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Light up Live Cell Nuclear Envelope in Real-Time Using a Two-Photon Absorption and AIE Chromophore

机译:使用双光子吸收和AIE发色团实时点亮活细胞核包膜

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摘要

In this letter, aggregation from two-photon absorption (2PA) molecules in living cells were firstly observed and the related aggregation induced emission (AIE) properties were investigated as a cell tracer for L ((Z)-3-(4-(Bis(4-ethoxyphenyl) amino)phenyl)-2-(4-amino-phenyl)- acrylonitrile cyano-substituted ) based on triphenylamine with D-pi-A model. L was further used as a two-photon absorption (2PA, lambda(ex) = 900, lambda(em) = 550 nm delta = 156 GM) live-cell marker for real-time, long-term cell growth and proliferation monitoring, with rapidly adhering whole intracellular membrane-rich system. Remarkably, different from existing organic AIE chromophores and other commercially available probes, L exhibited intense intracellular-AIE property with stable nuclear envelope (NE) staining under two-photon excited microscopy (TPEM) through detailed in cellulo studies.
机译:在这封信中,首先观察到活细胞中双光子吸收(2PA)分子的聚集,并研究了相关的聚集诱导发射(AIE)特性作为L((Z)-3-(4-(Bis基于三苯胺的具有D-pi-A模型的(4-乙氧基苯基)氨基)苯基)-2-(4-氨基-苯基)-丙烯腈氰基取代的)。 L进一步用作双光子吸收(2PA,lambda(ex)= 900,lambda(em)= 550 nm delta = 156 GM)活细胞标记,用于实时,长期细胞生长和增殖监测,与快速粘附整个细胞内膜丰富的系统。值得注意的是,与现有的有机AIE生色团和其他市售探针不同,在纤维素研究中,L在双光子激发显微镜(TPEM)下表现出强烈的细胞内AIE特性和稳定的核被膜(NE)染色。

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