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Nature Methods , 227<br />
230, 2007<br />
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PNAS , 1347513480, 2009<br />
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PLoS ONE , e21531, 2011<br />
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Tight junctions prevent the leakage of solutes through the paracellular<br />
pathway of epithelial cells and are indispensable in establishing the<br />
various compositionally distinct fluid compartments within the body<br />
of multicellular organisms.<br />
Based on morphological observations, two models about the tight<br />
junction have been proposed. The protein model proposes that a<br />
linear array of membrane protein particles polymerize to form a tight<br />
junction strand and that a network of these strands adhere with paired<br />
strands from apposing cells to obliterate the intercellular space. On<br />
the other hand, the lipid model, which originates from the observation<br />
of exoplasmic lipid leaflet fusion, proposes that the fusion of these<br />
lipid leaflets is associated with a transformation of the lamellar phase<br />
of the lipid bilayers into a non-lamellar, inverted micelle structure at<br />
tight junctions.<br />
Much has been learned about the membrane proteins at tight junctions<br />
over the last decade. However, how these membrane proteins function<br />
as the barriers in the paracellular space remains to be elucidated.<br />
Here, I will present recent progress toward a better understanding of<br />
supra-molecular complex at tight junctions.