Interactions between flavan-3-ols and poly(L-proline) studied by isothermal titration calorimetry: Effect of the tannin structure

被引:145
作者
Poncet-Legrand, Celine [1 ]
Gautier, Catherine
Cheynier, Veronique
Imberty, Anne
机构
[1] Univ Montpellier I, INRA, Montpellier SupAgro, UMR 1083 Sci Oenol, F-34000 Montpellier, France
[2] CERMAV, CNRS, Ctr Rech Macromol Vegetales, F-38041 Grenoble 9, France
[3] Univ Grenoble 1, F-38041 Grenoble, France
关键词
tannins; proline-rich proteins; titration microcalorimetry; interactions;
D O I
10.1021/jf071297o
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Interactions of proline-rich proteins (PRPs) with flavan-3-ols was studied using poly(L-proline) as a model protein by means of isothermal titration calorimetry (ITC). Several parameters were varied: (i) the galloylation and B-ring trihydroxylation of the flavan-3-ols (catechin, epicatechin, epicatechin gallate, and epigallocatechin gallate) and (ii) the degree of polymerization (monomers were compared to a mixture of oligomers with average degree of polymerization of 3.85). Large differences were observed between the flavan-3-ol monomers: no enthalpy change was measured when catechin and epicatechin were titrated by poly(L-proline), whereas thermodynamic parameters were determined in the case of galloylated monomers and mixture of oligomers. Stoichiometry ranged from 1 oligomer bound for each 12 proline units to 1 galloylated monomer for each 8 or 10 proline units. Association constants were in the range of 10(4)-10(5) M-1, indicating a relatively high affinity of galloylated flavanols toward poly(L-proline), and the coexistence of both enthalpy- and entropy-driven phenomena was suggested. Finally, the binding of grape seed tannins to proteins was shown to be a cooperative process.
引用
收藏
页码:9235 / 9240
页数:6
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