Complex formation and stability of westiellamide derivatives with copper(II)
The CuII coordination chemistry of three synthetic analogues of westiellamide (H3Lwa) with an [18]azacrown-6 macrocyclic structure and imidazole (H3L1), oxazole (H3L2), or thiazole (H3L3) heterocyclic donors in addition to the peptide groups, is reported. The Nheterocycle-Npeptide-Nheterocycle bindi...
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| Hauptverfasser: | , , , , , |
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| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
21 May 2010
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| In: |
Journal of biological inorganic chemistry
Year: 2010, Jahrgang: 15, Heft: 7, Pages: 1129-1135 |
| ISSN: | 1432-1327 |
| DOI: | 10.1007/s00775-010-0673-7 |
| Online-Zugang: | Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1007/s00775-010-0673-7
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| Verfasserangaben: | Peter Comba, Nina Dovalil, Gebhard Haberhauer, Graeme R. Hanson, Yuki Kato, Toshiaki Taura |
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| 520 | |a The CuII coordination chemistry of three synthetic analogues of westiellamide (H3Lwa) with an [18]azacrown-6 macrocyclic structure and imidazole (H3L1), oxazole (H3L2), or thiazole (H3L3) heterocyclic donors in addition to the peptide groups, is reported. The Nheterocycle-Npeptide-Nheterocycle binding sites are highly preorganized for the coordination to CuII ions. The stability constants of mono- and dinuclear CuII complexes of H3L1, H3L2, and H3L3, obtained by isothermal titration microcalorimetry, are reported. EPR and NMR spectroscopy as well as electrospray ionization mass spectrometry (ESI-MS) were used to characterize the complexes formed in solution. The stabilities of the mononuclear and dinuclear CuII complexes of the three ligands are in the range of 105 M−1, but there are subtle differences; specifically the oxazole-derived ligand has, in contrast to the other two macrocycles, a negative formation entropy for coordination to the first CuII ion and a higher stability for complexation to a second CuII center in comparison with the first CuII center (cooperativity). Differences between the three ligands are also apparent in terms of the formation mechanism. With the oxazole-based ligand H3L2, NMR spectroscopy, EPR spectroscopy, and ESI-MS indicate the formation of a ligand-CuII 2:1 intermediate, and this may explain the differences in the formation entropy as well as the cooperativity. | ||
| 650 | 4 | |a Complex formation | |
| 650 | 4 | |a Cyclic peptides | |
| 650 | 4 | |a Spectroscopy | |
| 650 | 4 | |a Stability constants | |
| 650 | 4 | |a Westiellamide | |
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| 700 | 1 | |a Hanson, Graeme R. |e VerfasserIn |4 aut | |
| 700 | 1 | |a Kato, Yuki |e VerfasserIn |4 aut | |
| 700 | 1 | |a Taura, Toshiaki |e VerfasserIn |4 aut | |
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