Waner Mark J, Mascotti David P
Department of Chemistry, John Carroll University, 20700 North Park Blvd., University Heights, OH 44118 USA.
J Biochem Biophys Methods. 2008 Apr 24;70(6):873-7. doi: 10.1016/j.jbbm.2007.06.001. Epub 2007 Jul 4.
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.
本研究提出了一种新的链霉亲和素(SA)生物素结合能力测定方法。该测定方法基于生物素 - 4 - 荧光素(B4F)与SA结合时在493nm处消光系数的大幅降低。这种降低归因于B4F供体与一个或多个SA残基之间形成了电荷转移复合物。我们表明,使用SA或B4F作为滴定剂,通过监测493nm处的吸光度,可以观察到化学计量结合。该测定方法的灵敏度处于类似荧光和光度测定方法的较低水平。尽管灵敏度并不比其他可比技术低很多,但这种测定方法在工作范围和仪器使用方面提供了额外的灵活性,因为相同的储备溶液可用于这种新的光度测定方法或该配体最初开发的荧光测定方法。