Dispersion interactions in fluorinated biopolymers

• Applicant: Dr. Ana Vila Verde, since 4/2019
• Subject Area: Statistical Physics, Nonlinear Dynamics, Complex Systems, Soft and Fluid Matter, Biological Physics ; Biological and Biomimetic Chemistry ; Physical Chemistry of Molecules, Liquids and Interfaces, Biophysical Chemistry ; Theoretical Chemistry: Electronic Structure, Dynamics, Simulation
• Term: from 2018 to 2021
• Project identifier: Deutsche Forschungsgemeinschaft (DFG) - Project number 398048621

The structure and function of biopolymers are determined by the balance of different types of interactions: electrostatic, dispersion, and hydrophobic interactions. The latter are important in understanding the “hydrophobic effect” associated with aggregation of apolar solutes in aqueous environment. Dispersion interactions thus play a major role in the biopolymer structure and dynamics, leading to and stabilizing protein assemblies. Fluorination has been shown to modulate the properties of small molecules by altering the balance between electrostatic and dispersion interactions. Similar effects can be expected for peptides, proteins and other biopolymers. To explore the impact of fluorination on hydrated biopolymers, we will employ molecular simulations at atomic level detail, in comparison with Raman experiments provided by our collaboration partners. First principles simulations of fluorinated and non-fluorinated small molecules in gas phase and in solution will allow us to dissect the balance of electrostatic and dispersive interactions on an electronic structure level. These calculations will furthermore serve as reference data for the development of classical force field parameters. Using these parameters, classical molecular dynamics simulations on a larger scale will reveal the impact of fluorination on the dispersion interactions in biopolymers and their dependence on polymer length, conformation, and structural flexibility. These aspects, which are important for proteins, cannot be studied in the very small molecules typically used as analogues of amino acid side chains. However, direct dispersive interactions between hydrophobic groups in solution do depend on the distance of these groups and thus the shape and conformational dynamics of the polymer. Our simulations of selectively fluorinated biopolymers will probe whether dispersion interactions are the dominant contribution to hydrophobic attraction and may thus account for changes in protein structure and structural stability in fluorinated proteins. This understanding can ultimately be used to modify the balance of the different interactions and thereby control protein properties via specific fluor-substitution.

• DFG Programme: Priority Programmes
• Subproject of: SPP 1807: Control of London Dispersion Interactions in Molecular Chemistry
• International Connection: USA
• Co-Investigators: Professor Dr. Markus Gerhards (†); Professorin Dr. Beate Koksch
• Cooperation Partner: Professor Dor Ben-Amotz, Ph.D.
• Ehemalige Antragstellerin: Professorin Dr. Petra Imhof, until 3/2019