Probing the interaction of thionine with human serum albumin by multispectroscopic studies and its <i>in vitro</i> cytotoxic activity toward MCF-7 breast cancer cells Perumal Manivel Manickam Paulpandi Kadarkarai Murugan Giovanni Benelli Malaichamy Ilanchelian 10.6084/m9.figshare.4091502.v1 https://tandf.figshare.com/articles/dataset/Probing_the_interaction_of_thionine_with_human_serum_albumin_by_multispectroscopic_studies_and_its_i_in_vitro_i_cytotoxic_activity_toward_MCF-7_breast_cancer_cells/4091502 <p>The studies on protein–dye interactions are important in biological process and it is regarded as vital step in rational drug design. The interaction of thionine (TH) with human serum albumin (HSA) was analyzed using isothermal titration calorimetry (ITC), spectroscopic, and molecular docking technique. The emission spectral titration of HSA with TH revealed the formation of HSA–TH complex <i>via</i> static quenching process. The results obtained from absorption, synchronous emission, circular dichroism, and three-dimensional (3D) emission spectral studies demonstrated that TH induces changes in the microenvironment and secondary structure of HSA. Results from ITC experiments suggested that the binding of TH dye was favored by negative enthalpy and a favorable entropy contribution. Site marker competitive binding experiments revealed that the binding site of TH was located in subdomain IIA (Sudlow site I) of HSA. Molecular docking study further substantiates that TH binds to the hydrophobic cavity of subdomain IIA (Sudlow site I) of HSA. Further, we have studied the cytotoxic activity of TH and TH–HSA complex on breast cancer cell lines (MCF-7) by MTT assay and LDH assay. These studies revealed that TH–HSA complex showed the higher level of cytotoxicity in cancer cells than TH dye-treated MCF-7 cells and the significant adverse effect did not found in the normal HBL-100 cells. Fluorescence microscopy analyses of nuclear fragmentation studies validate the significant reduction of viability of TH–HSA-treated human MCF-7 breast cancer cells through activation of apoptotic-mediated pathways.</p> 2016-10-27 07:12:05 human serum albumin thionine emission spectroscopy molecular docking MCF-7 breast cancer cells