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Determination of Nucleic Acids Using Calcein-Neodymium Complex as a Fluorescence Probe

机译:钙黄绿素-钕络合物作为荧光探针测定核酸

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摘要

A novel fluorometric method has been developed for rapid determination of DNA and RNA with calcein-neodymium complex as a fluorescence probe. The method is based on the fluorescence enhancement of calcein-Nd(III) complex in the presence of DNA or RNA, with maximum excitation and emission wavelength at 489 nm and 514 nm, respectively. Under optimal conditions, the calibration graphs are linear over the range 0.5 - 3.0 μg/ml for both DNA and yeast RNA, 0.4 - 2.0 μg/ml for fish sperm DNA (FS DNA) and 0 - 3.0 μg/ml for calf thymus DNA (CT DNA). The corresponding detection limits are 15.1 ng/ml for DNA, 21.2 ng/ml for yeast RNA, 10.5 ng/ml for FS DNA and 8.9 ng/ml for CT DNA. The interaction mechanism for the binding of calcein-Nd(III) complex to DNA is also studied. The results of absorption spectra, fluorescence polarization measurements and thermal denaturation experiments, suggested that the interaction between calcein-Nd(III) complex and DNA is an electrostatic interaction.
机译:已经开发出一种新颖的荧光测定方法,以钙黄绿素-钕络合物为荧光探针快速测定DNA和RNA。该方法基于钙黄绿素-Nd(III)复合物在DNA或RNA存在下的荧光增强,最大激发和发射波长分别在489 nm和514 nm。在最佳条件下,DNA和酵母RNA的校正曲线在0.5-3.0μg/ ml范围内呈线性,鱼精DNA(FS DNA)的校正曲线在0.4-2.0μg/ ml范围内,小胸腺DNA的校正曲线在0-3.0μg/ ml范围内(CT DNA)。相应的检测限为:DNA的15.1 ng / ml,酵母RNA的21.2 ng / ml,FS DNA的10.5 ng / ml和CT DNA的8.9 ng / ml。还研究了钙黄绿素-Nd(III)复合物与DNA结合的相互作用机理。吸收光谱,荧光偏振测量和热变性实验的结果表明,钙黄绿素-Nd(III)配合物与DNA之间的相互作用是静电相互作用。

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