Key result
The binding of the first, third, and fourth cAMP ligand evoked robust HCN2 channel opening, whereas the second ligand obstructed opening, revealing pronounced hysteresis for activation and deactivation.
The study provides quantitative insight into the complex interaction of the four structurally equal subunits of HCN2 channels, demonstrating pronounced hysteresis for activation and deactivation.
Does not support clinical translation; leaves open quantitative models of HCN2 subunit hysteresis for future arrhythmia research.
Hyperpolarization-activated cyclic nucleotide-modulated (HCN) channels are voltage-gated tetrameric cation channels that generate electrical rhythmicity in neurons and cardiomyocytes. Activation can be enhanced by the binding of adenosine-3',5'-cyclic monophosphate (cAMP) to an intracellular cyclic nucleotide binding domain. Based on previously determined rate constants for a complex Markovian model describing the gating of homotetrameric HCN2 channels, we analyzed probability fluxes within this model, including unidirectional probability fluxes and the probability flux along transition paths. The time-dependent probability fluxes quantify the contributions of all 13 transitions of the model to channel activation. The binding of the first, third and fourth ligand evoked robust channel opening whereas the binding of the second ligand obstructed channel opening similar to the empty channel. Analysis of the net probability fluxes in terms of the transition path theory revealed pronounced hysteresis for channel activation and deactivation. These results provide quantitative insight into the complex interaction of the four structurally equal subunits, leading to non-equality in their function.
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Benndorf et al. (2012) studied HCN2 channel gating. cAMP (ligand) vs. 0 mM (ligand removal) was evaluated on Probability fluxes and transition paths in channel activation and deactivation. The binding of the first, third, and fourth cAMP ligand evoked robust HCN2 channel opening, whereas the second ligand obstructed opening, revealing pronounced hysteresis for activation and deactivation.
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