{"title":"氧自由基氧化肺表面活性剂蛋白B在水表面。","authors":"Shinichi Enami, Agustín J Colussi","doi":"10.5702/massspectrometry.S0077","DOIUrl":null,"url":null,"abstract":"<p><p>Air pollutants generate reactive oxygen species on lung surfaces. Here we report how hydroxyl radicals (·OH) injected on the surface of water react with SP-B<sub>1-25</sub>, a 25-residue polypeptide surrogate of human lung surfactant protein B. Our experiments consist of intersecting microjets of aqueous SP-B<sub>1-25</sub> solutions with O<sub>3</sub>/O<sub>2</sub>/H<sub>2</sub>O/N<sub>2</sub>(g) gas streams that are photolyzed into ·OH(g) <i>in situ</i> by 266 nm laser nanosecond pulses. Surface-sensitive mass spectrometry enables us to monitor the prompt (<10 μs) and simultaneous formation of primary O <i><sub>n</sub></i> -containing products/intermediates (<i>n</i>≤5) triggered by the reaction of ·OH with interfacial SP-B<sub>1-25</sub>. We found that O-atoms from both O<sub>3</sub> and ·OH are incorporated into the reactive cysteine Cys<sub>8</sub> and Cys<sub>11</sub> and tryptophan Trp<sub>9</sub> components of the hydrophobic N-terminus of SP-B<sub>1-25</sub> that lies at the topmost layers of the air-liquid interface. Remarkably, these processes are initiated by ·OH additions rather than by H-atom abstractions from S-H, C-H, or N-H groups. By increasing the hydrophilicity of the N-terminus region of SP-B<sub>1-25</sub>, these transformations will impair its role as a surfactant.</p>","PeriodicalId":18243,"journal":{"name":"Mass spectrometry","volume":"7 2","pages":"S0077"},"PeriodicalIF":0.0000,"publicationDate":"2018-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.5702/massspectrometry.S0077","citationCount":"3","resultStr":"{\"title\":\"OH-Radical Oxidation of Lung Surfactant Protein B on Aqueous Surfaces.\",\"authors\":\"Shinichi Enami, Agustín J Colussi\",\"doi\":\"10.5702/massspectrometry.S0077\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Air pollutants generate reactive oxygen species on lung surfaces. Here we report how hydroxyl radicals (·OH) injected on the surface of water react with SP-B<sub>1-25</sub>, a 25-residue polypeptide surrogate of human lung surfactant protein B. Our experiments consist of intersecting microjets of aqueous SP-B<sub>1-25</sub> solutions with O<sub>3</sub>/O<sub>2</sub>/H<sub>2</sub>O/N<sub>2</sub>(g) gas streams that are photolyzed into ·OH(g) <i>in situ</i> by 266 nm laser nanosecond pulses. Surface-sensitive mass spectrometry enables us to monitor the prompt (<10 μs) and simultaneous formation of primary O <i><sub>n</sub></i> -containing products/intermediates (<i>n</i>≤5) triggered by the reaction of ·OH with interfacial SP-B<sub>1-25</sub>. We found that O-atoms from both O<sub>3</sub> and ·OH are incorporated into the reactive cysteine Cys<sub>8</sub> and Cys<sub>11</sub> and tryptophan Trp<sub>9</sub> components of the hydrophobic N-terminus of SP-B<sub>1-25</sub> that lies at the topmost layers of the air-liquid interface. Remarkably, these processes are initiated by ·OH additions rather than by H-atom abstractions from S-H, C-H, or N-H groups. By increasing the hydrophilicity of the N-terminus region of SP-B<sub>1-25</sub>, these transformations will impair its role as a surfactant.</p>\",\"PeriodicalId\":18243,\"journal\":{\"name\":\"Mass spectrometry\",\"volume\":\"7 2\",\"pages\":\"S0077\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2018-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.5702/massspectrometry.S0077\",\"citationCount\":\"3\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Mass spectrometry\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.5702/massspectrometry.S0077\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2018/11/21 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q3\",\"JCRName\":\"Physics and Astronomy\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Mass spectrometry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5702/massspectrometry.S0077","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2018/11/21 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"Physics and Astronomy","Score":null,"Total":0}
OH-Radical Oxidation of Lung Surfactant Protein B on Aqueous Surfaces.
Air pollutants generate reactive oxygen species on lung surfaces. Here we report how hydroxyl radicals (·OH) injected on the surface of water react with SP-B1-25, a 25-residue polypeptide surrogate of human lung surfactant protein B. Our experiments consist of intersecting microjets of aqueous SP-B1-25 solutions with O3/O2/H2O/N2(g) gas streams that are photolyzed into ·OH(g) in situ by 266 nm laser nanosecond pulses. Surface-sensitive mass spectrometry enables us to monitor the prompt (<10 μs) and simultaneous formation of primary O n -containing products/intermediates (n≤5) triggered by the reaction of ·OH with interfacial SP-B1-25. We found that O-atoms from both O3 and ·OH are incorporated into the reactive cysteine Cys8 and Cys11 and tryptophan Trp9 components of the hydrophobic N-terminus of SP-B1-25 that lies at the topmost layers of the air-liquid interface. Remarkably, these processes are initiated by ·OH additions rather than by H-atom abstractions from S-H, C-H, or N-H groups. By increasing the hydrophilicity of the N-terminus region of SP-B1-25, these transformations will impair its role as a surfactant.