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DC Field | Value | Language |
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dc.contributor.author | Noothi, Sunil K | - |
dc.contributor.author | Kombrabail, Mamata | - |
dc.contributor.author | Kundu, Tapas K | - |
dc.contributor.author | Krishnamoorthy, G | - |
dc.contributor.author | Rao, Basuthkar J | - |
dc.date.accessioned | 2012-02-13T10:55:33Z | - |
dc.date.available | 2012-02-13T10:55:33Z | - |
dc.date.issued | 2009-01 | - |
dc.identifier | 1742-464X | en_US |
dc.identifier.citation | FEBS Journal 276(2), 541-551 (2009) | en_US |
dc.identifier.uri | https://libjncir.jncasr.ac.in/xmlui/10572/397 | - |
dc.description | Restricted Access | en_US |
dc.description.abstract | We report a study of dynamics with a dsDNA-specific dye called PicoGreen bound to plasmid DNA (3.4 kb), and show that at low dye/DNA phosphate ratios (1 : 100 and below), PicoGreen dynamics reflect the motional dynamics of dsDNA. We further evaluated the usefulness of this probe by measuring the time-resolved fluorescence dynamics of PicoGreen bound to dsDNA in the presence of cationic reagents that affect DNA dynamics [MgCl2 and polyethyleneimine (PEI)] and also with plasmid DNA in different topological states. Among these conditions, MgCl2, PEI and the supercoiled form of plasmid resulted in increases in the very short component (0.2-0.4 ns) of the rotational correlation time. Separately, HMGB1 protein enhanced DNA dynamics, as observed from the rotational correlation times of very short (0.2-0.4 ns) and short (2-4 ns) rotational correlation timescale components. By studying the effect of specific deletion mutants HMGB1-Delta A (deletion of 98 N-terminal amino acids) and HMGB1-Delta C (deletion of 30 C-terminal amino acids), we show that the acidic C-terminal tail is required for enhancement of DNA dynamics. We then discuss the possible mechanisms and implications of HMGB1-mediated flexibility of DNA in the context of formation of large nucleoprotein complexes. | en_US |
dc.description.sponsorship | Tata Institute of Fundamental Research. Kanwal Rekhi Career Development. | en_US |
dc.description.uri | http://dx.doi.org/10.1111/j.1742-4658.2008.06802.x | en_US |
dc.language.iso | en | en_US |
dc.publisher | Wiley-BLackwell Publishing | en_US |
dc.rights | © 2009 FEBS | en_US |
dc.subject | anisotropy decay kinetics | en_US |
dc.subject | chromatin remodelling | en_US |
dc.subject | DNA dynamics | en_US |
dc.subject | HMGB1 | en_US |
dc.subject | PicoGreen | en_US |
dc.subject | Double-Stranded Dna | en_US |
dc.subject | Metal-Ligand Complex | en_US |
dc.subject | Molecular-Dynamics | en_US |
dc.subject | Energy Migration | en_US |
dc.subject | Structural Basis | en_US |
dc.subject | Hmgb Proteins | en_US |
dc.subject | Hoechst 33258 | en_US |
dc.subject | Binding | en_US |
dc.subject | Fluorescence | en_US |
dc.subject | Transcription | en_US |
dc.title | Enhanced DNA dynamics due to cationic reagents, topological states of dsDNA and high mobility group box 1 as probed by PicoGreen | en_US |
dc.type | Article | en_US |
Appears in Collections: | Research Papers (Tapas K. Kundu) |
Files in This Item:
File | Description | Size | Format | |
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2009 FEBS Journal 276 541–551.pdf Restricted Access | 268.23 kB | Adobe PDF | View/Open Request a copy |
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