Description of a non-competitive ELISA based on time course analysis of ligand binding at saturation, and a direct method for calculating the affinity of monoclonal antibodies.

We present a time-course saturation ELISA for measuring the equilibrium constant of the monoclonal antibody (mAb) SIM 28 against horse radish peroxidase (HRP). The curves of HRP binding to a series of fixed mAb dilutions were plotted to completion, and the K (= K) value (time to occupy 50 % of the mAb paratopes) was determined for each mAb dilution and HRP concentration. Analysis of the kinetic mechanism of the reaction by Lineweaver-Burk and Hanes plots showed that the slope and y-intercept were affected, indicating that mAb ligand saturation follows non-competitive inhibition kinetics in this assay format. In this kinetics, the inhibition constant K (= K) is the time required to double the slope or halve the V of the Lineweaver-Burk plot. The K values of the time courses were doubled (2 x K) and normalized by dividing by the total reaction time to obtain a unitless factor which, when multiplied by the concentration of HRP, gives the K. The affinity constant of mAb SIM 28 was determined from ELISA data (n = 16) by three methods: i) doubling of K, ii) Beatty equation (K = (n-1)/2 (n [HRP'] - [HRP]), and iii) SPR (Biacore) analysis. The calculated affinities (mean ± 95 % confidence limits) were i) 4.6 ± 0.67 × 10 M, ii) K = 0.23 ± 0.03 × 10 M (K = 4.8 ± 0.81 × 10 M), and iii) 4.3 ± 0.57 × 10 M, respectively. The similar results obtained with the three different techniques indicate that this time-course saturation ELISA, combined with the double K method, is a repeatable and direct approach to mAb affinity determination.