Huang Cheng Zhi, Liao Qie Gen, Li Yuan Fang
College of Pharmaceutical Sciences, CQKL-LRTA, Southwest University, Chongqing 400715, China.
Talanta. 2008 Mar 15;75(1):163-6. doi: 10.1016/j.talanta.2007.10.049. Epub 2007 Nov 9.
With water-soluble anionic tetra (p-carboxyphenyl) porphyrin (TCPP) to solubilize multi-walled carbon nanotubes (MCNTs), we obtained a suspension that could be stable more than 1 week. With this TCPP/MCNTs suspension, we propose a spectrofluorometric method of DNA hybridization in this contribution. Our basic finding for this work is that the fluorescence from a dye-tagged single stranded DNA (ssDNA), which was directly added to the TCPP/MCNTs suspension, gets quenched, and the fluorescence could be remained if the dye-tagged single stranded DNA is first to be hybridized with its complementary target DNA to form a double stranded DNA (dsDNA) hybrid and added into the TCPP/MCNTs suspension. Mechanism investigations showed that the reason for the former is due to the adsorption of ssDNA on the surfaces of MCNTs, and that for the latter is due to the strong electrostatic repulsion force between the negative charge TCPP/MCNTs complexes and dsDNA. Thus, target DNA in a DNA sample and single-base mismatch in DNA sequences could be easily detected.
通过用水溶性阴离子四(对羧基苯基)卟啉(TCPP)增溶多壁碳纳米管(MCNT),我们获得了一种可稳定超过1周的悬浮液。在本论文中,利用这种TCPP/MCNT悬浮液,我们提出了一种用于DNA杂交的荧光光谱法。这项工作的基本发现是,直接添加到TCPP/MCNT悬浮液中的染料标记单链DNA(ssDNA)的荧光会猝灭,而如果先将染料标记单链DNA与其互补靶DNA杂交形成双链DNA(dsDNA)杂交体,再添加到TCPP/MCNT悬浮液中,则荧光会保留。机理研究表明,前者是由于ssDNA吸附在MCNT表面,而后者是由于带负电荷的TCPP/MCNT复合物与dsDNA之间的强静电斥力。因此,可以轻松检测DNA样品中的靶DNA和DNA序列中的单碱基错配。