Carlsson Nils, Sanandaji Nima, Voinova Marina, Akerman Björn
Department of Chemistry and Bioscience, Chalmers University of Technology, SE-41296 Göteborg, Sweden.
Langmuir. 2006 Apr 25;22(9):4408-14. doi: 10.1021/la052086l.
Porous hydrogels such as agarose are commonly used to analyze DNA and water-soluble proteins by electrophoresis. However, the hydrophilic environment of these gels is not suitable for separation of important amphiphilic molecules such as native membrane proteins. We show that an amphiphilic liquid crystal of the lipid monoolein and water can be used as a medium for electrophoresis of amphiphilic molecules. In fact, both membrane-bound fluorescent probes and water-soluble oligonucleotides can migrate through the same bicontinuous cubic crystal because both the lipid membrane and the aqueous phase are continuous. Both types of analytes exhibit a field-independent electrophoretic mobility, which suggests that the lipid crystal structure is not perturbed by their migration. Diffusion studies with four membrane probes indicate that membrane-bound analytes experience a friction in the cubic phase that increases with increasing size of the hydrophilic headgroup, while the size of the membrane-anchoring part has comparatively small effect on the retardation.
诸如琼脂糖之类的多孔水凝胶通常用于通过电泳分析DNA和水溶性蛋白质。然而,这些凝胶的亲水环境并不适合分离重要的两亲性分子,如天然膜蛋白。我们表明,脂质单油酸甘油酯和水的两亲性液晶可作为两亲性分子电泳的介质。事实上,膜结合荧光探针和水溶性寡核苷酸都可以通过相同的双连续立方晶体迁移,因为脂质膜和水相都是连续的。这两种分析物都表现出与电场无关的电泳迁移率,这表明脂质晶体结构不会因它们的迁移而受到干扰。对四种膜探针的扩散研究表明,膜结合分析物在立方相中受到的摩擦力会随着亲水头部基团尺寸的增加而增大,而膜锚定部分的尺寸对阻滞作用的影响相对较小。