Holzapfel Hadassa Y, Birtwistle Marc R
Department of Pharmacology and Systems Therapeutics | Icahn School of Medicine at Mount Sinai | New York, NY, USA.
Transl Sci. 2016 Mar;2(3). Epub 2016 Mar 31.
Fluorescently-labeled antibodies are central to many biochemical assays, but they are not easy to multiplex beyond 3-4 colors. A long-term hypothesis of ours is that labeling antibodies with multiple fluorophores, in a way such that fluorescence resonance energy transfer (FRET) occurs, may provide a way to increase fluorescence multiplexing ability by creating a rich variety of complex emission spectra that could be deconvolved via spectral methods. However, it is not yet clear how one can effectively label antibodies with multiple fluorophores that exhibit FRET. Here, we show how to use Mix-n-Stain antibody labeling kits from Biotium to label antibodies with multiple fluorophores that exhibit FRET. Key to our approach is the use of Fab fragments, as opposed to full IgG molecules, since the full IgG molecules are generally too large to allow the fluorophore proximity necessary for observable FRET. We show that our approach works with two different sets of FRET-capable fluorophore combinations: CF405M/CF488A and CF568/CF640R. These results form the basis for continued development of approaches for increased multiplexing of fluorescent antibody measurements.
荧光标记抗体是许多生化检测的核心,但要实现超过3 - 4种颜色的多重检测并不容易。我们长期以来的一个假设是,以一种能发生荧光共振能量转移(FRET)的方式用多种荧光团标记抗体,可能会通过创建丰富多样的复杂发射光谱来提供一种提高荧光多重检测能力的方法,这些光谱可通过光谱方法进行解卷积。然而,目前尚不清楚如何用能表现出FRET的多种荧光团有效地标记抗体。在这里,我们展示了如何使用Biotium公司的Mix - n - Stain抗体标记试剂盒,用能表现出FRET的多种荧光团来标记抗体。我们方法的关键在于使用Fab片段,而不是完整的IgG分子,因为完整的IgG分子通常太大,无法实现可观察到FRET所需的荧光团接近程度。我们表明我们的方法适用于两组不同的具有FRET能力的荧光团组合:CF405M/CF488A和CF568/CF640R。这些结果为持续开发增加荧光抗体检测多重性的方法奠定了基础。