Pupo Elder
Department of Vaccinology, National Institute for Public Health and the Environment (RIVM), Bilthoven, The Netherlands.
Methods Mol Biol. 2011;739:101-12. doi: 10.1007/978-1-61779-102-4_9.
Polyacrylamide slab gel electrophoresis in the presence of sodium dodecyl sulfate or sodium deoxycholate (SDS- or DOC-slab-PAGE) is a powerful technique for the separation of smooth(S)-type bacterial lipopolysaccharides (LPS). In order to recover the individual LPS species from the polyacrylamide gel for subsequent analyses, a sensitive, nondestructive reverse staining of slab-PAGE-separated LPS has been developed. The individual reverse-stained LPS bands can be rapidly and efficiently recovered into an aqueous 5% triethylamine solution when they are extruded to produce fine gel microparticles. Based on these principles, an isolation methodology that combines preparative slab-PAGE, reverse staining, extrusion, and passive elution can be used to isolate, to electrophoretic homogeneity, micrograms to hundreds of micrograms of individual LPS species successfully from smooth-type LPS mixtures.
在十二烷基硫酸钠或脱氧胆酸钠存在下进行的聚丙烯酰胺平板凝胶电泳(SDS - 或DOC - 平板PAGE)是分离光滑型(S)细菌脂多糖(LPS)的强大技术。为了从聚丙烯酰胺凝胶中回收单个LPS种类以便后续分析,已开发出一种对平板PAGE分离的LPS进行灵敏、非破坏性的反向染色方法。当将单个反向染色的LPS条带挤出以产生细小的凝胶微粒时,它们可以快速有效地回收到5%三乙胺水溶液中。基于这些原理,一种结合制备型平板PAGE、反向染色、挤出和被动洗脱的分离方法可用于从光滑型LPS混合物中成功分离出微克至数百微克电泳均一的单个LPS种类。