Malicka Joanna, Gryczynski Ignacy, Gryczynski Zygmunt, Lakowicz Joseph R
Center for Fluorescence Spectroscopy, Department of Biochemistry and Molecular Biology, University of Maryland at Baltimore, 725 West Lombard Street, Baltimore, Maryland 21201, USA.
Anal Chem. 2003 Dec 1;75(23):6629-33. doi: 10.1021/ac034881e.
We describe a new approach to measuring DNA hybridization using surface plasmon-coupled emission (SPCE). Excited fluorophores are known to couple with surface oscillations of electrons in thin metal films, typically 50 nm thick silver on a glass prism. These surface plasmons then radiate into the glass at a sharply defined angle determined by the emission wavelength and the optical properties of the glass and metal. This radiation has the same spectral profile as the emission spectrum of the fluorophores. We studied the emission due to Cy3-labeled DNA oligomers bound to complementary unlabeled oligomers which were themselves bound to the metal surface. Hybridization resulted in SPCE due to Cy3-DNA into the prism. Directional SPCE was observed whether the sample was illuminated from the sample side or through the glass substrate at the surface plasmon angle for the excitation wavelength. A large fraction of the total potential emission is coupled to the surface plasmons resulting in improved sensitivity. When illuminated through the prism at the surface plasmon angle, the sensitivity is increased due to the enhanced intensity of the resonance evanescent field. It is known that SPCE depends on proximity to the silver surface. As a result, changes in emission intensity are observed due to fluorophore localization even if hybridization does not affect the quantum yield of the fluorophore. The use of SPCE resulted in suppression of interfering emission from a noncomplementary Cy5-DNA oligomers due to weaker coupling of the more distant fluorophores with the surface plasmons. We expect SPCE to have numerous applications to nucleic acid analysis and for the measurement of bioaffinity reactions.
我们描述了一种使用表面等离子体耦合发射(SPCE)来测量DNA杂交的新方法。已知受激发的荧光团会与薄金属膜(通常是玻璃棱镜上50纳米厚的银膜)中电子的表面振荡耦合。这些表面等离子体随后以由发射波长以及玻璃和金属的光学性质所确定的锐定义角度辐射到玻璃中。这种辐射具有与荧光团发射光谱相同的光谱轮廓。我们研究了与互补的未标记寡聚物结合的Cy3标记的DNA寡聚物的发射情况,这些未标记寡聚物本身结合在金属表面。杂交导致Cy3-DNA产生SPCE并进入棱镜。无论样品是从样品侧照射还是以激发波长的表面等离子体角度通过玻璃基板照射,都观察到了定向SPCE。总潜在发射的很大一部分与表面等离子体耦合,从而提高了灵敏度。当以表面等离子体角度通过棱镜照射时,由于共振倏逝场强度的增强,灵敏度会提高。已知SPCE取决于与银表面的接近程度。因此,即使杂交不影响荧光团的量子产率,由于荧光团的定位也会观察到发射强度的变化。使用SPCE可抑制来自非互补Cy5-DNA寡聚物的干扰发射,因为距离较远的荧光团与表面等离子体的耦合较弱。我们预计SPCE在核酸分析以及生物亲和反应测量方面有众多应用。