Selective control of Cu(II) complex stability in histidine peptides by β-alanine
| Autor: | Kamila Stokowa-Sołtys, Izabela Zawisza, Justyna Nagaj, Małgorzata Jeżowska-Bojczuk, Wojciech Bal, Arkadiusz Bonna |
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| Rok vydání: | 2013 |
| Předmět: |
Coordination sphere
Cations Divalent Protein Stability Chemistry Stereochemistry Circular Dichroism Cooperativity Biochemistry Inorganic Chemistry chemistry.chemical_compound Coordination Complexes Stability constants of complexes Amide Potentiometry beta-Alanine Side chain Imidazole Histidine Selectivity Oligopeptides Copper |
| Zdroj: | Journal of Inorganic Biochemistry. 119:85-89 |
| ISSN: | 0162-0134 |
| DOI: | 10.1016/j.jinorgbio.2012.11.002 |
| Popis: | The cooperativity of formation of 5-membered and 6-membered chelate rings is the driving force for specificity and selectivity in Cu(II) peptidic complexes. α-Amino acids enable the formation of 5-membered rings, while a 6-membered ring is provided by the coordination of the His side chain imidazole. Introduction of β-alanine is another way of creating a 6-membered ring in the Cu(II) complex. The potentiometric and spectroscopic (UV–vis and CD) study of Cu(II) complexation by a series of four peptides, AAH-am, ABH-am, BAH-am, and BBH-am (where B stands for β-alanine, and -am for C-terminal amide) revealed a very strong effect of the sizes of individual rings, with the order of complex stability AAH-am (5,5,6) > BAH-am (6,5,6) > ABH-am (5,6,6) ≫ BBH-am (6,6,6). The stabilities of ABH-am and BAH-am complexes are intermediate between those of strong His-3 peptides but these complexes are still able to saturate the coordination sphere of the Cu(II) ion at neutral pH. This fact opens up new possibilities in engineering specific peptide-based chelates. |
| Databáze: | OpenAIRE |
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