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首页> 外文期刊>ACS nano >Intracellular delivery of bioactive molecules using light-addressable nanocapsules
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Intracellular delivery of bioactive molecules using light-addressable nanocapsules

机译:使用光寻址纳米胶囊在细胞内传递生物活性分子

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摘要

This paper describes a method by which molecules that are impermeable to cells are encapsulated in dye-sensitized lipid nanocapsules for delivery into cells via endocytosis. Once inside the cells, the molecules are released from the lipid nanocapsules into the cytoplasm with a single nanosecond pulse from a laser in the far red (645 nm). We demonstrate this method with the intracellular release of the second messenger IP3 in CHO-M1 cells and report that calcium responses from the cells changed from a sustained increase to a transient spike when the average number of IP3 released is decreased below 50 molecules per nanocapsule. We also demonstrate the delivery of a 23 kDa O6-alkylguanine-DNA alkyltransferase (AGT) fusion protein into Ba/F3 cells to inhibit a key player BCR-ABL in the apoptotic pathway. We show that an average of ~8 molecules of the inhibitor is sufficient to induce apoptosis in the majority of Ba/F3 cells.
机译:本文介绍了一种方法,通过该方法,可将不渗透细胞的分子封装在染料敏化脂质纳米胶囊中,以通过内吞作用传递到细胞中。一旦进入细胞内部,分子就会从脂质纳米胶囊释放到细胞质中,而远红外线(645 nm)发出的激光会产生一个纳秒的脉冲。我们用CHO-M1细胞中的第二个信使IP3的细胞内释放证明了这种方法,并报告了当平均释放的IP3数量减少到每个纳米胶囊低于50个分子时,细胞的钙反应从持续增加变为瞬时峰值。我们还证明了23 kDa O6-烷基鸟嘌呤-DNA烷基转移酶(AGT)融合蛋白的交付到Ba / F3细胞中,以抑制凋亡途径中的关键球员BCR-ABL。我们发现平均约8个抑制剂分子足以诱导大多数Ba / F3细胞凋亡。

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