CuII ion coordination to an unprotected pentadecapeptide containing two His residues:: Competition between the terminal amino and the side-chain imidazole nitrogen donors

被引:10
作者
Conato, C
Kamysz, W
Kozlowski, H
Luczkowski, M
Mackiewicz, Z
Mancini, F
Mlynarz, P
Remelli, M
Valensin, D
Valensin, G
机构
[1] Univ Ferrara, Dipartmento Chim, I-44100 Ferrara, Italy
[2] Univ Gdansk, Fac Chem, PL-80952 Gdansk, Poland
[3] Univ Wroclaw, Fac Chem, PL-50383 Wroclaw, Poland
[4] Univ Siena, Dept Chem, I-53100 Siena, Italy
关键词
copper; peptides; coordination chemistry; bioinorganic chemistry;
D O I
10.1002/ejic.200200551
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The complex-formation equilibria of the pentadecapeptide TLEGTKKGHKLHLDY, the 114-128 protein fragment of SPARC, with the Cull ion have been investigated, at I = 0.1 mol.dm(-3) (KNO3) and T = 298.2 K. Protonation and complex-formation constants have been determined potentiometrically, and formation enthalpies measured by direct solution calorimetry; the complex-formation model and species stoichiometry have been carefully checked by means of UV/Vis absorption, CD and EPR spectroscopy. The structure hypo-theses of the complex species are also based on detailed study of the H-1 and C-13 NMR spectra of the ligand in both the absence and presence of copper ions. The involvement in complex-formation of both the terminal amino and imidazole groups has been suggested and their specific behaviour at different pH values elucidated. ((C) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003).
引用
收藏
页码:1694 / 1702
页数:9
相关论文
共 30 条
[1]   How non-bonding amino acid side-chains may enormously increase the stability of a Cu(II)-peptide complex [J].
Bal, W ;
Dyba, M ;
Kasprzykowski, F ;
Kozlowski, H ;
Latajka, R ;
Lankiewicz, L ;
Mackiewicz, Z ;
Pettit, LD .
INORGANICA CHIMICA ACTA, 1998, 283 (01) :1-11
[2]  
Barany G., 1980, PEPTIDES, P1
[3]   Matricellular proteins: an overview - Introduction [J].
Bornstein, P .
MATRIX BIOLOGY, 2000, 19 (07) :555-556
[4]   SPARC, a matricellular protein that functions in cellular differentiation and tissue response to injury [J].
Bradshaw, AD ;
Sage, EH .
JOURNAL OF CLINICAL INVESTIGATION, 2001, 107 (09) :1049-1054
[5]   SPARC, a matricellular protein: at the crossroads of cell-matrix [J].
Brekken, RA ;
Sage, EH .
MATRIX BIOLOGY, 2000, 19 (07) :569-580
[6]   Cu(II) ion coordination to the pentadecapeptide model of the SPARC copper-binding site [J].
Conato, C ;
Kamysz, W ;
Kozlowski, H ;
Luczkowski, M ;
Mackiewicz, Z ;
Mlynarz, P ;
Remelli, M ;
Valensin, D ;
Valensin, G .
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 2002, (21) :3939-3944
[7]   Copper complexes of glycyl-histidyl-lysine and two of its synthetic analogues: chemical behaviour and biological activity [J].
Conato, C ;
Gavioli, R ;
Guerrini, R ;
Kozlowski, H ;
Mlynarz, P ;
Pasti, C ;
Pulidori, F ;
Remelli, M .
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 2001, 1526 (02) :199-210
[8]   Ultraviolet-circular dichroism spectra for structural analysis of copper(II) complexes with aliphatic and aromatic ligands in aqueous solution [J].
Daniele, PG ;
Prenesti, E ;
Ostacoli, G .
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 1996, (15) :3269-3275
[9]   Crystal structure of a pair of follistatin-like and EF-hand calcium-binding domains in BM-40 [J].
Hohenester, E ;
Maurer, P ;
Timpl, R .
EMBO JOURNAL, 1997, 16 (13) :3778-3786
[10]  
*HYP INC, 1997, HYPERCHEM HYP REL 5