Zhang Jian, Fu Yi, Lakowicz Joseph R
Center for Fluorescence Spectroscopy, University of Maryland School of Medicine, Department of Biochemistry and Molecular Biology, 725 West Lombard Street, Baltimore, Maryland 21201, USA.
Langmuir. 2007 Nov 6;23(23):11734-9. doi: 10.1021/la702064v. Epub 2007 Oct 3.
Oligonucleotide-bound silver particles were coupled through hybridization with target complementary oligonucleotides. YOYO molecules were intercalated into DNA duplexes bound between the coupled metal particles. Fluorescence images of YOYO molecules were monitored by scanning confocal microscopy. Relative to the free single YOYO, the emission brightness of the image was enhanced 80-fold after intercalating the fluorophores into the DNA duplexes between the coupled silver particles. Some images of the labeled metal particle dimers were observed to be dumbbell-shaped, suggesting that the stretching of intercalated YOYO molecules was restricted because of the orientation effect of fluorophores. The shortened lifetime of YOYO molecules between the coupled metal particles indicated that the fluorescence was enhanced via a near-field interaction mechanism between the fluorophore and the metal nanoparticle.
通过与靶标互补寡核苷酸杂交,使结合了寡核苷酸的银颗粒相互偶联。YOYO分子插入到偶联金属颗粒之间结合的DNA双链体中。通过扫描共聚焦显微镜监测YOYO分子的荧光图像。相对于游离的单个YOYO,将荧光团插入偶联银颗粒之间的DNA双链体后,图像的发射亮度增强了80倍。观察到一些标记的金属颗粒二聚体的图像呈哑铃状,这表明由于荧光团的取向效应,插入的YOYO分子的伸展受到限制。偶联金属颗粒之间的YOYO分子寿命缩短,表明荧光是通过荧光团与金属纳米颗粒之间的近场相互作用机制增强的。