Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/3923
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dc.contributor.authorMajee, Prativaen_US
dc.contributor.authorKumar Mishra, Subodhen_US
dc.contributor.authorPandya, Niralien_US
dc.contributor.authorShankar, Umaen_US
dc.contributor.authorNayak, Debasisen_US
dc.contributor.authorKumar, Amiten_US
dc.date.accessioned2022-03-17T01:00:00Z-
dc.date.accessioned2022-03-17T15:31:02Z-
dc.date.available2022-03-17T01:00:00Z-
dc.date.available2022-03-17T15:31:02Z-
dc.date.issued2020-
dc.identifier.citationMajee, P., Kumar Mishra, S., Pandya, N., Shankar, U., Pasadi, S., Muniyappa, K., . . . Kumar, A. (2020). Identification and characterization of two conserved G-quadruplex forming motifs in the nipah virus genome and their interaction with G-quadruplex specific ligands. Scientific Reports, 10(1) doi:10.1038/s41598-020-58406-8en_US
dc.identifier.issn2045-2322-
dc.identifier.otherEID(2-s2.0-85078710377)-
dc.identifier.urihttps://doi.org/10.1038/s41598-020-58406-8-
dc.identifier.urihttps://dspace.iiti.ac.in/handle/123456789/3923-
dc.description.abstractThe G-quadruplex (GQ) motifs are considered as potential drug-target sites for several human pathogenic viruses such as Zika, Hepatitis, Ebola, and Human Herpesviruses. The recent outbreaks of Nipah virus (NiV) in India, the highly fatal emerging zoonotic virus is a potential threat to global health security as no anti-viral drug or vaccine in currently available. Therefore, here in the present study, we sought to assess the ability of the putative G-quadruplex forming sequences in the NiV genome to form G-quadruplex structures and act as targets for anti-viral compounds. Bioinformatics analysis underpinned by various biophysical and biochemical techniques (such as NMR, CD, EMSA, DMS footprinting assay) confirmed the presence of two highly conserved G-quadruplex forming sequences (HGQs) in the G and L genes of NiV. These genes encode the cell attachment glycoprotein and RNA-dependent RNA polymerase, respectively and are essential for the virus entry and replication within the host cell. It remains possible that stabilization of these HGQs by the known G-quadruplex binding ligands like TMPyP4 and Braco-19 represents a promising strategy to inhibit the expression of the HGQ harboring genes and thereby stop the viral entry and replication inside the host cell. Accordingly, we report for the first time, that HGQs in Nipah virus genome are targets for G-quadruplex specific ligands; therefore, could serve as potential targets for anti-viral therapy. © 2020, The Author(s).en_US
dc.language.isoenen_US
dc.publisherNature Researchen_US
dc.sourceScientific Reportsen_US
dc.subjectacridine derivativeen_US
dc.subjectantivirus agenten_US
dc.subjectBRACO-19en_US
dc.subjectguanine quadruplexen_US
dc.subjectliganden_US
dc.subjectporphyrinen_US
dc.subjecttetra(4-N-methylpyridyl)porphineen_US
dc.subjectbiologyen_US
dc.subjectconserved sequenceen_US
dc.subjectdrug effecten_US
dc.subjectgeneticsen_US
dc.subjectHenipavirus infectionen_US
dc.subjecthumanen_US
dc.subjecthydrogen bonden_US
dc.subjectIndiaen_US
dc.subjectNipah virusen_US
dc.subjectphysiologyen_US
dc.subjectvirologyen_US
dc.subjectvirus entryen_US
dc.subjectvirus genomeen_US
dc.subjectvirus replicationen_US
dc.subjectAcridinesen_US
dc.subjectAntiviral Agentsen_US
dc.subjectComputational Biologyen_US
dc.subjectConserved Sequenceen_US
dc.subjectG-Quadruplexesen_US
dc.subjectGenome, Viralen_US
dc.subjectHenipavirus Infectionsen_US
dc.subjectHumansen_US
dc.subjectHydrogen Bondingen_US
dc.subjectIndiaen_US
dc.subjectLigandsen_US
dc.subjectNipah Virusen_US
dc.subjectPorphyrinsen_US
dc.subjectVirus Internalizationen_US
dc.subjectVirus Replicationen_US
dc.titleIdentification and characterization of two conserved G-quadruplex forming motifs in the Nipah virus genome and their interaction with G-quadruplex specific ligandsen_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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