Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1488
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dc.contributor.authorGANESH, KRISHNA N.en_US
dc.contributor.authorSharma, Nagendra K.en_US
dc.date.accessioned2019-01-21T10:29:25Z
dc.date.available2019-01-21T10:29:25Z
dc.date.issued2011-02en_US
dc.identifier.citationOrganic and Biomolecular Chemistry, (9).en_US
dc.identifier.issn1477-0520en_US
dc.identifier.issn1477-0539en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1488-
dc.identifier.urihttps://doi.org/10.1039/C0OB00528Ben_US
dc.description.abstractNucleic (DNA) acids having contiguous stretch of G sequence form quadruplex structure, which is very critical to control cell division. Recently the existence of G-quadruplex in RNA is also reported in presence of monovalent metal ion. PNA is a promising DNA analogue which binds strongly to DNA to form PNA-:-DNA duplex or PNA2-:-DNA triplex. PNA also forms quadruplexes such G-quadruplex and i-motif in G and C-rich sequences respectively. aep-PNA containing a prolyl ring is one of several PNA analogues that provide rigidity and chirality in backbone and has binding affinity to natural DNA which is higher than that of PNA. Here we examine the ability of aep-PNA-G to form a quadruplex by UV, CD and mass spectroscopic techniques.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectNucleic (DNA)en_US
dc.subjectPNA analoguesen_US
dc.subjectG-quadruplexen_US
dc.subjectMonovalent metalen_US
dc.subject2011en_US
dc.titleEnhanced stability of G-quadruplexes from conformationally constrained aep-PNA backboneen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleOrganic and Biomolecular Chemistryen_US
dc.publication.originofpublisherForeignen_US
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