Wahlroos Rina, Toivonen Juha, Tirri Marko, Hänninen Pekka
Laboratory of Biophysics, Institute of Biomedicine, University of Turku, P.O. Box 123, 20521 Turku, Finland.
J Fluoresc. 2006 May;16(3):379-86. doi: 10.1007/s10895-006-0084-x. Epub 2006 May 16.
The use of two-photon excitation of fluorescence for detection of fluorescence resonance energy transfer (FRET) was studied for a selected fluorescent donor-acceptor pair. A method based on labeled DNA was developed for controlling the distance between the donor and the acceptor molecules. The method consists of hybridization of fluorescent oligonucleotides to a complementary single-stranded target DNA. As the efficiency of FRET is strongly distance dependent, energy transfer does not occur unless the fluorescent oligonucleotides and the target DNA are hybridized. A high degree of DNA hybridization and an excellent FRET efficiency were verified with one-photon excited fluorescence studies. Excitation spectra of fluorophores are usually wider in case of two-photon excitation than in the case of one-photon excitation. This makes the selective excitation of donor difficult and might cause errors in detection of FRET with two-photon excited fluorescence. Different techniques to analyze the FRET efficiency from two-photon excited fluorescence data are discussed. The quenching of the donor fluorescence intensity turned to be the most consistent way to detect the FRET efficiency. The two-photon excited FRET is shown to give a good response to the distance between the donor and the acceptor molecules.
针对选定的荧光供体 - 受体对,研究了利用双光子激发荧光来检测荧光共振能量转移(FRET)。开发了一种基于标记DNA的方法来控制供体和受体分子之间的距离。该方法包括将荧光寡核苷酸与互补的单链靶DNA杂交。由于FRET效率强烈依赖于距离,除非荧光寡核苷酸与靶DNA杂交,否则不会发生能量转移。通过单光子激发荧光研究验证了高度的DNA杂交和优异的FRET效率。在双光子激发的情况下,荧光团的激发光谱通常比单光子激发时更宽。这使得供体的选择性激发变得困难,并且可能在双光子激发荧光检测FRET时导致误差。讨论了从双光子激发荧光数据中分析FRET效率的不同技术。供体荧光强度的猝灭被证明是检测FRET效率最一致的方法。双光子激发FRET对供体和受体分子之间的距离显示出良好的响应。