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Membrane transporters are critical modulators of drug pharmacokinetics, efficacy, and safety. One example is the proton-dependent oligopeptide transporter PepT1, also known as SLC15A1, which is responsible for the uptake of the ?-lactam antibiotics and various peptide-based prodrugs. In this study, we modeled the binding of various peptides to a bacterial homolog, PepT(St), and evaluated a range of computational methods for predicting the free energy of binding. Our results show that a hybrid approach (endpoint methods to classify peptides into good and poor binders and a theoretically exact method for refinement) is able to accurately predict affinities, which we validated using proteoliposome transport assays. Applying the method to a homology model of PepT1 suggests that the approach requires a high-quality structure to be accurate. Our study provides a blueprint for extending these computational methodologies to other pharmaceutically important transporter families.

Original publication

DOI

10.1016/j.chembiol.2015.11.015

Type

Journal article

Journal

Cell Chem Biol

Publication Date

18/02/2016

Volume

23

Pages

299 - 309

Keywords

Anti-Bacterial Agents, Humans, Ligands, Molecular Dynamics Simulation, Oligopeptides, Prodrugs, Symporters, Thermodynamics