Kinetic and thermodynamic studies of the copper (II) and nickel(II) complexes of glycylglycyl-L-histidine

J Inorg Biochem. 1993 Oct 1;52(1):17-25. doi: 10.1016/0162-0134(93)85619-j.

Abstract

The protonation constants of the tripeptide glycylglycyl-L-histidine (L-) have been determined at 25 degrees C and I = 0.1 mol dm-3 as log K 8.06, 6.82, and 2.80. Complexation with copper(II) can be represented by the series of equilibria [formula: see text] in the case of nickel(II) only the species [NiLH]2+, [NiL]+, and [NiLH-2]- are of importance with log beta 111 = 11.33(2); log beta 110 = 4.74(6), and log beta 11-2 = -6.93(1). The tripeptide acts as a quadridentate ligand to give complexes with copper and nickel with an amino group, two deprotonated amide groups and an imidazole pyridine nitrogen (Im-N3) as donors. At 1:1 ligand-to-metal ratios the purple copper(II) complex [CuLH-2]- is essentially 100% abundant above pH 7 and the planar yellow [NiLH-2]- above pH 8. The displacement of the tripeptide ligand from the nickel(II) complex by L-histidine has been studied kinetically over the pH range 7-8. There is a small solvolytic reaction and a reaction which is first-order in the hydrogen ion concentration. Under the experimental conditions employed, the reaction is essentially independent of the L-His concentration and displacement occurs by a proton-assisted nucleophilic pathway with rate-determining cleavage of the first nickel(II)-N(peptide) bond.

MeSH terms

  • Amino Acid Sequence
  • Copper / chemistry*
  • Kinetics
  • Molecular Sequence Data
  • Nickel / chemistry*
  • Oligopeptides / chemistry*
  • Solutions
  • Spectrophotometry
  • Thermodynamics*

Substances

  • Oligopeptides
  • Solutions
  • diglycyl-histidine
  • Copper
  • Nickel