Jockusch Steffen, Li Zengmin, Ju Jingyue, Turro Nicholas J
Department of Chemistry, Columbia University, New York, NY 10027, USA.
Photochem Photobiol. 2005 Mar-Apr;81(2):238-41. doi: 10.1562/2004-09-27-RA-329.
Two-photon excitation of a trifluorophore (6-carboxyfluorescein, N,N,N',N'-tetramethyl-6-carboxyrhodamine and cyanine-5 monofunctional dye) labeled DNA, which has a scaffold of 26 nucleotides, was achieved using focused laser light of a Q-switched Nd-YAG laser (1064 nm). The observed fluorescence signature (emission ratio from the three fluorophores) of the labeled DNA after two-photon excitation is very different from the fluorescence signatures produced by one-photon excitation at different wavelength. The additional fluorescence signatures produced by two-photon excitation of the fluorescent oligonucleotides will facilitate their use as combinatorial fluorescence energy transfer tags for multiplex genetic analysis.
使用调Q Nd-YAG激光(1064纳米)的聚焦激光对由26个核苷酸构成支架的三荧光团(6-羧基荧光素、N,N,N',N'-四甲基-6-羧基罗丹明和花菁-5单功能染料)标记的DNA进行双光子激发。双光子激发后标记DNA的观测荧光特征(三种荧光团的发射比率)与不同波长下单光子激发产生的荧光特征有很大不同。荧光寡核苷酸双光子激发产生的额外荧光特征将有助于其用作多重基因分析的组合荧光能量转移标签。