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  • Title: Copper(II) coordination properties of decapeptides containing three His residues: the impact of cyclization and Asp residue coordination.
    Author: Fragoso A, Delgado R, Iranzo O.
    Journal: Dalton Trans; 2013 May 07; 42(17):6182-92. PubMed ID: 23529654.
    Abstract:
    Two decapeptides containing three His and two Pro-Gly β-turn inducer units (C-Asn, cyclic) and three His and a single Pro-Gly unit (O-Asn, open) have been synthesized. A detailed potentiometric study showed that while O-Asn binds up to 3 equiv. of Cu(2+) ions, C-Asn only coordinates two before precipitation occurred. Nonetheless, at a 1 : 1 Cu(2+)/peptide ratio both peptides form a major [CuHL](3+) species and spectroscopic studies (UV-Vis, CD and EPR) revealed a very similar copper(ii) complex where the metal ion is coordinated solely by the imidazole rings of the His residues adopting a square planar or square pyramidal geometry. The corrected stability constants of the protonated species (log K(CuH(O-Asn)) = 8.17 and log K(CuH(C-Asn)) = 9.11) indicate that the cyclic peptide binds Cu(2+) with higher affinity and this value represents the highest value reported so far for this type of coordination. Additionally, the calculated value of the effective stability constant, K(eff), showed that C-Asn has a higher affinity for Cu(2+) at all pH values not only at a 1 : 1 ratio but even at a 2 : 1 ratio. The replacement of the asparagine residue by an aspartic amino acid increases the Cu(2+) affinity of the aspartic counterparts, C-Asp and O-Asp, which at a 1 : 1 Cu(2+)/peptide ratio also form a major species, [CuHL](2+) in these cases, with Cu(2+) coordinated to the three histidine residues and one aspartic residue. These data show how cyclization and coordination to the aspartic residue increase the binding strength and preclude the coordination of the amide nitrogen up to higher pH values, stabilizing therefore, the species where Cu(2+) is solely coordinated by the side chain functionalities.
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