Laboratoire de Conception et Application de Molécules Bioactives, UMR 7199 CNRS, Faculté de Pharmacie, Université de Strasbourg, 74 Route du Rhin 67401 Illkirch Cédex, France.
J Am Chem Soc. 2010 Mar 3;132(8):2585-90. doi: 10.1021/ja9074562.
Total synthesis and photophysical properties of PENB-DDAO, a photoactivatable 1,3-dichloro-9,9-dimethyl-9H-acridin-2(7)-one (DDAO) derivative of a far-red emitting fluorophore, are described. The photoremovable group of the DDAO phenolic function comprises a donor/acceptor biphenyl platform which allows an efficient (> or = 95%) and rapid (< 15 micros time-range) release of the fluorescent signal and displays remarkable two-photon uncaging cross sections (delta(a) x Phi(u) = 3.7 GM at 740 nm). PENB-DDAO is cell permeable as demonstrated by the triggering of cytoplasmic red fluorescent signal in HeLa cells after one-photon irradiation (lambda(exc) around 360 nm) or by the generation of a red fluorescent signal in a delineated area of a single cell after two-photon photoactivation (lambda(exc) = 770 nm).
PENB-DDAO 的全合成及光物理性质研究,一种远红发射荧光团的光激活 1,3-二氯-9,9-二甲基-9H-吖啶-2(7)-酮(DDAO)衍生物。DDAO 酚基功能的光可去除基团包含供体/受体联苯平台,其允许高效(>或= 95%)和快速(<15 微秒时间范围)释放荧光信号,并显示出显著的双光子无笼化横截面(在 740nm 处 delta(a) x Phi(u) = 3.7 GM)。PENB-DDAO 具有细胞通透性,这可通过 HeLa 细胞中细胞质红色荧光信号的单光子照射(激发波长约 360nm)触发或通过双光子光激活后在单个细胞的划定区域中产生红色荧光信号来证明(激发波长 = 770nm)。