involving a...
20.0K
Enzyme Kinetics
96.6K
Enzymes speed up reactions by lowering the activation energy of the reactants. The speed at which the enzyme turns reactants into products is called the rate of reaction. Several factors impact the rate of reaction, including the number of available reactants. Enzyme kinetics is the study of how an enzyme changes the rate of a reaction.
Scientists typically study enzyme kinetics with a fixed amount of enzyme in the controlled environment of a test tube. When more reactant, or substrate, is...
Scientists typically study enzyme kinetics with a fixed amount of enzyme in the controlled environment of a test tube. When more reactant, or substrate, is...
96.6K
Introduction to Mechanisms of Enzyme Catalysis
8.1K
For many years, scientists thought that enzyme-substrate binding took place in a simple "lock-and-key" fashion. This model stated that the enzyme and substrate fit together perfectly in one instantaneous step. However, current research supports a more refined view scientists call induced fit. The induced-fit model expands upon the lock-and-key model by describing a more dynamic interaction between enzyme and substrate. As the enzyme and substrate come together, their interaction causes...
8.1K
Catalytically Perfect Enzymes
4.0K
The theory of catalytically perfect enzymes was first proposed by W.J. Albery and J. R. Knowles in 1976. These enzymes catalyze biochemical reactions at high-speed. Their catalytic efficiency values range from 108-109 M-1s-1. These enzymes are also called 'diffusion-controlled' as the only rate-limiting step in the catalysis is that of the substrate diffusion into the active site. Examples include triose phosphate isomerase, fumarase, and superoxide dismutase.
Most enzymes...
Most enzymes...
4.0K
Enzymes
81.5K
Inside living organisms, enzymes act as catalysts for many biochemical reactions involved in cellular metabolism. The role of enzymes is to reduce the activation energies of biochemical reactions by forming complexes with its substrates. The lowering of activation energies favor an increase in the rates of biochemical reactions.
Enzyme deficiencies can often translate into life-threatening diseases. For example, a genetic abnormality resulting in the deficiency of the enzyme G6PD...
Enzyme deficiencies can often translate into life-threatening diseases. For example, a genetic abnormality resulting in the deficiency of the enzyme G6PD...
81.5K
Induced-fit Model
80.8K
Most chemical reactions in cells require enzymes—biological catalysts that speed up the reaction without being consumed or permanently changed. They reduce the activation energy needed to convert the reactants into products. Enzymes are proteins, that usually work by binding to a substrate—a reactant molecule that they act upon.
Enzymes exhibit substrate specificity, meaning that they can only bind to certain substrates. This is mainly determined by the shape and chemical...
Enzymes exhibit substrate specificity, meaning that they can only bind to certain substrates. This is mainly determined by the shape and chemical...
80.8K


