Exploring the interaction of phenothiazinium dyes methylene blue, new methylene blue, azure A and azure B with tRNAPhe: spectroscopic, thermodynamic, voltammetric and molecular modeling approach. Issue 9 (17th February 2017)

• Record Type: Journal Article
• Authors: Paul, Puja; Mati, Soumya Sundar; Bhattacharya, Subhash Chandra; Kumar, Gopinatha Suresh
• Is Part Of: Physical chemistry chemical physics. Volume 19:Issue 9(2017)
• Page Start: 6636
• Page End: 6653
• Publication Date: 2017-02-17
• Subjects: Chemistry, Physical and theoretical -- Periodicals; 541.3
• DOI: 10.1039/c6cp07888e
• Languages: English
• ISSNs: 1463-9076

Abstract

Abstract : RNA targeting by small molecules. Abstract : This study focuses on the understanding of the interaction of phenothiazinium dyes methylene blue (MB), new methylene blue (NMB), azure A (AZA) and azure B (AZB) with tRNA Phe with particular emphasis on deciphering the mode and energetics of the binding. Strong intercalative binding to tRNA Phe was observed for MB, NMB and AZB, bound by a partial intercalative mode. AZA has shown groove binding characteristics. From spectroscopic studies binding affinity values of the order of 10 5 M −1 were deduced for these dyes; the trend varied as MB > NMB > AZB > AZA. The binding was characterized by an increase of thermal melting temperatures and perturbation in the circular dichroism spectrum of tRNA. All the dyes acquired optical activity upon binding to tRNA. The binding was predominantly entropy driven with a favorable enthalpy term that increased with temperature in all the cases. Dissection of the Gibbs energy to polyelectrolytic and non-polyelectrolytic terms revealed a major role of the non-electrostatic forces in the binding. The small but significant heat capacity changes and the observed enthalpy–entropy compensation phenomenon confirmed the involvement of multiple weak non-covalent forces driving the interaction. The mode of binding was confirmed from quenching, viscosity and cyclic voltammetric results. Using density functional theory, ground state optimized structures of the dyes were calculated to provide insight into theoretical docking studies to correlate the experimental approaches. The modeling results verified the binding location as well as the binding energy of complexation. The results may provide new insights into the structure–activity relationship useful in the design of effective RNA targeted therapeutic agents.