bioRxiv2021
Computational methods play a pivotal role in drug discovery and are widely applied in virtual screening, structure optimization, and compound activity profiling. Over the last decades, almost all the attention in medicinal chemistry has been directed to protein-ligand binding, and computational tools have been created with this target in mind. With novel discoveries of functional RNAs and their possible applications, RNAs have gained considerable attention as potential drug targets. However, the availability of bioinformatics tools for nucleic acids is limited. Here, we introduce fingeRNAt - a software tool for detecting non-covalent interactions formed in complexes of nucleic acids with ligands. The program detects nine types of interactions: (i) hydrogen and (ii) halogen bonds, (iii) cation-anion, (iv) pi-cation, (v) pi-anion, (vi) pi-stacking, (vii) inorganic ion-mediated, (viii) water-mediated, and (ix) lipophilic interactions. However, the scope of detected interactions can be easily expanded using a simple plugin system. In addition, detected interactions can be visualized using the associated PyMOL plugin, which facilitates the analysis of medium-throughput molecular complexes. Interactions are also encoded and stored as a bioinformatics-friendly Structural Interaction Fingerprint (SIFt) - a binary string where the respective bit in the fingerprint is set to 1 if a particular interaction is present and to 0 otherwise. This output format, in turn, enables high-throughput analysis of interaction data using data analysis techniques. We present applications of fingeRNAt-generated interaction fingerprints for visual and computational analysis of RNA-ligand complexes, including analysis of interactions formed in experimentally determined RNA-small molecule ligand complexes deposited in the Protein Data Bank. We propose interaction-based similarity based on fingerprints as an alternative measure to RMSD to recapitulate complexes with similar interactions but different folding. We present an application of molecular fingerprints for the clustering of molecular complexes. This approach can be used to group ligands that form similar binding networks and thus have similar biological properties. AUTHOR SUMMARYWe present a novel bioinformatic tool, fingeRNAt, aiming to support scientists in the analysis of complexes of nucleic acids with various types of ligands. The software automatically detects non-covalent interactions and presents them in a form that is understandable to both humans and computers. Such data can help decipher the nature of interactions between nucleic acids and ligands and determine the main factors responsible for forming such complexes in nature. fingeRNAt finds application in multiple studies, both structure- and drug discovery-oriented. Here, we analyzed the experimentally solved structures of RNA complexes with small molecules to determine which binding features are most prevalent, i.e., most common interactions or their hot spots. The results of this analysis may help elucidate the mechanisms of binding and design new active molecules. Moreover, we propose to use the data generated by our software as a new metric for the quantitative comparison of two molecule complexes. We have shown that it is more reliable than the currently used methods in certain "difficult" cases. We have shown that the results of our program can be used for high-throughput analysis of molecular complexes and the search for active molecules. We are confident that fingeRNAt will be a valuable tool for exploring the complex world of interactions of nucleic acids with ligands.