Details

Autor(en) / Beteiligte

• Zanetti-Polzi, Laura
• Corni, Stefano
• Daidone, Isabella
• Amadei, Andrea

Titel

Extending the essential dynamics analysis to investigate molecular properties: application to the redox potential of proteinsElectronic supplementary information (ESI) available: Additional analysis on the two azurin mutants Mut1 and Mut2. See DOI: 10.1039/c6cp03394f

Erscheinungsjahr

2016-07

Quelle

Alma/SFX Local Collection

Beschreibungen/Notizen

• Here, a methodology is proposed to investigate the collective fluctuation modes of an arbitrary set of observables, maximally contributing to the fluctuation of another functionally relevant observable. The methodology, based on the analysis of fully classical molecular dynamics (MD) simulations, exploits the essential dynamics (ED) method, originally developed to analyse the collective motions in proteins. We apply this methodology to identify the residues that are more relevant for determining the reduction potential ( E 0 ) of a redox-active protein. To this aim, the fluctuation modes of the single-residue electrostatic potentials mostly contributing to the fluctuations of the total electrostatic potential (the main determinant of E 0 ) are investigated for wild-type azurin and two of its mutants with a higher E 0 . By comparing the results here obtained with a previous study on the same systems [Zanetti-Polzi et al. , Org. Biomol. Chem. , 2015, 13 , 11003] we show that the proposed methodology is able to identify the key sites that determine E 0 . This information can be used for a general deeper understanding of the molecular mechanisms on the basis of the redox properties of the proteins under investigation, as well as for the rational design of mutants with a higher or lower E 0 . From the results of the present analysis we propose a new azurin mutant that, according to our calculations, shows a further increase of E 0 . An extension of the essential dynamics analysis is applied to investigate the collective fluctuation modes of the single-residue electrostatic potentials that determine the redox potential of azurin.