A simple spectrophotometric streptavidin-biotin binding assay utilizing biotin-4-fluorescein

被引:20
作者
Waner, Mark J. [1 ]
Mascotti, David P. [1 ]
机构
[1] John Carroll Univ, Dept Chem, University Hts, OH 44118 USA
来源
JOURNAL OF BIOCHEMICAL AND BIOPHYSICAL METHODS | 2008年 / 70卷 / 06期
关键词
streptavidin; biotin; biotin-4-fluorescein; absorbance; extinction coefficient; spectrophotometric assay;
D O I
10.1016/j.jbbm.2007.06.001
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A new assay for biotin binding capacity of Streptavidin (SA) is presented in this work. The assay is based on the large decrease in the extinction coefficient at 493 nm that accompanies binding of biotin-4-fluorescein (B4F) to SA. This decrease is attributed to formation of a charge transfer complex between the B4F-donor and one or more SA residues. We show that one may observe the stoichiometric binding via monitoring the absorbance at 493 nm using either SA or B4F as the titrant. The sensitivity of the assay is at the lower end of similar fluorimetric and photometric assays. Though the sensitivity is not substantially lower than other comparable techniques, this assay allows one added flexibility in working range and instrumentation, since the same stock solutions may be used for this new photometric assay or the fluorescence assay for which this ligand was first developed. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:873 / 877
页数:5
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2007, PROZYME STREPTAVIDIN