Cotten M, Baker A, Birnstiel M L, Zatloukal K, Wagner E
Institute for Molecular Pathology, Vienna, Austria.
Curr Protoc Hum Genet. 2001 May;Chapter 12:Unit 12.3. doi: 10.1002/0471142905.hg1203s11.
This unit describes preparation of adenovirus-polylysine-DNA complexes, which is useful for transfection of DNA into a variety of cell types. A DNA complex is prepared with biotinylated adenovirus and streptavidin-polylysine, coupled to transferrin, and used to transfect cells. Several support protocols describe methods for adenovirus growth and purification, biotinylation, inactivation with psoralen, and quantitation of the adenovirus particles. Additional support protocols describes preparation of streptavidin-polylysine and transferrin-polylysine, necessary for the basic procedure. The DNA used for transfection must be free of lipopolysaccharide (LPS), and two methods for removing LPS are described. A more direct polylysine-virus linkage that is simple and requires no exotic reagents can be used for transfection. This protocol requires polylysine-modified adenovirus, prepared as described. An alternate protocol describes transfecting cells with free virus and DNA condensed with a polycation.
本单元描述了腺病毒-聚赖氨酸-DNA复合物的制备方法,该复合物可用于将DNA转染到多种细胞类型中。用生物素化的腺病毒和与转铁蛋白偶联的链霉亲和素-聚赖氨酸制备DNA复合物,并用于转染细胞。几个辅助方案描述了腺病毒生长和纯化、生物素化、补骨脂素灭活以及腺病毒颗粒定量的方法。其他辅助方案描述了基础操作所需的链霉亲和素-聚赖氨酸和转铁蛋白-聚赖氨酸的制备方法。用于转染的DNA必须不含脂多糖(LPS),并描述了两种去除LPS的方法。一种更直接的聚赖氨酸-病毒连接方法简单,无需特殊试剂,可用于转染。本方案需要按照所述方法制备的聚赖氨酸修饰腺病毒。另一种方案描述了用游离病毒和与聚阳离子凝聚的DNA转染细胞。