The epithelial and endothelial tissues serve as the physiological barriers against chemical and biological insurgents by constituting the tight junctions. Tight junctions are specialized adhesion constructs formed by the assembly of claudin family proteins. Membrane-embedded claudin proteins are the functional determinants of the tight junctions. In the paracellular space between two adjacent cells, claudins form size and charge-selective pores that impede free diffusion of these solutes. The vital role of tight junctions in various tissue barriers such as the blood-brain barrier, renal barrier, and gut barrier, etc. are currently active fields of research, yet a complete molecular understanding of the tight junctions is elusive. Here we have employed multiscale molecular dynamics simulations to gain insight into the underpinnings of claudin assembly at the tight junctions. From these simulations, a clear picture of how the membrane milieu influences the tight junction’s assembly is evident. Both cholesterol and ceramide lipids limit claudin-claudin interaction in the lipid bilayer, due to the reduced fluidity. Further, we were able to demonstrate that claudins preferentially assemble into distinct dimers that are the primary building blocks of the paracellular pores. The molecular-level insights gained from this work are critical in unraveling the physiological roles of tight junctions.<br/>

Molecular perspective on protein-protein interactions at the tight junctions interface

256th National Meeting (2018)

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