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dc.contributor.authorNeethu, S-
dc.contributor.authorSuresh, C H-
dc.contributor.authorThresia, T-
dc.contributor.authorThomas, T J-
dc.contributor.authorPillai, C K S-
dc.date.accessioned2015-08-27T07:34:01Z-
dc.date.available2015-08-27T07:34:01Z-
dc.date.issued2008-
dc.identifier.citationBiomacromolecules 9(7):1860-1869;Jul 2008en_US
dc.identifier.issn1525-7797-
dc.identifier.urihttp://ir.niist.res.in:8080/jspui/handle/123456789/1985-
dc.description.abstractThe ability of Li+, Na+, K+, Rb+, CS+, Mg2+, Ca2+, Sr2+, Ba2+, Cu2+, Cd2+, Al3+, V4+, Hg2+, Pd2+, Au3+, and Pt4+ to provoke liquid crystalline (LC) phases in high molecular weight DNA was investigated. The alkali and alkaline earth metal ions provoked typical cholesteric/columnar structures, whereas transition metal ions precipitated DNA into solid/translucent gel-like aggregates. Heavy metal ions reduced viscosity of DNA solution, disrupting rigid, rod-like DNA structure necessary for LC textures. Three-layer quantum mechanical-molecular mechanical (QM/MM) studies of Li+, Na+, K+, Mg2+, and Ca2+ binding DNA fragment suggested several possible binding modes of these ions to the phosphate groups. The dianion mode of metal binding, involving the phosphate groups of both strands of DNA, allowed for higher DNA binding affinity of the alkaline earth metal ions. These results have implications in understanding the biological role of metal ions and developing DNA-based sensors and nanoelectronic devices.en_US
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.subjectCondensed DNAen_US
dc.subjectNucleic-acidsen_US
dc.subjectRaman-spectroscopyen_US
dc.subjectDivalent-cationsen_US
dc.subjectSynthetic polyaminesen_US
dc.subjectStranded DNAen_US
dc.subjectCalf-thymus DNAen_US
dc.titleLiquid crystalline phase behavior of high molecular weight DNA: A comparative study of the influence of metal ions of different size, charge and binding modeen_US
dc.typeArticleen_US
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