Confocal fluorescence imaging of photosensitized DNA denaturation in cell nuclei.

The double-stranded helical structure of DNA is maintained in part by hydrogen bonds between strands and by stacking interactions between adjacent purine and pyrimidine bases in one strand. The transition (denaturation) from a double-stranded (ds) to a single-stranded (ss) form can be induced in iso...

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Main Authors: Bernas, T, Asem, E, Robinson, J, Cook, P, Dobrucki, J
Format: Journal article
Language:English
Published: 2005
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author Bernas, T
Asem, E
Robinson, J
Cook, P
Dobrucki, J
author_facet Bernas, T
Asem, E
Robinson, J
Cook, P
Dobrucki, J
author_sort Bernas, T
collection OXFORD
description The double-stranded helical structure of DNA is maintained in part by hydrogen bonds between strands and by stacking interactions between adjacent purine and pyrimidine bases in one strand. The transition (denaturation) from a double-stranded (ds) to a single-stranded (ss) form can be induced in isolated DNA or fixed cells by exposure to elevated temperatures, alkali or acids, aprotic or nonpolar solvents or some drugs. We report here that DNA denaturation can occur in situ in cell nuclei as a result of interaction between light and an intercalated dye, acridine orange or ethidium bromide. This DNA photodenaturation was probed using metachromatic properties of acridine orange and imaged by fluorescence confocal microscopy. Furthermore, an empirical kinetic model was developed to separate changes of acridine orange luminescence intensities caused by photobleaching from those that were a result of DNA denaturation. We investigated the influence of oxygen on these phenomena and propose a mechanism by which photodenaturation may occur.
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spelling oxford-uuid:6d12a821-bab8-44aa-9bce-6bdcfce374fe2022-03-26T19:15:28ZConfocal fluorescence imaging of photosensitized DNA denaturation in cell nuclei.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:6d12a821-bab8-44aa-9bce-6bdcfce374feEnglishSymplectic Elements at Oxford2005Bernas, TAsem, ERobinson, JCook, PDobrucki, JThe double-stranded helical structure of DNA is maintained in part by hydrogen bonds between strands and by stacking interactions between adjacent purine and pyrimidine bases in one strand. The transition (denaturation) from a double-stranded (ds) to a single-stranded (ss) form can be induced in isolated DNA or fixed cells by exposure to elevated temperatures, alkali or acids, aprotic or nonpolar solvents or some drugs. We report here that DNA denaturation can occur in situ in cell nuclei as a result of interaction between light and an intercalated dye, acridine orange or ethidium bromide. This DNA photodenaturation was probed using metachromatic properties of acridine orange and imaged by fluorescence confocal microscopy. Furthermore, an empirical kinetic model was developed to separate changes of acridine orange luminescence intensities caused by photobleaching from those that were a result of DNA denaturation. We investigated the influence of oxygen on these phenomena and propose a mechanism by which photodenaturation may occur.
spellingShingle Bernas, T
Asem, E
Robinson, J
Cook, P
Dobrucki, J
Confocal fluorescence imaging of photosensitized DNA denaturation in cell nuclei.
title Confocal fluorescence imaging of photosensitized DNA denaturation in cell nuclei.
title_full Confocal fluorescence imaging of photosensitized DNA denaturation in cell nuclei.
title_fullStr Confocal fluorescence imaging of photosensitized DNA denaturation in cell nuclei.
title_full_unstemmed Confocal fluorescence imaging of photosensitized DNA denaturation in cell nuclei.
title_short Confocal fluorescence imaging of photosensitized DNA denaturation in cell nuclei.
title_sort confocal fluorescence imaging of photosensitized dna denaturation in cell nuclei
work_keys_str_mv AT bernast confocalfluorescenceimagingofphotosensitizeddnadenaturationincellnuclei
AT aseme confocalfluorescenceimagingofphotosensitizeddnadenaturationincellnuclei
AT robinsonj confocalfluorescenceimagingofphotosensitizeddnadenaturationincellnuclei
AT cookp confocalfluorescenceimagingofphotosensitizeddnadenaturationincellnuclei
AT dobruckij confocalfluorescenceimagingofphotosensitizeddnadenaturationincellnuclei