Paterson L, Agate B, Comrie M, Ferguson R, Lake T, Morris J, Carruthers A, Brown C T, Sibbett W, Bryant P, Gunn-Moore F, Riches A, Dholakia Kishan
Opt Express. 2005 Jan 24;13(2):595-600. doi: 10.1364/opex.13.000595.
The introduction and subsequent expression of foreign DNA inside living mammalian cells (transfection) is achieved by photoporation with a violet diode laser. We direct a compact 405 nm laser diode source into an inverted optical microscope configuration and expose cells to 0.3 mW for 40 ms. The localized optical power density of 1200 MW/m2 is six orders of magnitude lower than that used in femtosecond photoporation (104 TW/m2). The beam perforates the cell plasma membrane to allow uptake of plasmid DNA containing an antibiotic resistant gene as well as the green fluorescent protein (GFP) gene. Successfully transfected cells then expand into clonal groups which are used to create stable cell lines. The use of the violet diode laser offers a new and simple poration technique compatible with standard microscopes and is the simplest method of laser-assisted cell poration reported to date.
通过使用紫光二极管激光进行光穿孔,可实现外源DNA在活的哺乳动物细胞内的导入及后续表达(转染)。我们将一个紧凑的405 nm激光二极管光源导入倒置光学显微镜配置中,并将细胞暴露于0.3 mW的光线下40毫秒。约1200 MW/m²的局部光功率密度比飞秒光穿孔中使用的光功率密度(约10⁴ TW/m²)低六个数量级。光束穿透细胞质膜,使含有抗生素抗性基因以及绿色荧光蛋白(GFP)基因的质粒DNA得以摄取。成功转染的细胞随后扩展为克隆群体,用于创建稳定的细胞系。紫光二极管激光的使用提供了一种与标准显微镜兼容的全新且简单的穿孔技术,是迄今为止报道的最简单的激光辅助细胞穿孔方法。