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论蛋白质的电荷调节

On the charge regulation of proteins.

作者信息

Lund Mikael, Jönsson Bo

机构信息

Theoretical Chemistry, Chemical Center, Post Office Box 124, S-221 00 Lund, Sweden.

出版信息

Biochemistry. 2005 Apr 19;44(15):5722-7. doi: 10.1021/bi047630o.

Abstract

It is known that the overall charge of a protein can change as the molecule approaches a charged object like another protein or a cell membrane. We have formalized this mechanism using a statistical mechanical framework and show how this rather overlooked interaction increases the attraction between protein molecules. From the theory, we can identify a unique property, the protein charge capacitance, that contains all information needed to describe the charge regulation mechanism. The capacitance can be obtained from experiment or theory and is a function of pH, salt concentration, and the number of titrating residues. For a range of different protein molecules, we calculate the capacitance and demonstrate how it can be used to quantify the charge regulation interaction. With minimal effort, the derived formulas can be used to improve existing models by including a charge regulation term. Good agreement is found between theory, simulations, and experimental data.

摘要

众所周知,当蛋白质分子靠近带电荷的物体(如另一种蛋白质或细胞膜)时,其整体电荷会发生变化。我们已使用统计力学框架将这一机制形式化,并展示了这种相当被忽视的相互作用是如何增强蛋白质分子间吸引力的。从该理论中,我们可以确定一个独特的属性,即蛋白质电荷电容,它包含描述电荷调节机制所需的所有信息。电容可通过实验或理论获得,并且是pH值、盐浓度和可滴定残基数量的函数。对于一系列不同的蛋白质分子,我们计算了电容,并展示了如何用它来量化电荷调节相互作用。只需付出最小的努力,通过纳入电荷调节项,导出的公式就可用于改进现有模型。理论、模拟和实验数据之间取得了良好的一致性。

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