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基于亚甲基蓝与DNA相互作用的DNA同步荧光测定法。

Synchronous fluorescence determination of DNA based on the interaction between methylene blue and DNA.

作者信息

Hu Zhou, Tong Changlun

机构信息

Institute of Environmental Science, Zhejiang University, Hangzhou 310029, China.

出版信息

Anal Chim Acta. 2007 Mar 28;587(2):187-93. doi: 10.1016/j.aca.2007.01.050. Epub 2007 Jan 25.

Abstract

The fluorescence intensity of methylene blue (MB) quenched by DNA in the pH range of 6.5-8.0 was studied with synchronous fluorescence technology. A novel method for detecting single-stranded and double-stranded DNA was developed. The decreased fluorescence intensity at 664 nm is in proportion to the concentration of DNA in the range of 0.28-11.0 micromol L(-1) for ctDNA, 0.14-8.25 micromol L(-1) for thermally denatured ctDNA and 0.28-8.25 micromol L(-1) for hsDNA. The detection limits (S/N=3) are 0.11, 0.04 and 0.04 micromol L(-1), respectively. The method is rapid, selective, and the reagents are lower toxic. It has been used for the determination of DNA in synthetic samples with good satisfaction. In addition, the interaction modes between MB and ctDNA and the mechanism of the fluorescence quenching were also discussed in detail. The experimental results from absorption spectra and fluorescence polarization indicate that the possible interaction modes between MB and DNA are the electrostatic binding and the intercalation binding.

摘要

采用同步荧光技术研究了在pH值为6.5 - 8.0范围内DNA对亚甲基蓝(MB)荧光强度的猝灭作用。开发了一种检测单链和双链DNA的新方法。对于小牛胸腺DNA(ctDNA),在664 nm处荧光强度的降低与DNA浓度在0.28 - 11.0 μmol L⁻¹范围内成正比;对于热变性的ctDNA,在0.14 - 8.25 μmol L⁻¹范围内成正比;对于人血清白蛋白DNA(hsDNA),在0.28 - 8.25 μmol L⁻¹范围内成正比。检测限(S/N = 3)分别为0.11、0.04和0.04 μmol L⁻¹。该方法快速、具有选择性,且试剂毒性较低。已用于合成样品中DNA的测定,结果令人满意。此外,还详细讨论了MB与ctDNA之间的相互作用模式以及荧光猝灭的机理。吸收光谱和荧光偏振的实验结果表明,MB与DNA之间可能的相互作用模式是静电结合和嵌入结合。

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