{"title":"光谱探针与生物大分子的相互作用:红花素t -核酸组装","authors":"Hongwen Gao, Jianfu Zhao","doi":"10.1081/TMA-120025813","DOIUrl":null,"url":null,"abstract":"Abstract The microsurface–spectral correction (MSASC) technique has been described and applied to study the assembly of safranin T on nucleic acids at pH 2.21. The formation of the electrostatic film in nucleic acids causes the aggregation of small molecules and the aggregation obeys the Langmuir isothermal adsorption. The characterization of the assembly complexes was made. Results have showed that the maximal assembly number of ST is 1.62 on each phosphate in deoxyribonucleic acid and 0.84 on each phosphate in ribonucleic acid and the binding constants of the complexes are K DNA-P-ST = 2.11 × 104 and K RNA-P-ST = 1.41 × 104 L mol−1. This aggregation was applied to the quantitative detection of nucleic acids in samples with satisfactory results.","PeriodicalId":17525,"journal":{"name":"Journal of Trace and Microprobe Techniques","volume":"24 1","pages":"615 - 625"},"PeriodicalIF":0.0000,"publicationDate":"2003-01-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"9","resultStr":"{\"title\":\"Interaction of Spectral Probe with Biomacromolecule: Safranin T-Nucleic Acid Assembly\",\"authors\":\"Hongwen Gao, Jianfu Zhao\",\"doi\":\"10.1081/TMA-120025813\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Abstract The microsurface–spectral correction (MSASC) technique has been described and applied to study the assembly of safranin T on nucleic acids at pH 2.21. The formation of the electrostatic film in nucleic acids causes the aggregation of small molecules and the aggregation obeys the Langmuir isothermal adsorption. The characterization of the assembly complexes was made. Results have showed that the maximal assembly number of ST is 1.62 on each phosphate in deoxyribonucleic acid and 0.84 on each phosphate in ribonucleic acid and the binding constants of the complexes are K DNA-P-ST = 2.11 × 104 and K RNA-P-ST = 1.41 × 104 L mol−1. This aggregation was applied to the quantitative detection of nucleic acids in samples with satisfactory results.\",\"PeriodicalId\":17525,\"journal\":{\"name\":\"Journal of Trace and Microprobe Techniques\",\"volume\":\"24 1\",\"pages\":\"615 - 625\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2003-01-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"9\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Trace and Microprobe Techniques\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1081/TMA-120025813\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Trace and Microprobe Techniques","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1081/TMA-120025813","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Interaction of Spectral Probe with Biomacromolecule: Safranin T-Nucleic Acid Assembly
Abstract The microsurface–spectral correction (MSASC) technique has been described and applied to study the assembly of safranin T on nucleic acids at pH 2.21. The formation of the electrostatic film in nucleic acids causes the aggregation of small molecules and the aggregation obeys the Langmuir isothermal adsorption. The characterization of the assembly complexes was made. Results have showed that the maximal assembly number of ST is 1.62 on each phosphate in deoxyribonucleic acid and 0.84 on each phosphate in ribonucleic acid and the binding constants of the complexes are K DNA-P-ST = 2.11 × 104 and K RNA-P-ST = 1.41 × 104 L mol−1. This aggregation was applied to the quantitative detection of nucleic acids in samples with satisfactory results.