A fluorescent flavonoid for lysosome detection in live cells under "wash free'' conditions

被引:25
作者
Bertman, Keti Assor [1 ]
Abeywickrama, Chathura S. [1 ]
Baumann, Hannah J. [1 ]
Alexander, Nicolas [1 ]
McDonald, Lucas [1 ]
Shriver, Leah P. [1 ,2 ,3 ]
Konopka, Michael [1 ]
Pang, Yi [1 ,4 ]
机构
[1] Univ Akron, Dept Chem, Akron, OH 44325 USA
[2] Dept Biol, Akron, OH 44325 USA
[3] Univ Akron, Akron, OH 44325 USA
[4] Univ Akron, Maurice Marton Inst Polymer Sci, Akron, OH 44325 USA
关键词
LARGE STOKES SHIFT; PH CHANGES; PROBE; MECHANISMS;
D O I
10.1039/c8tb00325d
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
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 (Delta lambda < 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 (phi(fl) 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 approximate to 50 mu M.
引用
收藏
页码:5050 / 5058
页数:9
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