A mathematical model for dynamics of CD40 clustering
Ligand bound-receptors in a signalosome complex trigger signals to determine cellular
functions. Upon ligand binding, the ligand–receptor complexes form clusters on cell
membrane. Guided by the previous experimental reports on the cluster formation of CD40, a
trans membrane receptor for CD40-ligand, we built a minimal model of the receptor cluster
formation. In this model, we studied co-operative and non-co-operative clustering of a
maximum of four CD40 molecules assuming a positive mediator of clustering such as …
functions. Upon ligand binding, the ligand–receptor complexes form clusters on cell
membrane. Guided by the previous experimental reports on the cluster formation of CD40, a
trans membrane receptor for CD40-ligand, we built a minimal model of the receptor cluster
formation. In this model, we studied co-operative and non-co-operative clustering of a
maximum of four CD40 molecules assuming a positive mediator of clustering such as …
Abstract
Ligand bound-receptors in a signalosome complex trigger signals to determine cellular functions. Upon ligand binding, the ligand–receptor complexes form clusters on cell membrane. Guided by the previous experimental reports on the cluster formation of CD40, a trans membrane receptor for CD40-ligand, we built a minimal model of the receptor cluster formation. In this model, we studied co-operative and non-co-operative clustering of a maximum of four CD40 molecules assuming a positive mediator of clustering such as cholesterol to be present in both cases. We observed that co-operative interactions between CD40 molecules resulted in more of the largest CD40 clusters than that observed with the non-co-operatively interacting CD40 molecules. We performed global sensitivity analysis on the model parameters and the analyses suggested that cholesterol influenced only the initial stage of the co-operatively clustering CD40 molecules but it affects both the initial and the final stages in case of the non-co-operatively clustering CD40 molecules. Robustness analyses revealed that in both co-operative and non-co-operative interactions, the higher order clusters beyond a critical size are more robust with respect to alterations in the environmental parameters including the cholesterol. Thus, the role of co-operative and non-co-operative interactions in environment-influenced receptor clustering is reported for the first time.
Springer
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