Fluoroprofile, a fluorescence-based assay for rapid and sensitive quantitation of proteins in solution

被引:24
作者
Mackintosh, JA
Veal, DA
Karuso, P [1 ]
机构
[1] Macquarie Univ, Dept Chem & Biomol Sci, N Ryde, NSW 2109, Australia
[2] FLUOROtech Pty Ltd, Sydney, NSW, Australia
关键词
2-DE; epicocconone; fluorescence; protein quantitation;
D O I
10.1002/pmic.200500095
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The development of a sensitive fluorescence-based assay for the quantitative determination of protein concentration is described. The assay is based on the natural product epicocconone, which produces a large increase in fluorescence quantum yield upon binding to detergent-coated proteins in solution. There is a concomitant shift in the emission maximum from 520 to 605 nm after binding, which results in low background signal allowing a linear dynamic range of 40 ng/ mL to 200 mu g/ml, for most proteins. There is little protein-to-protein variation except for iron-containing proteins and the assay can be used so that it is tolerant of chemicals commonly used in 2-D sample buffers. The assay is more sensitive than standard absorption assays such as the Bradford and Lowry assays, and has a greater dynamic range and sensitivity than other fluorescent assays.
引用
收藏
页码:4673 / 4677
页数:5
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