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来自异质等离子体纳米结构的藻胆蛋白的金属增强荧光

Metal-Enhanced Fluorescence of Phycobiliproteins from Heterogeneous Plasmonic Nanostructures.

作者信息

Chowdhury Mustafa H, Ray Krishanu, Aslan Kadir, Lakowicz Joseph R, Geddes Chris D

机构信息

Center for Fluorescence Spectroscopy, Medical Biotechnology Center, University of Maryland School of Medicine, 725 West Lombard Street, Baltimore, Maryland 21201, and Institute of Fluorescence, Laboratory for Advanced Medical Plasmonics, & Laboratory for Advanced Fluorescence Spectroscopy, Medical Biotechnology Center, University of Maryland Biotechnology Institute, 725 West Lombard Street, Baltimore, Maryland 21201.

出版信息

J Phys Chem C Nanomater Interfaces. 2007 Dec 5;111(51):18856-18863. doi: 10.1021/jp0731250.

Abstract

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.

摘要

我们在此报告了以银岛膜(SiFs)形式存在的等离子体金属纳米结构用于增强五种不同藻胆蛋白荧光发射的情况。我们的研究结果清楚地表明,与组装在对照样品胺基封端玻璃载玻片表面的单层藻胆蛋白相比,当藻胆蛋白在SiFs上方组装成单层时,其荧光发射强度最多可增加9倍,寿命最多可缩短7倍。该研究还在夹在一起的两个玻璃基板(以及一个SiFs和一个玻璃基板)之间夹有藻胆蛋白薄液层的情况下重复进行。同样,结果表明,与玻璃对照样品相比,在SiF - 玻璃设置中藻胆蛋白的荧光发射强度最多可增加10倍,寿命缩短2倍,这意味着无论蛋白质与SiFs有无化学连接,都可以实现藻胆蛋白发射的近场增强。因此,我们的结果清楚地表明,金属增强荧光(MEF)有可能用于提高大量使用藻胆蛋白作为荧光标记的生物测定的灵敏度和检测限,例如在可以连接到SiFs表面的荧光免疫测定中,以及在液相分析物可能流经涂有SiFs的通道而实际上不附着在银上的流式细胞术中。

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