Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/8288
Full metadata record
DC FieldValueLanguage
dc.contributor.authorRoy, Swarupen_US
dc.contributor.authorSagdeo, Pankaj R.en_US
dc.contributor.authorKumar, Rajeshen_US
dc.date.accessioned2022-03-17T01:00:00Z-
dc.date.accessioned2022-03-21T11:16:01Z-
dc.date.available2022-03-17T01:00:00Z-
dc.date.available2022-03-21T11:16:01Z-
dc.date.issued2018-
dc.identifier.citationRoy, S., Saxena, S. K., Mishra, S., Yogi, P., Sagdeo, P. R., & Kumar, R. (2018). Spectroscopic evidence of phosphorous Heterocycle–DNA interaction and its verification by docking approach. Journal of Fluorescence, 28(1), 373-380. doi:10.1007/s10895-017-2199-7en_US
dc.identifier.issn1053-0509-
dc.identifier.otherEID(2-s2.0-85038120616)-
dc.identifier.urihttps://doi.org/10.1007/s10895-017-2199-7-
dc.identifier.urihttps://dspace.iiti.ac.in/handle/123456789/8288-
dc.description.abstractIn the present work, the interaction of phosphorous heterocycle (PH) with calf thymus DNA (CTDNA) has been studied using spectroscopy and verified by molecular modeling which is found to be in consonance with each other. Apparent association constant (Kapp = 4.77 × 103 M− 1), calculated using UV–Vis spectra indicating an adequate complex formation between CTDNA and PH. A dynamic mode of the fluorescence quenching mechanism in case of ethidium bromide (EB) + CTDNA by PH has been observed confirming formation of DNA-PH complex. A moderate binding constants of PH with CTDNA + EB has been observed (2.74 × 104 M− 1 at 293 K) by means of fluorescence data. Calculated values of thermodynamic parameters enthalpy change (ΔH) and entropy change (ΔS), suggests weak (van der Walls like) force and hydrogen bonds playing the main role in the binding of PH to CTDNA. Furthermore, the results of circular dichroism (CD) reveal that PH does not disturb native conformation of CTDNA. As observed from absorption and fluorescence spectroscopy the binding mode of PH with DNA was indicative of a non-intercalative binding, which was supposed to be a groove binding. The molecular modeling results show that PH is capable of binding DNA having docking binding energy = -7.26 kcal × mol− 1. Above mentioned experimental results are found to be in consonance with molecular docking simulations and supports the CTDNA-PH binding. © 2017, Springer Science+Business Media, LLC, part of Springer Nature.en_US
dc.language.isoenen_US
dc.publisherSpringer New York LLCen_US
dc.sourceJournal of Fluorescenceen_US
dc.subjectBinsen_US
dc.subjectComplexationen_US
dc.subjectDichroismen_US
dc.subjectDNAen_US
dc.subjectDockingen_US
dc.subjectFluorescenceen_US
dc.subjectFluorescence spectroscopyen_US
dc.subjectHydrogen bondsen_US
dc.subjectMolecular modelingen_US
dc.subjectpHen_US
dc.subjectPhosphorusen_US
dc.subjectQuenchingen_US
dc.subjectSpectroscopyen_US
dc.subjectAbsorption and fluorescence spectroscopyen_US
dc.subjectApparent association constantsen_US
dc.subjectCalf thymus DNA (ct-DNA)en_US
dc.subjectCTDNAen_US
dc.subjectFluorescence quenching mechanismen_US
dc.subjectInteractionen_US
dc.subjectMolecular docking simulationsen_US
dc.subjectThermodynamic parameteren_US
dc.subjectBinding energyen_US
dc.subjectcalf thymus DNAen_US
dc.subjectDNAen_US
dc.subjectorganophosphorus compounden_US
dc.subjectanimalen_US
dc.subjectbovineen_US
dc.subjectchemistryen_US
dc.subjectconformationen_US
dc.subjectmetabolismen_US
dc.subjectmolecular dockingen_US
dc.subjectmolecular modelen_US
dc.subjectproceduresen_US
dc.subjectspectrofluorometryen_US
dc.subjectAnimalsen_US
dc.subjectCattleen_US
dc.subjectDNAen_US
dc.subjectModels, Molecularen_US
dc.subjectMolecular Conformationen_US
dc.subjectMolecular Docking Simulationen_US
dc.subjectOrganophosphorus Compoundsen_US
dc.subjectSpectrometry, Fluorescenceen_US
dc.titleSpectroscopic Evidence of Phosphorous Heterocycle–DNA Interaction and its Verification by Docking Approachen_US
dc.typeJournal Articleen_US
Appears in Collections:Department of Physics

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

Altmetric Badge: