On the different sources of cooperativity in pH titrating sites of a membrane protein channel

被引:3
作者
Alcaraz, Antonio [1 ]
Queralt-Martin, Maria [1 ]
机构
[1] Univ Jaume 1, Dept Phys, Lab Mol Biophys, Castellon de La Plana 12080, Spain
关键词
INTRAMOLECULAR INTERACTIONS; OMPF CHANNEL; SELECTIVITY; PORIN; BINDING; BLOCK;
D O I
10.1140/epje/i2016-16029-2
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Cooperative interactions play a central role in the regulation of protein functions. Here we show that in multi-site systems like ion channels the application of the Hill formalism could require a combination of different experiments, even involving site-directed mutagenesis, to identify the different sources of cooperativity and to discriminate between genuine and apparent cooperativity. We discuss the implications for the channel function in the bacterial porins PorA (N. meningitidis) and OmpF (E. coli) and the viroporin SARS-CoV E.
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页数:6
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