Jena Sampreeti, Damayanti Nur P, Tan Jackie, Pratt Erica D, Irudayaraj Joseph M K, Parker Laurie L
Department of Biochemistry, Molecular Biology and Biophysics, Masonic Cancer Center, University of Minnesota, Minneapolis, 55455, USA.
Chem Commun (Camb). 2020 Nov 11;56(87):13409-13412. doi: 10.1039/d0cc05030j. Epub 2020 Oct 9.
Many commonly employed strategies to map kinase activities in live cells require expression of genetically encoded proteins (e.g. FRET sensors). In this work, we describe the development and preliminary application of a set of cell-penetrating, fluorophore labelled peptide substrates for fluorescence lifetime imaging (FLIM) of Abl and Src-family kinase activities. These probes do not rely on FRET pairs or genetically-encoded protein expression. We further demonstrate probe multiplexing and pixel-by-pixel quantification to estimate the relative proportion of modified probe, suggesting that this strategy will be useful for detailed mapping of single cell and subcellular dynamics of multiple kinases concurrently in live cells.
许多用于在活细胞中绘制激酶活性图谱的常用策略都需要表达基因编码蛋白(例如FRET传感器)。在这项工作中,我们描述了一组用于Abl和Src家族激酶活性荧光寿命成像(FLIM)的细胞穿透性、荧光团标记的肽底物的开发和初步应用。这些探针不依赖于FRET对或基因编码蛋白的表达。我们进一步展示了探针复用和逐像素定量,以估计修饰探针的相对比例,这表明该策略将有助于在活细胞中同时详细绘制多种激酶的单细胞和亚细胞动力学图谱。