Brune D, Kim S
Department of Chemical Engineering, University of Wisconsin, Madison 53705.
Proc Natl Acad Sci U S A. 1994 Apr 12;91(8):2930-4. doi: 10.1073/pnas.91.8.2930.
Protein-ligand reaction rates are often limited by the rate of diffusional encounter of the protein and ligand in solution. Reaction rates, however, can be much greater than expected, given the necessity for correct orientation before reaction. A number of forces can affect the orientation of the protein and ligand in solution, and thus increase the reaction rate. We have considered hydrodynamic forces, produced when water molecules between protein and ligand must be pushed out of the way to allow their encounter. We have used the cleft enzymes as a model system, as they could be expected to show strong hydrodynamic effects. One particular type of hydrodynamic interaction stands out: a steering torque which occurs when the enzyme and substrate move toward each other in solution. The magnitude of this steering torque is compared to the mutual torque experienced by interacting "protein-sized" dipoles in solution. A simple model is used to demonstrate that the hydrodynamic steering torque can be 2 orders of magnitude greater than the electrostatic torque.
蛋白质-配体反应速率通常受蛋白质和配体在溶液中扩散相遇速率的限制。然而,鉴于反应前需要正确的取向,反应速率可能比预期的要快得多。许多力会影响蛋白质和配体在溶液中的取向,从而提高反应速率。我们考虑了流体动力,当蛋白质和配体之间的水分子必须被推开以便它们相遇时就会产生这种力。我们以裂隙酶作为模型系统,因为预计它们会表现出强烈的流体动力效应。一种特殊类型的流体动力相互作用尤为突出:当酶和底物在溶液中相互靠近时会出现的转向扭矩。将这种转向扭矩的大小与溶液中相互作用的“蛋白质大小”偶极子所经历的相互扭矩进行了比较。使用一个简单的模型来证明流体动力转向扭矩可能比静电扭矩大两个数量级。