Veldhuis Gertjan, Vos Erwin P P, Broos Jaap, Poolman Bert, Scheek Ruud M
Department of Biochemistry and Biophysical Chemistry, Groningen Biomolecular Science and Biotechnology Institute, University of Groningen, 9747 AG Groningen, The Netherlands.
Biophys J. 2004 Apr;86(4):1959-68. doi: 10.1016/S0006-3495(04)74259-9.
Flow dialysis has found widespread use in determining the dissociation constant (KD) of a protein-ligand interaction or the amount of available binding sites (E0). This method has the potency to measure both these parameters in a single experiment and in this article a method to measure simultaneously the KD and E0 is presented, together with an extensive error analysis of the method. The flow-dialysis technique is experimentally simple to perform. However, a number of practical aspects of this method can have a large impact on the outcome of KD and E0. We have investigated all sources of significant systematic and random errors, using the interaction between mannitol and its transporter from Escherichia coli as a model. Monte Carlo simulations were found to be an excellent tool to assess the impact of these errors on the binding parameters and to define the experimental conditions that allow their most accurate estimation.
流动透析已广泛应用于测定蛋白质-配体相互作用的解离常数(KD)或可用结合位点的数量(E0)。该方法有能力在单个实验中测量这两个参数,本文介绍了一种同时测量KD和E0的方法,以及该方法的广泛误差分析。流动透析技术在实验上易于操作。然而,该方法的一些实际方面可能会对KD和E0的结果产生很大影响。我们以甘露醇与其来自大肠杆菌的转运蛋白之间的相互作用为模型,研究了所有显著的系统误差和随机误差来源。发现蒙特卡罗模拟是评估这些误差对结合参数的影响以及确定允许最准确估计这些误差的实验条件的极佳工具。