Carboxylate−Imidazole Cooperativity in Dipeptide-Functionalized Gold Nanoparticles with Esterase-like Activity
- 25 January 2005
- journal article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 127 (6) , 1616-1617
- https://doi.org/10.1021/ja043547c
Abstract
We report here the first example of peptide-functionalized gold nanoparticles hydrolytically active against carboxylate esters. The active units are constituted by His-Phe-OH terminating thiols. The confinement of the catalytic units in the monolayer covering the nanoparticles triggers a cooperative hydrolytic mechanism operative at pH < 7 in which a carboxylate and an imidazolium ion act as general base and general acid, respectively. Such a mechanism is absent with an analogous monomeric dipeptide, and this results in a more than 300-fold rate acceleration of the hydrolytic process at low pH in the presence of the functional nanoparticles.Keywords
This publication has 13 references indexed in Scilit:
- EPR Study of Dialkyl Nitroxides as Probes to Investigate the Exchange of Solutes between the Ligand Shell of Monolayers of Protected Gold Nanoparticles and Aqueous SolutionsJournal of the American Chemical Society, 2004
- Spontaneous assembly of subnanometre-ordered domains in the ligand shell of monolayer-protected nanoparticlesNature Materials, 2004
- Synthesis, characterization and properties of water-soluble gold nanoparticles with tunable core sizeJournal of Materials Chemistry, 2003
- Nanoparticles: Scaffolds and Building BlocksAccounts of Chemical Research, 2003
- Enzyme-like Catalysis by Molecularly Imprinted PolymersChemical Reviews, 2001
- Artificial EnzymesChemical Reviews, 1996
- Enzyme modelsRecueil des Travaux Chimiques des Pays-Bas, 1994
- Ion binding and reactivity at charged aqueous interfacesAccounts of Chemical Research, 1991
- Reaction of pyridoxal 5'-sulfate with apoenzyme of aspartate aminotransferase. Covalent labeling of the protein with elimination of sulfateBiochemistry, 1974
- Electronic Structure and Auxin Activity of Benzoic Acid DerivativesJournal of the American Chemical Society, 1958