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(Bi)sulfite Oxidation by Copper,Zinc-Superoxide Dismutase: Sulfite-Derived, Radical-Initiated Protein Radical Formation
Background: Sulfur dioxide, formed during the combustion of fossil fuels, is a major air pollutant near large cities. Its two ionized forms in aqueous solution, sulfite and (bi)sulfite, are widely used as preservatives and antioxidants to prevent food and beverage spoilage. (Bi)sulfite can be oxidiz...
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Published in: | Environmental health perspectives 2010-07, Vol.118 (7), p.970-975 |
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description | Background: Sulfur dioxide, formed during the combustion of fossil fuels, is a major air pollutant near large cities. Its two ionized forms in aqueous solution, sulfite and (bi)sulfite, are widely used as preservatives and antioxidants to prevent food and beverage spoilage. (Bi)sulfite can be oxidized by peroxidases to form the very reactive sulfur trioxide anion radical (•SO3−). This free radical further reacts with oxygen to form the peroxymonosulfate anion radical (−O3SOO•) and sulfate anion radical (SO4•−). Objective: To explore the critical role of these radical intermediates in further oxidizing biomolecules, we examined the ability of copper,zinc-superoxide dismutase (Cu,Zn-SOD) to initiate this radical chain reaction, using human serum albumin (HSA) as a model target. Methods: We used electron paramagnetic resonance, optical spectroscopy, oxygen uptake, and immuno-spin trapping to study the protein oxidations driven by sulfite-derived radicals. Results: We found that when Cu,Zn-SOD reacted with (bi)sulfite, •SO3− was produced, with the concomitant reduction of SOD-Cu(II) to SOD-Cu(I). Further, we demonstrated that sulfite oxidation mediated by Cu,Zn-SOD induced the formation of radical-derived 5,5-dimethyl-1-pyrroline N-oxide (DMPO) spin-trapped HSA radicals. Conclusions: The present study suggests that protein oxidative damage resulting from (bi)sulfite oxidation promoted by Cu,Zn-SOD could be involved in oxidative damage and tissue injury in (bi)sulfite-exacerbated allergic reactions. |
doi_str_mv | 10.1289/ehp.0901533 |
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Its two ionized forms in aqueous solution, sulfite and (bi)sulfite, are widely used as preservatives and antioxidants to prevent food and beverage spoilage. (Bi)sulfite can be oxidized by peroxidases to form the very reactive sulfur trioxide anion radical (•SO3−). This free radical further reacts with oxygen to form the peroxymonosulfate anion radical (−O3SOO•) and sulfate anion radical (SO4•−). Objective: To explore the critical role of these radical intermediates in further oxidizing biomolecules, we examined the ability of copper,zinc-superoxide dismutase (Cu,Zn-SOD) to initiate this radical chain reaction, using human serum albumin (HSA) as a model target. Methods: We used electron paramagnetic resonance, optical spectroscopy, oxygen uptake, and immuno-spin trapping to study the protein oxidations driven by sulfite-derived radicals. Results: We found that when Cu,Zn-SOD reacted with (bi)sulfite, •SO3− was produced, with the concomitant reduction of SOD-Cu(II) to SOD-Cu(I). Further, we demonstrated that sulfite oxidation mediated by Cu,Zn-SOD induced the formation of radical-derived 5,5-dimethyl-1-pyrroline N-oxide (DMPO) spin-trapped HSA radicals. Conclusions: The present study suggests that protein oxidative damage resulting from (bi)sulfite oxidation promoted by Cu,Zn-SOD could be involved in oxidative damage and tissue injury in (bi)sulfite-exacerbated allergic reactions.</description><identifier>ISSN: 0091-6765</identifier><identifier>EISSN: 1552-9924</identifier><identifier>DOI: 10.1289/ehp.0901533</identifier><identifier>PMID: 20348042</identifier><identifier>CODEN: EVHPAZ</identifier><language>eng</language><publisher>Research Triangle Park, NC: National Institute of Environmental Health Sciences</publisher><subject>Adducts ; Air Pollutants - metabolism ; Anions ; Biological and medical sciences ; Blotting, Western ; Chemical and industrial products toxicology. Toxic occupational diseases ; Chemical properties ; Copper in the body ; Cyclic N-Oxides - metabolism ; Electron paramagnetic resonance ; Electron Spin Resonance Spectroscopy ; Environment. Living conditions ; Enzyme-Linked Immunosorbent Assay ; Free radicals ; Free radicals (Chemistry) ; Health aspects ; Health savings accounts ; Humans ; Medical sciences ; Metals and various inorganic compounds ; Observations ; Oxidases ; Oxidation ; Oxidation-Reduction ; Oxidation-reduction reaction ; Oxidative Stress - physiology ; Oxygen ; Peroxides - metabolism ; Properties ; Public health. Hygiene ; Public health. Hygiene-occupational medicine ; Rosaniline Dyes ; Serum Albumin - metabolism ; Spectrum Analysis ; Spin Trapping ; Sulfites ; Sulfites - metabolism ; Superoxide Dismutase - metabolism ; Superoxides ; Toxicology ; Zinc compounds</subject><ispartof>Environmental health perspectives, 2010-07, Vol.118 (7), p.970-975</ispartof><rights>2015 INIST-CNRS</rights><rights>COPYRIGHT 2010 National Institute of Environmental Health Sciences</rights><rights>Copyright National Institute of Environmental Health Sciences Jul 2010</rights><rights>2010</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c585t-d85fed0b2bfbc1c2f7e290267abc27a3ef5a7270618c4f5045315e91192151533</citedby><cites>FETCH-LOGICAL-c585t-d85fed0b2bfbc1c2f7e290267abc27a3ef5a7270618c4f5045315e91192151533</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/27822953$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/27822953$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768,58213,58446</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=22997653$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20348042$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ranguelova, Kalina</creatorcontrib><creatorcontrib>Bonini, Marcelo G.</creatorcontrib><creatorcontrib>Mason, Ronald P.</creatorcontrib><title>(Bi)sulfite Oxidation by Copper,Zinc-Superoxide Dismutase: Sulfite-Derived, Radical-Initiated Protein Radical Formation</title><title>Environmental health perspectives</title><addtitle>Environ Health Perspect</addtitle><description>Background: Sulfur dioxide, formed during the combustion of fossil fuels, is a major air pollutant near large cities. Its two ionized forms in aqueous solution, sulfite and (bi)sulfite, are widely used as preservatives and antioxidants to prevent food and beverage spoilage. (Bi)sulfite can be oxidized by peroxidases to form the very reactive sulfur trioxide anion radical (•SO3−). This free radical further reacts with oxygen to form the peroxymonosulfate anion radical (−O3SOO•) and sulfate anion radical (SO4•−). Objective: To explore the critical role of these radical intermediates in further oxidizing biomolecules, we examined the ability of copper,zinc-superoxide dismutase (Cu,Zn-SOD) to initiate this radical chain reaction, using human serum albumin (HSA) as a model target. Methods: We used electron paramagnetic resonance, optical spectroscopy, oxygen uptake, and immuno-spin trapping to study the protein oxidations driven by sulfite-derived radicals. Results: We found that when Cu,Zn-SOD reacted with (bi)sulfite, •SO3− was produced, with the concomitant reduction of SOD-Cu(II) to SOD-Cu(I). Further, we demonstrated that sulfite oxidation mediated by Cu,Zn-SOD induced the formation of radical-derived 5,5-dimethyl-1-pyrroline N-oxide (DMPO) spin-trapped HSA radicals. Conclusions: The present study suggests that protein oxidative damage resulting from (bi)sulfite oxidation promoted by Cu,Zn-SOD could be involved in oxidative damage and tissue injury in (bi)sulfite-exacerbated allergic reactions.</description><subject>Adducts</subject><subject>Air Pollutants - metabolism</subject><subject>Anions</subject><subject>Biological and medical sciences</subject><subject>Blotting, Western</subject><subject>Chemical and industrial products toxicology. Toxic occupational diseases</subject><subject>Chemical properties</subject><subject>Copper in the body</subject><subject>Cyclic N-Oxides - metabolism</subject><subject>Electron paramagnetic resonance</subject><subject>Electron Spin Resonance Spectroscopy</subject><subject>Environment. Living conditions</subject><subject>Enzyme-Linked Immunosorbent Assay</subject><subject>Free radicals</subject><subject>Free radicals (Chemistry)</subject><subject>Health aspects</subject><subject>Health savings accounts</subject><subject>Humans</subject><subject>Medical sciences</subject><subject>Metals and various inorganic compounds</subject><subject>Observations</subject><subject>Oxidases</subject><subject>Oxidation</subject><subject>Oxidation-Reduction</subject><subject>Oxidation-reduction reaction</subject><subject>Oxidative Stress - physiology</subject><subject>Oxygen</subject><subject>Peroxides - metabolism</subject><subject>Properties</subject><subject>Public health. Hygiene</subject><subject>Public health. Hygiene-occupational medicine</subject><subject>Rosaniline Dyes</subject><subject>Serum Albumin - metabolism</subject><subject>Spectrum Analysis</subject><subject>Spin Trapping</subject><subject>Sulfites</subject><subject>Sulfites - metabolism</subject><subject>Superoxide Dismutase - metabolism</subject><subject>Superoxides</subject><subject>Toxicology</subject><subject>Zinc compounds</subject><issn>0091-6765</issn><issn>1552-9924</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><recordid>eNpdktFv1SAUxonRuOvVJ581zYxR4zqBlgI-mMw7p0uWzDh98YVQerpx05YKdLr_Xq6929TwAMn34zuc84HQY4L3CRXyDVyM-1hiworiDloQxmguJS3vogXGkuQVr9gOehDCGmNMRFXdRzsUF6XAJV2gny_f21dh6lobITv9ZRsdrRuy-ipbuXEEv_fdDiY_m9LRJRWyQxv6KeoAb7Oz-Vp-CN5eQrOXfdGNNbrLjwcbrY7QZJ-9i2CHayU7cr7_U-EhutfqLsCj7b5E344-fF19yk9OPx6vDk5ywwSLeSNYCw2uad3WhhjacqAS04rr2lCuC2iZ5pTjighTtgyXrCAMJCGSEraZyBK9m33Hqe6hMTBErzs1ettrf6WctupfZbAX6txdKippmh5PBi-2Bt79mCBE1dtgoOv0AG4KSnDOZFGmtUS7_5FrN_khdad4UXKBWSES9GyGznUHyg6tS1XNxlId0IIWosQVS9TrmTLeheChvXkwwWoTukqhq23oiX76d4837HXKCXi-BXRIKbReD8aGW45KmT7JxujJzK1DdP5W5yIhSf8NjjK-FQ</recordid><startdate>20100701</startdate><enddate>20100701</enddate><creator>Ranguelova, Kalina</creator><creator>Bonini, Marcelo G.</creator><creator>Mason, Ronald P.</creator><general>National Institute of Environmental Health Sciences</general><general>US Department of Health and Human Services</general><scope>IQODW</scope><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>3V.</scope><scope>4T-</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FE</scope><scope>8FG</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>K9-</scope><scope>K9.</scope><scope>KB0</scope><scope>L6V</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M7S</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PATMY</scope><scope>PHGZM</scope><scope>PHGZT</scope><scope>PJZUB</scope><scope>PKEHL</scope><scope>PPXIY</scope><scope>PQEST</scope><scope>PQGLB</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>Q9U</scope><scope>S0X</scope><scope>7ST</scope><scope>7TV</scope><scope>C1K</scope><scope>SOI</scope><scope>5PM</scope></search><sort><creationdate>20100701</creationdate><title>(Bi)sulfite Oxidation by Copper,Zinc-Superoxide Dismutase: Sulfite-Derived, Radical-Initiated Protein Radical Formation</title><author>Ranguelova, Kalina ; Bonini, Marcelo G. ; Mason, Ronald P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c585t-d85fed0b2bfbc1c2f7e290267abc27a3ef5a7270618c4f5045315e91192151533</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Adducts</topic><topic>Air Pollutants - metabolism</topic><topic>Anions</topic><topic>Biological and medical sciences</topic><topic>Blotting, Western</topic><topic>Chemical and industrial products toxicology. 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Perspect</addtitle><date>2010-07-01</date><risdate>2010</risdate><volume>118</volume><issue>7</issue><spage>970</spage><epage>975</epage><pages>970-975</pages><issn>0091-6765</issn><eissn>1552-9924</eissn><coden>EVHPAZ</coden><abstract>Background: Sulfur dioxide, formed during the combustion of fossil fuels, is a major air pollutant near large cities. Its two ionized forms in aqueous solution, sulfite and (bi)sulfite, are widely used as preservatives and antioxidants to prevent food and beverage spoilage. (Bi)sulfite can be oxidized by peroxidases to form the very reactive sulfur trioxide anion radical (•SO3−). This free radical further reacts with oxygen to form the peroxymonosulfate anion radical (−O3SOO•) and sulfate anion radical (SO4•−). Objective: To explore the critical role of these radical intermediates in further oxidizing biomolecules, we examined the ability of copper,zinc-superoxide dismutase (Cu,Zn-SOD) to initiate this radical chain reaction, using human serum albumin (HSA) as a model target. Methods: We used electron paramagnetic resonance, optical spectroscopy, oxygen uptake, and immuno-spin trapping to study the protein oxidations driven by sulfite-derived radicals. Results: We found that when Cu,Zn-SOD reacted with (bi)sulfite, •SO3− was produced, with the concomitant reduction of SOD-Cu(II) to SOD-Cu(I). Further, we demonstrated that sulfite oxidation mediated by Cu,Zn-SOD induced the formation of radical-derived 5,5-dimethyl-1-pyrroline N-oxide (DMPO) spin-trapped HSA radicals. Conclusions: The present study suggests that protein oxidative damage resulting from (bi)sulfite oxidation promoted by Cu,Zn-SOD could be involved in oxidative damage and tissue injury in (bi)sulfite-exacerbated allergic reactions.</abstract><cop>Research Triangle Park, NC</cop><pub>National Institute of Environmental Health Sciences</pub><pmid>20348042</pmid><doi>10.1289/ehp.0901533</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adducts Air Pollutants - metabolism Anions Biological and medical sciences Blotting, Western Chemical and industrial products toxicology. Toxic occupational diseases Chemical properties Copper in the body Cyclic N-Oxides - metabolism Electron paramagnetic resonance Electron Spin Resonance Spectroscopy Environment. Living conditions Enzyme-Linked Immunosorbent Assay Free radicals Free radicals (Chemistry) Health aspects Health savings accounts Humans Medical sciences Metals and various inorganic compounds Observations Oxidases Oxidation Oxidation-Reduction Oxidation-reduction reaction Oxidative Stress - physiology Oxygen Peroxides - metabolism Properties Public health. Hygiene Public health. Hygiene-occupational medicine Rosaniline Dyes Serum Albumin - metabolism Spectrum Analysis Spin Trapping Sulfites Sulfites - metabolism Superoxide Dismutase - metabolism Superoxides Toxicology Zinc compounds |
title | (Bi)sulfite Oxidation by Copper,Zinc-Superoxide Dismutase: Sulfite-Derived, Radical-Initiated Protein Radical Formation |
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