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

被引:243
作者
Fujita, K
Katahira, J
Horiguchi, Y
Sonoda, N
Furuse, M
Tsukita, S
机构
[1] Kyoto Univ, Fac Med, Dept Cell Biol, Sakyo Ku, Kyoto 606, Japan
[2] Kyoto Univ, Fac Med, Dept Neurosurg, Sakyo Ku, Kyoto 6068501, Japan
[3] Osaka Univ, Microbial Dis Res Inst, Project Res Mol Bacteriol, Osaka 5650871, Japan
关键词
claudin; tight junction; tight junction strand; barrier; Clostridium perfringens enterotoxin;
D O I
10.1016/S0014-5793(00)01744-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
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页码:258 / 261
页数:4
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