A Kinetic Model for Type I and II IP3R Accounting for Mode Changes

Abstract

Based upon an extensive single-channel data set, a Markov model for types I and II inositol trisphosphate receptors (IP3R) is developed. The model aims to represent accurately the kinetics of both receptor types of IP3R depending on the concentrations of inositol trisphosphate (IP3), adenosine trisphosphate (ATP), and intracellular calcium (Ca2+). In particular, the model takes into account that for some combinations of ligands the IP3R switches between extended periods of inactivity alternating with intervals of bursting activity (mode changes). In a first step, the inactive and active modes are modeled separately. It is found that, within modes, both receptor types are ligand-independent. In a second step, the submodels are connected by transition rates. Ligand-dependent regulation of the channel activity is achieved by modulating these transitions between active and inactive modes. As a result, a compact representation of the IP3R is obtained that accurately captures stochastic single-channel dynamics including mode changes in a model with six states and 10 rate constants, only two of which are ligand-dependent.