The interaction between several L-amino acids and dipeptides and the ZnII complex with ligand L, a macrocycle containing a triamine chain linking the 2,9 positions of a phenanthroline moiety, has been studied by means of potentiometric and 1H NMR spectroscopic measurements in aqueous solutions. In the [ZnL]2+ complex, the metal ion displays an unsaturated coordination environment and the metal can act as a binding site for these substrates. Amino acids and dipeptides in their neutral (zwitterionic) form bind to ZnII through the carboxylate function and, when in their anionic form, through the amine group. In this case the carbonyl of the amide function is probably also involved in metal coordination. Amino acids containing aromatic pendants form the most stable complexes, due to hydrophobic and/or π-stacking interactions between the aromatic subunits of the substrates and the phenanthroline moiety of the metal receptor. The hydrolytic properties of the ZnII complex with L, involving the cleavage of the peptide bond, have been tested by using L-leucine-p-nitroanilide (LNA), which contains an activated peptide bond. This substrate forms stable [ZnL(LNA)]2+ and [ZnL(OH)(LNA)]+ complexes. The formation of the [ZnL(OH)(LNA)]+ complex is followed by LNA hydrolysis, through a nucleophilic attack of the Zn-OH function on the peptide bond.
Zn(II) complex with a phenanthroline-containig macrocycle as receptor for amino acids and dipeptides- Hydrolysis of an activated peptide bond / C. BAZZICALUPI; A. BENCINI; E. BERNI; A. BIANCHI; P. FORNASARI; C. GIORGI; B. VALTANCOLI. - In: EUROPEAN JOURNAL OF INORGANIC CHEMISTRY. - ISSN 1434-1948. - STAMPA. - ...:(2003), pp. 1974-1983. [10.1002/ejic.200200648]
Zn(II) complex with a phenanthroline-containig macrocycle as receptor for amino acids and dipeptides- Hydrolysis of an activated peptide bond
BAZZICALUPI, CARLA;BENCINI, ANDREA
;BIANCHI, ANTONIO
;GIORGI, CLAUDIA;VALTANCOLI, BARBARA
2003
Abstract
The interaction between several L-amino acids and dipeptides and the ZnII complex with ligand L, a macrocycle containing a triamine chain linking the 2,9 positions of a phenanthroline moiety, has been studied by means of potentiometric and 1H NMR spectroscopic measurements in aqueous solutions. In the [ZnL]2+ complex, the metal ion displays an unsaturated coordination environment and the metal can act as a binding site for these substrates. Amino acids and dipeptides in their neutral (zwitterionic) form bind to ZnII through the carboxylate function and, when in their anionic form, through the amine group. In this case the carbonyl of the amide function is probably also involved in metal coordination. Amino acids containing aromatic pendants form the most stable complexes, due to hydrophobic and/or π-stacking interactions between the aromatic subunits of the substrates and the phenanthroline moiety of the metal receptor. The hydrolytic properties of the ZnII complex with L, involving the cleavage of the peptide bond, have been tested by using L-leucine-p-nitroanilide (LNA), which contains an activated peptide bond. This substrate forms stable [ZnL(LNA)]2+ and [ZnL(OH)(LNA)]+ complexes. The formation of the [ZnL(OH)(LNA)]+ complex is followed by LNA hydrolysis, through a nucleophilic attack of the Zn-OH function on the peptide bond.File | Dimensione | Formato | |
---|---|---|---|
EJIC-aminoacids.pdf
Accesso chiuso
Descrizione: lavoro pubblicato
Tipologia:
Pdf editoriale (Version of record)
Licenza:
Tutti i diritti riservati
Dimensione
225.28 kB
Formato
Adobe PDF
|
225.28 kB | Adobe PDF | Richiedi una copia |
I documenti in FLORE sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.