Wydział Chemii

Agnieszka Kadej

Mariola Kuczer

Teresa Kowalik-Jankowska

2015

Dalton Transactions

44

20659-20674

10.1039/c5dt01911g

Naukowa

Angielski

Artykuł

Mononuclear and polynuclear copper(II) complexes of alloferon 1 with point mutations, H1A/H12A H₂N-A¹GVSGH⁶GQH⁹GVA¹²G-COOH, H1A/H9A H₂N-A¹GVSGH⁶GQA⁹GVH¹²G-COOH, and H1A/H6A H₂N-A¹GVSGA⁶GQH⁹GVH¹²G-COOH, have been studied by potentiometric, UV-visible, CD, and EPR spectroscopy, and mass spectrometry (MS) methods. Complete complex speciation at different metal-to-ligand molar ratios ranging from 1 : 1 to 3 : 1 was obtained. Over a wide 6–8 pH range, including physiological pH 7.4, and a 1 : 1 metal-to-ligand molar ratio, the peptides studied formed a CuH₋₁L complex with the 4N{NH₂,N⁻,2N_Im} coordination mode. The presence of the 4N binding site for the CuH₋₁L complexes prevented the deprotonation and coordination of the second amide nitrogen atom to copper(II) ions (pK_−1/−2 7.83–8.07) compared to that of pentaGly (6.81). The amine nitrogen donor and two imidazole nitrogen atoms (H⁶H⁹, H⁶H¹² and H⁹H¹²) can be considered to be independent metal-binding sites in the species formed. As a consequence, di- and trinuclear complexes for the metal-to-ligand 2 : 1 and 3 : 1 molar ratios dominate in the solution, respectively. For the Cu(II)-H1A/H9A and Cu(II)-H1A/H12A systems, the Cu₃H₋₉L complexes are likely formed by the coordination of amide nitrogen atoms towards C-termini with ring sizes (7,5,5).

http://dx.doi.org/10.1039/c5dt01911g

https://www.rsc.org/