Data di Pubblicazione:
2018
Abstract:
PDZ3 is an allosteric protein that represents an ideal test system to analyze
the molecular determinants at the basis of the allosteric mechanism. Recent computational
studies of the terahertz (THz) fluctuations of this protein have highlighted a response nucleus
for binding modulated by the ligand that is visible only at THz frequencies and that overlaps
with the known allosterically responding residues (Conti Nibali et al. 2017). With the aim
of further characterizing the changes in the terahertz dynamics of this allosteric protein
following the binding event, we have carried out an analysis of the correlation motions
of pairs of PDZ3 residues from molecular dynamic simulations. We identify concerted
and non-random THz fluctuations in the main secondary structure elements of the PDZ3.
Importantly, we highlight a concerted motion of some residues belonging to the allosteric
response nucleus for binding.
Tipologia CRIS:
14.a.1 Articolo su rivista
Keywords:
MD simulation; Protein dynamics; Dynamic allostery
Elenco autori:
CONTI NIBALI, Valeria; Morra, Giulia; Havenith, Martina; D'Angelo, Giovanna; Colombo, Giorgio
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