Gulliver, CNRS, ESPCI, Université PSL, Paris, France.
Biophys J. 2024 Jun 18;123(12):1563-1578. doi: 10.1016/j.bpj.2024.04.030. Epub 2024 May 3.
The role played by conformational changes in enzyme catalysis is controversial. In addition to examining specific enzymes, studying formal models can help identify the conditions under which conformational changes promote catalysis. Here, we present a model demonstrating how conformational changes can break a generic trade-off due to the conflicting requirements of successive steps in catalytic cycles, namely high specificity for the transition state to accelerate the chemical transformation and low affinity for the products to favor their release. The mechanism by which the trade-off is broken is a transition between conformations with different affinities for the substrate. The role of the effector that induces the transition is played by a substrate "handle," a part of the substrate that is not chemically transformed but whose interaction with the enzyme is nevertheless essential to rapidly complete the catalytic cycle. A key element of the model is the formalization of the constraints causing the trade-off that the presence of multiple states breaks, which we attribute to the strong chemical similarity between successive reaction states-substrates, transition states, and products. For the sake of clarity, we present our model for irreversible one-step unimolecular reactions. In this context, we demonstrate how the different forms that chemical similarities between reaction states can take impose limits on the overall catalytic turnover. We first analyze catalysts without internal degrees of freedom and then show how two-state catalysts can overcome their limitations. Our results recapitulate previous proposals concerning the role of conformational changes and substrate handles in a formalism that makes explicit the constraints that elicit these features. In addition, our approach establishes links with studies in the field of heterogeneous catalysis, where the same trade-offs are observed and where overcoming them is a well-recognized challenge.
构象变化在酶催化中的作用颇具争议。除了研究特定的酶,研究形式模型还可以帮助确定构象变化促进催化的条件。在这里,我们提出了一个模型,展示了构象变化如何打破由于催化循环中连续步骤的冲突要求而导致的通用权衡,即高特异性过渡态以加速化学转化和低亲和力产物以有利于其释放。打破权衡的机制是具有不同底物亲和力的构象之间的转变。诱导这种转变的效应物的作用由底物“手柄”来发挥,底物“手柄”是底物的一部分,它没有发生化学转化,但与酶的相互作用对于快速完成催化循环仍然是必不可少的。该模型的一个关键要素是形式化导致权衡的约束,而这种约束是由连续反应状态(底物、过渡态和产物)之间强烈的化学相似性引起的。为了清晰起见,我们提出了我们的不可逆一步单分子反应模型。在这个上下文中,我们展示了反应状态之间化学相似性可以采取的不同形式如何对整体催化周转率施加限制。我们首先分析没有内部自由度的催化剂,然后展示了两态催化剂如何克服其局限性。我们的结果概括了以前关于构象变化和底物手柄在使这些特征显式化的形式主义中的作用的建议。此外,我们的方法与多相催化领域的研究建立了联系,在该领域也观察到了相同的权衡,并且克服这些权衡是一个公认的挑战。