光谱探针与生物大分子的相互作用:红花素t -核酸组装

Hongwen Gao, Jianfu Zhao
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引用次数: 9

摘要

摘要采用微表面光谱校正(MSASC)技术研究了pH为2.21时藏红花苷T在核酸上的组装。核酸中静电膜的形成使小分子聚集,聚集服从朗缪尔等温吸附。对组装配合物进行了表征。结果表明,DNA-P-ST在脱氧核糖核酸每个磷酸基上的最大组装数为1.62,在核糖核酸每个磷酸基上的最大组装数为0.84,配合物的结合常数为K DNA-P-ST = 2.11 × 104和K RNA-P-ST = 1.41 × 104 L mol−1。该聚合体应用于样品中核酸的定量检测,结果令人满意。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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.
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