竞争结合分析的数学理论:一个精确而实用的模型。

Receptors & signal transduction Pub Date : 1997-01-01
Q H Chen, D B Bylund
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引用次数: 0

摘要

在竞争性结合试验的通常公式中,各种未标记配体的游离浓度由其总浓度的已知值近似,因为游离浓度不易确定。虽然以前已经推导出方程,给出了以未标记配体的自由浓度作为变量的精确解,但这些方程在实践中没有用处。我们设计了一个竞争结合的数学模型,该模型对一个标记配体、任意数量的未标记配体和任意数量的结合位点的一般情况都是精确和实用的。在该模型中,未标记配体的总浓度是显式变量,而不是它们的自由浓度。未标记配体的游离浓度可由模型估计。该模型是基于质量作用定律和稀释原理,以及一个新的概念,称为等效竞争约束原理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mathematical theory of competitive binding assays: an exact and practical model.

In the usual formulation of the equations for competitive binding assays, the free concentrations of the various unlabeled ligands are approximated by the known values of their total concentrations, since the free concentrations are not easily determined. Although equations have been derived previously that give the exact solution with the free concentrations of unlabeled ligands treated as variables, these have not been useful in practice. We have devised a mathematical model for the competitive binding that which is both exact and practical for the general case of one labeled ligand, any number of unlabeled ligands, and any number of classes of binding sites. In this model, the total concentrations of unlabeled ligands are the explicit variables, instead of their free concentrations. The free concentrations of unlabeled ligands can be estimated from the model. The model is based on the law of mass action and the dilution principle, as well as a new concept, called the equivalent competitive binding principle.

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