Exploring group size for statistical analysis of real-time signalling experiments.

Abstract

Classical pharmacological bioassays generally use observed effects from a concentration series, at a single equilibrium time point to construct a concentration-effect curve, representing one experiment. However, if the full kinetic profile of the effect data for each concentration was evaluated simultaneously, then the analysis would be more powerful. In this work, we explore if more precise parameters can be achieved by using the full kinetic method. We used a simulation estimation study to explore the influence of kinetic analysis on the precision of the Emax model parameter estimates (Emax and C50 ). We compared a full kinetic approach in which all effect versus time data from a theoretical real-time signalling experiment were analysed simultaneously with a 'reference' approach. The theoretical real-time signalling experiment was based on a previously published CB2 receptor-binding experiment. The reference method with a group size (n) of 5 provided highly precise parameter estimates (coefficient of variation [CV] 3.4% for Emax and 0.72% for C50 ). A full kinetic method provided more precise estimates than the reference with equal or smaller group sizes. Note that group size 'n' here refers to the number of technical replicates rather than the number of biological replicates. A full kinetic method can yield more precise parameter estimates than the equilibrium method. Such an approach may be more useful for researchers.