Multi-scale modeling of cardiac signaling networks

Since the first model of the cardiac myocyte in 1960, integration of models and experiments has been crucial for understanding heart function. While these models have primarily focused on electrophysiology and excitation-contraction coupling, we have recently developed the first mechanistic models of cardiac signaling networks and their integration with cardiac physiology. In this talk, I will describe the use of models of the beta-adrenergic signaling network to address biological questions at multiple functional and spatial scales. These include identifying new functional roles for proteins, clinically-relevant consequences of a gene mutation, and how biochemical signals are amplified to strengthen heart contractions during stress.