4.5 Article

Clostridium perfringens enterotoxin binds to the second extracellular loop of claudin-3, a tight junction integral membrane protein

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FEBS LETTERS
卷 476, 期 3, 页码 258-261

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ELSEVIER SCIENCE BV
DOI: 10.1016/S0014-5793(00)01744-0

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claudin; tight junction; tight junction strand; barrier; Clostridium perfringens enterotoxin

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Claudins (claudin-1 to -18) with four transmembrane domains and two extracellular loops constitute tight junction strands. The peptide toxin Clostridium perfringens enterotoxin (CPE) has been shown to bind to claudin-3 and -4, but not to claudin-1 or -2, We constructed claudin-1/claudin-3 chimeric molecules and found that the second extracellular loop of claudin-3 conferred CPE sensitivity on L fibroblasts, Furthermore, overlay analyses revealed that the second extracellular loop of claudin-3 specifically bound to CPE at the K-a value of 1.0 X 10(8) M-1. We concluded that the second extracellular loop is the site through which claudin-3 interacts with CPE on the cell surface. (C) 2000 Federation of European Biochemical Societies. Published by Elsevier Science B.V. All rights reserved.

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