Bertman Keti Assor, Abeywickrama Chathura S, Baumann Hannah J, Alexander Nicolas, McDonald Lucas, Shriver Leah P, Konopka Michael, Pang Yi
Department of Chemistry, University of Akron, Akron, Ohio 44325, USA.
J Mater Chem B. 2018 Aug 21;6(31):5050-5058. doi: 10.1039/c8tb00325d. Epub 2018 Jul 24.
Lysosomes are vital organelles in living cells, which have acidic environments (pH 4.0-5.0) where macrobiomolecules and malfunctioning organelles are broken down into monomers by hydrolase activity. The majority of the currently reported fluorescent probes for detecting lysosomes suffer from small Stokes shifts (Δλ < 20 nm) and higher cytotoxicity due to an "alkalinizing effect". An interesting flavonoid-based lysosome probe is synthesized by introducing a morpholine moiety onto the flavonoid skeleton. This new probe has shown excellent selectivity to detect lysosomes in MO3.13 oligodendrocytes and normal human lung fibroblast cell lines. Probes 1a and 1b have shown excellent fluorescence quantum yield (φ up to 0.43 in non-aqueous solvents) and large Stokes shifts (120-150 nm). These new fluorescent probes also exhibit a large quantum yield difference from an aqueous to organic environment, making them potentially useful as "wash-free" stains for visualizing lysosomes. Cell viability evaluation of these probes shows excellent biocompatibility with the median lethal concentration being LC50 ≈ 50 μM.
溶酶体是活细胞中的重要细胞器,其内部环境呈酸性(pH 4.0 - 5.0),在这种环境下,大分子生物物质和功能失调的细胞器通过水解酶的活性被分解为单体。目前报道的大多数用于检测溶酶体的荧光探针由于“碱化效应”,斯托克斯位移较小(Δλ < 20 nm)且细胞毒性较高。通过在黄酮骨架上引入吗啉部分,合成了一种有趣的基于黄酮的溶酶体探针。这种新探针在检测MO3.13少突胶质细胞和正常人肺成纤维细胞系中的溶酶体时表现出优异的选择性。探针1a和1b表现出优异的荧光量子产率(在非水溶剂中φ高达0.43)和较大的斯托克斯位移(120 - 150 nm)。这些新型荧光探针在从水性环境到有机环境时还表现出较大的量子产率差异,使其有可能作为“免洗”染料用于溶酶体成像。对这些探针的细胞活力评估显示出优异的生物相容性,其半数致死浓度LC50≈50 μM。