Scarzello Marco, Chupin Vladimir, Wagenaar Anno, Stuart Marc C A, Engberts Jan B F N, Hulst Ron
Physical Organic Chemistry Unit, Stratingh Institute, University of Groningen, Nijenborgh 4, 9747 AG Groningen, The Netherlands.
Biophys J. 2005 Mar;88(3):2104-13. doi: 10.1529/biophysj.104.053983. Epub 2004 Dec 21.
Two double-tailed pyridinium cationic amphiphiles, differing only in the degree of unsaturation of the alkyl chains, have been selected for a detailed study of their aggregation behavior, under conditions employed for transfection experiments. The transfection efficiencies of the two molecules are remarkably different, especially when combined with 1,2-dioleoyl-sn-glycero-3-phosphoethanolamine (DOPE) as helper lipid. The phase behavior of the cationic amphiphile/DOPE mixtures have been studied using (31)P- and (2)H-NMR (on deuterated cationic amphiphiles) as main techniques, to monitor independently the behavior of the two components. In water, the lamellar organization is dominant for both the surfactants in their mixtures with the helper lipid. In HEPES saline buffer (HBS), the mixtures of the unsaturated surfactant form inverted phases and, in particular, stable H(II) phases for DOPE contents > or =30 mol %. By contrast, the saturated surfactant does not form homogeneously mixed inverted phases in mixtures with DOPE at room temperature. However, mixed inverted phases are observed for this system at higher temperatures and, after mixing has been achieved by heating, the metastable mixed phases remain present for several hours at 5 degrees C. At 35 degrees C the dominant phase is the cubic phase. The lipoplex composed of equimolar mixtures of the unsaturated surfactant with DOPE and plasmid DNA was found to be organized in highly curved bilayers.
选择了两种仅在烷基链不饱和度上有所不同的双尾吡啶鎓阳离子两亲物,在用于转染实验的条件下对其聚集行为进行详细研究。这两种分子的转染效率显著不同,尤其是当与1,2 - 二油酰 - sn - 甘油 - 3 - 磷酸乙醇胺(DOPE)作为辅助脂质结合时。已使用(31)P - 和(2)H - NMR(对氘代阳离子两亲物)作为主要技术研究了阳离子两亲物/DOPE混合物的相行为,以独立监测两种组分的行为。在水中,层状结构在它们与辅助脂质的混合物中对两种表面活性剂而言都是主要的。在HEPES盐缓冲液(HBS)中,不饱和表面活性剂的混合物形成反相,特别是当DOPE含量≥30摩尔%时形成稳定的H(II)相。相比之下,饱和表面活性剂在室温下与DOPE的混合物中不会形成均匀混合的反相。然而,在较高温度下观察到该体系的混合反相,并且在通过加热实现混合后,亚稳混合相在5℃下保持数小时。在35℃时,主要相是立方相。发现由不饱和表面活性剂与DOPE和质粒DNA的等摩尔混合物组成的脂质体以高度弯曲的双层形式组织。