The Use of Ultraviolet Resonance Raman Spectroscopy in the Analysis of Ionizing-Radiation-Induced Damage in DNA
Ultraviolet resonance Raman spectroscopy (UVRRS) was used to determine damage done in both calf-thymus DNA (CT-DNA) and a short stranded DNA oligomer (SS-DNA) due to ionizing radiation from a medical 60Co radiation therapy unit used in the treatment of cancer. Spectra were acquired at incident UV wa...
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Veröffentlicht in: | Applied spectroscopy 2009-04, Vol.63 (4), p.412-422 |
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description | Ultraviolet resonance Raman spectroscopy (UVRRS) was used to determine damage done in both calf-thymus DNA (CT-DNA) and a short stranded DNA oligomer (SS-DNA) due to ionizing radiation from a medical 60Co radiation therapy unit used in the treatment of cancer. Spectra were acquired at incident UV wavelengths of 248, 257, and 264 nm in order to utilize the differences in UVRR cross-sections of the bases with wavelength. Through the analysis of difference spectra between irradiated and unirradiated DNA at each of the incident UV wavelengths, damage to CT- and SS-DNA was observed and identified. Significant radiation-induced increases in the difference spectra of the CT-DNA indicated disruption of the stable, stacked structure of its bases, as well as the disruption of Watson–Crick hydrogen bonds between the base pairs. Base unstacking was not as evident in the SS-DNA, while radiation-induced spectral decreases suggest disruption of the structure of the nucleotides. As demonstrated, UVRRS has the ability to highlight contributions from specific moieties with the use of varying incident UV wavelengths, thus enhancing the already information-rich content of the Raman spectra. |
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P. ; Jirasek, A.</creator><creatorcontrib>Shaw, C. P. ; Jirasek, A.</creatorcontrib><description>Ultraviolet resonance Raman spectroscopy (UVRRS) was used to determine damage done in both calf-thymus DNA (CT-DNA) and a short stranded DNA oligomer (SS-DNA) due to ionizing radiation from a medical 60Co radiation therapy unit used in the treatment of cancer. Spectra were acquired at incident UV wavelengths of 248, 257, and 264 nm in order to utilize the differences in UVRR cross-sections of the bases with wavelength. Through the analysis of difference spectra between irradiated and unirradiated DNA at each of the incident UV wavelengths, damage to CT- and SS-DNA was observed and identified. Significant radiation-induced increases in the difference spectra of the CT-DNA indicated disruption of the stable, stacked structure of its bases, as well as the disruption of Watson–Crick hydrogen bonds between the base pairs. Base unstacking was not as evident in the SS-DNA, while radiation-induced spectral decreases suggest disruption of the structure of the nucleotides. As demonstrated, UVRRS has the ability to highlight contributions from specific moieties with the use of varying incident UV wavelengths, thus enhancing the already information-rich content of the Raman spectra.</description><identifier>ISSN: 0003-7028</identifier><identifier>EISSN: 1943-3530</identifier><identifier>DOI: 10.1366/000370209787944325</identifier><identifier>PMID: 19366507</identifier><language>eng</language><publisher>London, England: SAGE Publications</publisher><subject>Animals ; Base Pairing ; Cattle ; DNA - chemistry ; DNA - radiation effects ; DNA Damage - radiation effects ; Hydrogen Bonding ; Nucleotides - chemistry ; Nucleotides - radiation effects ; Radiation, Ionizing ; Spectrophotometry, Ultraviolet ; Spectrum Analysis, Raman - instrumentation ; Spectrum Analysis, Raman - methods ; Thymus Gland - chemistry ; Thymus Gland - radiation effects</subject><ispartof>Applied spectroscopy, 2009-04, Vol.63 (4), p.412-422</ispartof><rights>2009 Society for Applied Spectroscopy</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c439t-3df0c23e178df398774a85c179f3bffd1fb8b3d0f21e26b9565724938a753ba33</citedby><cites>FETCH-LOGICAL-c439t-3df0c23e178df398774a85c179f3bffd1fb8b3d0f21e26b9565724938a753ba33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1366/000370209787944325$$EPDF$$P50$$Gsage$$H</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.1366/000370209787944325$$EHTML$$P50$$Gsage$$H</linktohtml><link.rule.ids>314,780,784,21819,27924,27925,43621,43622</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19366507$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shaw, C. P.</creatorcontrib><creatorcontrib>Jirasek, A.</creatorcontrib><title>The Use of Ultraviolet Resonance Raman Spectroscopy in the Analysis of Ionizing-Radiation-Induced Damage in DNA</title><title>Applied spectroscopy</title><addtitle>Appl Spectrosc</addtitle><description>Ultraviolet resonance Raman spectroscopy (UVRRS) was used to determine damage done in both calf-thymus DNA (CT-DNA) and a short stranded DNA oligomer (SS-DNA) due to ionizing radiation from a medical 60Co radiation therapy unit used in the treatment of cancer. Spectra were acquired at incident UV wavelengths of 248, 257, and 264 nm in order to utilize the differences in UVRR cross-sections of the bases with wavelength. Through the analysis of difference spectra between irradiated and unirradiated DNA at each of the incident UV wavelengths, damage to CT- and SS-DNA was observed and identified. Significant radiation-induced increases in the difference spectra of the CT-DNA indicated disruption of the stable, stacked structure of its bases, as well as the disruption of Watson–Crick hydrogen bonds between the base pairs. Base unstacking was not as evident in the SS-DNA, while radiation-induced spectral decreases suggest disruption of the structure of the nucleotides. As demonstrated, UVRRS has the ability to highlight contributions from specific moieties with the use of varying incident UV wavelengths, thus enhancing the already information-rich content of the Raman spectra.</description><subject>Animals</subject><subject>Base Pairing</subject><subject>Cattle</subject><subject>DNA - chemistry</subject><subject>DNA - radiation effects</subject><subject>DNA Damage - radiation effects</subject><subject>Hydrogen Bonding</subject><subject>Nucleotides - chemistry</subject><subject>Nucleotides - radiation effects</subject><subject>Radiation, Ionizing</subject><subject>Spectrophotometry, Ultraviolet</subject><subject>Spectrum Analysis, Raman - instrumentation</subject><subject>Spectrum Analysis, Raman - methods</subject><subject>Thymus Gland - chemistry</subject><subject>Thymus Gland - radiation effects</subject><issn>0003-7028</issn><issn>1943-3530</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kc9LwzAYhoMoOqf_gAfJSU91Sb-maY5j_hqIwnTnkqaJRrpkNq0w_3pTNvAg7PTxwfO8h_dF6IKSGwp5PiGEACcpEbzgIssgZQdoREUGCTAgh2g0AEkkihN0GsJnfJkAdoxOqIg-I3yE_NuHxsugsTd42XSt_La-0R1e6OCddErjhVxJh1_XWnWtD8qvN9g63EVt6mSzCTYM7tw7-2Pde7KQtZWd9S6Zu7pXusa3MeBdD9Lt8_QMHRnZBH2-u2O0vL97mz0mTy8P89n0KVEZiC6B2hCVgqa8qA2IgvNMFkxRLgxUxtTUVEUFNTEp1WleCZYznmYCCskZVBJgjK63uevWf_U6dOXKBqWbRjrt-1DyLMtzUeQDebWXzDlNBecDmG5BFXsIrTblurUr2W5KSsphkPL_IFG63KX31UrXf8pugQhMtkCIJZWfvm9jq2Ff5C-yxJKZ</recordid><startdate>200904</startdate><enddate>200904</enddate><creator>Shaw, C. P.</creator><creator>Jirasek, A.</creator><general>SAGE Publications</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7TM</scope></search><sort><creationdate>200904</creationdate><title>The Use of Ultraviolet Resonance Raman Spectroscopy in the Analysis of Ionizing-Radiation-Induced Damage in DNA</title><author>Shaw, C. P. ; Jirasek, A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c439t-3df0c23e178df398774a85c179f3bffd1fb8b3d0f21e26b9565724938a753ba33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Animals</topic><topic>Base Pairing</topic><topic>Cattle</topic><topic>DNA - chemistry</topic><topic>DNA - radiation effects</topic><topic>DNA Damage - radiation effects</topic><topic>Hydrogen Bonding</topic><topic>Nucleotides - chemistry</topic><topic>Nucleotides - radiation effects</topic><topic>Radiation, Ionizing</topic><topic>Spectrophotometry, Ultraviolet</topic><topic>Spectrum Analysis, Raman - instrumentation</topic><topic>Spectrum Analysis, Raman - methods</topic><topic>Thymus Gland - chemistry</topic><topic>Thymus Gland - radiation effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shaw, C. P.</creatorcontrib><creatorcontrib>Jirasek, A.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Nucleic Acids Abstracts</collection><jtitle>Applied spectroscopy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shaw, C. P.</au><au>Jirasek, A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Use of Ultraviolet Resonance Raman Spectroscopy in the Analysis of Ionizing-Radiation-Induced Damage in DNA</atitle><jtitle>Applied spectroscopy</jtitle><addtitle>Appl Spectrosc</addtitle><date>2009-04</date><risdate>2009</risdate><volume>63</volume><issue>4</issue><spage>412</spage><epage>422</epage><pages>412-422</pages><issn>0003-7028</issn><eissn>1943-3530</eissn><abstract>Ultraviolet resonance Raman spectroscopy (UVRRS) was used to determine damage done in both calf-thymus DNA (CT-DNA) and a short stranded DNA oligomer (SS-DNA) due to ionizing radiation from a medical 60Co radiation therapy unit used in the treatment of cancer. Spectra were acquired at incident UV wavelengths of 248, 257, and 264 nm in order to utilize the differences in UVRR cross-sections of the bases with wavelength. Through the analysis of difference spectra between irradiated and unirradiated DNA at each of the incident UV wavelengths, damage to CT- and SS-DNA was observed and identified. Significant radiation-induced increases in the difference spectra of the CT-DNA indicated disruption of the stable, stacked structure of its bases, as well as the disruption of Watson–Crick hydrogen bonds between the base pairs. Base unstacking was not as evident in the SS-DNA, while radiation-induced spectral decreases suggest disruption of the structure of the nucleotides. As demonstrated, UVRRS has the ability to highlight contributions from specific moieties with the use of varying incident UV wavelengths, thus enhancing the already information-rich content of the Raman spectra.</abstract><cop>London, England</cop><pub>SAGE Publications</pub><pmid>19366507</pmid><doi>10.1366/000370209787944325</doi><tpages>11</tpages></addata></record> |
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subjects | Animals Base Pairing Cattle DNA - chemistry DNA - radiation effects DNA Damage - radiation effects Hydrogen Bonding Nucleotides - chemistry Nucleotides - radiation effects Radiation, Ionizing Spectrophotometry, Ultraviolet Spectrum Analysis, Raman - instrumentation Spectrum Analysis, Raman - methods Thymus Gland - chemistry Thymus Gland - radiation effects |
title | The Use of Ultraviolet Resonance Raman Spectroscopy in the Analysis of Ionizing-Radiation-Induced Damage in DNA |
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