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用光寻址纳米胶囊实现生物活性分子的细胞内递送。

Intracellular delivery of bioactive molecules using light-addressable nanocapsules.

机构信息

Chemistry Department, University of Washington, Seattle, Washington, USA.

出版信息

ACS Nano. 2010 Dec 28;4(12):7603-11. doi: 10.1021/nn102345f. Epub 2010 Nov 30.

Abstract

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 IP(3) 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 IP(3) released is decreased below 50 molecules per nanocapsule. We also demonstrate the delivery of a 23 kDa O(6)-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.

摘要

本文描述了一种将不能穿透细胞的分子封装在染料敏化脂质纳米胶囊中的方法,以便通过细胞内吞作用将其递送至细胞内。一旦进入细胞,分子就会从脂质纳米胶囊中释放到细胞质中,只需用远红光(645nm)中的激光发出一个纳秒脉冲即可。我们用 CHO-M1 细胞中第二信使 IP(3)的细胞内释放证明了这种方法,并报告了当每个纳米胶囊释放的 IP(3)分子数平均低于 50 个时,细胞内的钙反应从持续增加变为瞬时尖峰。我们还演示了将 23kDa O(6)-烷基鸟嘌呤-DNA 烷基转移酶(AGT)融合蛋白递送至 Ba/F3 细胞中,以抑制凋亡途径中的关键蛋白 BCR-ABL。我们表明,平均约 8 个抑制剂分子足以诱导大多数 Ba/F3 细胞凋亡。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2619/3075813/584bf06511ff/nihms255585f1.jpg

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