Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/3931
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dc.contributor.authorShankar, Umaen_US
dc.contributor.authorJain, Nehaen_US
dc.contributor.authorMajee, Prativaen_US
dc.contributor.authorKodgire, Prashanten_US
dc.contributor.authorKumar, Amiten_US
dc.date.accessioned2022-03-17T01:00:00Z-
dc.date.accessioned2022-03-17T15:31:04Z-
dc.date.available2022-03-17T01:00:00Z-
dc.date.available2022-03-17T15:31:04Z-
dc.date.issued2020-
dc.identifier.citationShankar, U., Jain, N., Majee, P., Kodgire, P., Sharma, T. K., & Kumar, A. (2020). Exploring computational and biophysical tools to study the presence of G-quadruplex structures: A promising therapeutic solution for drug-resistant vibrio cholerae. Frontiers in Genetics, 11 doi:10.3389/fgene.2020.00935en_US
dc.identifier.issn1664-8021-
dc.identifier.otherEID(2-s2.0-85092369344)-
dc.identifier.urihttps://doi.org/10.3389/fgene.2020.00935-
dc.identifier.urihttps://dspace.iiti.ac.in/handle/123456789/3931-
dc.description.abstractVibrio cholerae, a gram-negative bacterium that causes cholera, has already caused seven major pandemics across the world and infects roughly 1.3–4 million people every year. Cholera treatment primarily involves oral rehydration therapy supplemented with antibiotics. But recently, multidrug-resistant strains of V. cholerae have emerged. High genomic plasticity further enhances the pathogenesis of this human pathogen. Guanines in DNA or RNA assemble to form G-quadruplex (GQ) structures which have begun to be seen as potential drug targeting sites for different pathogenic bacteria and viruses. In this perspective, we carried out a genome-wide hunt in V. cholerae using a bio-informatics approach and observed ∼85 G-quadruplex forming motifs (VC-PGQs) in chromosome I and ∼45 putative G-quadruplexs (PGQs) in chromosome II. Ten putative G-quadruplex forming motifs (VC-PGQs) were selected on the basis of conservation throughout the genus and functional analysis displayed their location in the essential genes encoding bacterial proteins, for example, methyl-accepting chemotaxis protein, orotate phosphoribosyl transferase protein, amidase proteins, etc. The predicted VC-PGQs were validated using different bio-physical techniques, including Nuclear Magnetic Resonance spectroscopy, Circular Dichroism spectroscopy, and electrophoretic mobility shift assay, which demonstrated the formation of highly stable GQ structures in the bacteria. The interaction of these VC-PGQs with the known specific GQ ligand, TMPyP4, was analyzed using ITC and molecular dynamics studies that displayed the stabilization of the VC-PGQs by the GQ ligands and thus represents a potential therapeutic strategy against this enteric pathogen by inhibiting the PGQ harboring gene expression, thereby inhibiting the bacterial growth and virulence. In summary, this study reveals the presence of conserved GQ forming motifs in the V. cholerae genome that has the potential to be used to treat the multi-drug resistance problem of the notorious enteric pathogen. © Copyright © 2020 Shankar, Jain, Majee, Kodgire, Sharma and Kumar.en_US
dc.language.isoenen_US
dc.publisherFrontiers Media S.A.en_US
dc.sourceFrontiers in Geneticsen_US
dc.subjectamidaseen_US
dc.subjectamoxicillinen_US
dc.subjectantibiotic agenten_US
dc.subjectbacterial proteinen_US
dc.subjectoligonucleotideen_US
dc.subjectphosphoribosyltransferaseen_US
dc.subjectArticleen_US
dc.subjectbacterial genomeen_US
dc.subjectbinding affinityen_US
dc.subjectbinding siteen_US
dc.subjectbiophysicsen_US
dc.subjectchemotaxisen_US
dc.subjectcircular dichroismen_US
dc.subjectconformational transitionen_US
dc.subjectDNA bindingen_US
dc.subjectdrug targetingen_US
dc.subjectenthalpyen_US
dc.subjectenzyme active siteen_US
dc.subjectgel mobility shift assayen_US
dc.subjectgene frequencyen_US
dc.subjectIC50en_US
dc.subjectinfrared spectroscopyen_US
dc.subjectinhibition constanten_US
dc.subjectisothermal titration calorimetryen_US
dc.subjectmolecular dockingen_US
dc.subjectmolecular dynamicsen_US
dc.subjectmultidrug resistanceen_US
dc.subjectnonhumanen_US
dc.subjectnucleotide sequenceen_US
dc.subjectoral rehydration therapyen_US
dc.subjectpromoter regionen_US
dc.subjectprotein conformationen_US
dc.subjectprotein secondary structureen_US
dc.subjectproton nuclear magnetic resonanceen_US
dc.subjecttelomere lengthen_US
dc.subjectVibrio choleraeen_US
dc.titleExploring Computational and Biophysical Tools to Study the Presence of G-Quadruplex Structures: A Promising Therapeutic Solution for Drug-Resistant Vibrio choleraeen_US
dc.typeJournal Articleen_US
dc.rights.licenseAll Open Access, Gold, Green-
Appears in Collections:Department of Biosciences and Biomedical Engineering

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