Obiettivo
Due to its fundamental regulatory role, molecular recognition has been extensively studied by both experiments and
simulations. During the last 30 years impressive technical advances allowed significant progress in understanding molecular
recognition mechanisms. However, the matter is far from settled and contradictory reports are still appearing in the literature.
Lately, I have been studying these processes using a combination of computational and experimental approaches in
different systems. Here I propose to study several representative model systems in great details, taking advantages of new force fields, DFT functionals and enhanced sampling algorithms recently emerged. These systems are small enough to allow the use of state-of-the-art simulation techniques; still they are sufficiently complex not only to mimic the behaviour of far larger systems but also to use apparently different mechanisms. Indeed, their molecular recognition needs complex conformational changes, the re-arrangement
of water molecules in the binding cavity, and an active role of the ligand in the binding/release mechanisms. The overarching
objective of my proposal is to learn the state-of-the-art enhanced sampling techniques developed at UCL and combine them
with QM/MM approaches to: i) understand how bio-molecular recognition works in both isoforms, ii) fully characterize the
thermodynamics and kinetic processes that govern them and iii) validate the computational approaches against high-quality
experimental data. If successful, the in-depth understanding of the molecular binding mechanism will shed light on an
intriguing and important biological system and provide a much needed benchmark to the computational community. This
challenging but feasible project will have a far reaching impact on a number of H2020 priority areas, including drug discovery
and bio-molecular engineering.
Campo scientifico (EuroSciVoc)
CORDIS classifica i progetti con EuroSciVoc, una tassonomia multilingue dei campi scientifici, attraverso un processo semi-automatico basato su tecniche NLP.
CORDIS classifica i progetti con EuroSciVoc, una tassonomia multilingue dei campi scientifici, attraverso un processo semi-automatico basato su tecniche NLP.
- scienze mediche e della salutemedicina di basefarmacologia e farmaciascoperta di farmaci
- scienze naturaliscienze fisichetermodinamica
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Programma(i)
Argomento(i)
Meccanismo di finanziamento
MSCA-IF-EF-ST - Standard EFCoordinatore
WC1E 6BT London
Regno Unito