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Updated: Jul 13, 2026

Quantifying the Binding Interactions Between Cu(II) and Peptide Residues in the Presence and Absence of Chromophores
Published on: April 5, 2022
Optical spectra of Cu(II)-azurin by hybrid TDDFT-molecular dynamics simulations
Michele Cascella1, Michel A Cuendet, Ivano Tavernelli
1Laboratory of Computational Chemistry and Biochemistry, Ecole Polytechnique Fédérale de Lausanne (EPFL), FSB-ISIC-BCH 4109 1015, Lausanne, Switzerland.
Abstract:
The ground state electronic structure of oxidized azurin from Pseudomonas aeruginosa and its optical response have been investigated by combining hybrid quantum mechanics/molecular mechanics simulations with time-dependent density functional theory. In agreement with experiment, we find that the unpaired electron spin density is mainly localized on the copper ion. The vertical absorption spectrum in the visible range is well reproduced, with the central band centered around 2.1 eV. The anisotropic dipolar field due to the extended alpha-helix polarizes the metal binding site and is responsible for a shift of the absorption bands by +/-0.1-0.2 eV. At 300 K, the bond distances of the copper binding site undergo large fluctuations (approximately 0.3 A). It is crucial to take these thermal fluctuations into account for a faithful description of the optical properties.
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