Journal
JOURNAL OF COMPUTER-AIDED MOLECULAR DESIGN
Volume 36, Issue 1, Pages 11-24Publisher
SPRINGER
DOI: 10.1007/s10822-021-00434-1
Keywords
GPCR; Protein-ligand interaction; Binding site prediction; Protein structure
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Funding
- European Research Council Synergy grant ASTRA [855923]
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This study proposes a new computational approach based on Zernike polynomials for identifying binding sites of specific ligands on GPCRs. By analyzing the shape complementarity of local molecular surfaces, the method can distinguish binding pockets from randomly sampled regions on the receptor surface. The method achieves an Area Under ROC curve of 0.77 in experiments, demonstrating its ability for rapid and efficient screening of potential drugs.
Studying the binding processes of G protein-coupled receptors (GPCRs) proteins is of particular interest both to better understand the molecular mechanisms that regulate the signaling between the extracellular and intracellular environment and for drug design purposes. In this study, we propose a new computational approach for the identification of the binding site for a specific ligand on a GPCR. The method is based on the Zernike polynomials and performs the ligand-GPCR association through a shape complementarity analysis of the local molecular surfaces. The method is parameter-free and it can distinguish, working on hundreds of experimentally GPCR-ligand complexes, binding pockets from randomly sampled regions on the receptor surface, obtaining an Area Under ROC curve of 0.77. Given its importance both as a model organism and in terms of applications, we thus investigated the olfactory receptors of the C. elegans, building a list of associations between 21 GPCRs belonging to its olfactory neurons and a set of possible ligands. Thus, we can not only carry out rapid and efficient screenings of drugs proposed for GPCRs, key targets in many pathologies, but also we laid the groundwork for computational mutagenesis processes, aimed at increasing or decreasing the binding affinity between ligands and receptors.
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