Metal-enhanced fluorescence of phycobiliproteins from heterogeneous plasmonic nanostructures

被引:48
作者
Chowdhury, Mustafa H. [2 ]
Ray, Krishanu
Aslan, Kadir
Lakowicz, Joseph R. [2 ]
Geddes, Chris D. [1 ]
机构
[1] Univ Maryland, Inst Biotechnol, Ctr Med Biotechnol, Lab Adv Fluorescence Spectroscopy,Lab Adv Med Pla, Baltimore, MD 21201 USA
[2] Univ Maryland, Sch Med, Ctr Med Biotechnol, Ctr Fluorescence Spectroscopy, Baltimore, MD 21201 USA
关键词
D O I
10.1021/jp0731250
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We report here the use of plasmonic metal nanostructures in the form of silver island films (SiFs) to enhance the fluorescence emission of five different phycobiliproteins. Our findings clearly show that the phycobiliproteins display up to a 9-fold increase in fluorescence emission intensity, with a maximum 7-fold decrease in lifetime when they are assembled as a monolayer above SiFs, as compared to a monolayer assembled on the surface of amine-terminated glass slides of the control sample. The study was also repeated with a thin liquid layer of the phycobiliproteins sandwiched between two glass substrates (and a SiFs and a glass substrate) clamped together. Similarly, the results show a maximum 10-fold increase in fluorescence emission intensity coupled with a 2-fold decrease in lifetime of the phycobiliproteins in the SiF-glass setup as compared to the glass control sample, implying that near-field enhancement of phycobiliprotein emission can be attained both with and without chemical linkage of the proteins to the SiFs. Hence, our results clearly show that metal-enhanced fluorescence (MEF) can potentially be employed to increase the sensitivity and detection limit of the plethora of bioassays that employ phycobiliproteins as fluorescence labels, such as in fluoro-immunoassays where the assay can be tethered on the surface of SiFs, and also in flow cytometry where analytes in the liquid phase could potentially flow through channels coated with SiFs without actually being attached to the silver.
引用
收藏
页码:18856 / 18863
页数:8
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