Even-Chen S, Barenholz Y
Laboratory of Membrane and Liposome Research, Department of Biochemistry, The Hebrew University - Hadassah Medical School, P.O. Box 12272, 91120, Jerusalem, Israel.
Biochim Biophys Acta. 2000 Dec 20;1509(1-2):176-88. doi: 10.1016/s0005-2736(00)00292-3.
Cationic liposomes and DNA interact electrostatically to form complexes called lipoplexes. The amounts of unbound (free) DNA in a mixture of cationic liposomes and DNA at different cationic lipid:DNA molar ratios can be used to describe DNA binding isotherms; these provide a measure of the binding efficiency of DNA to different cationic lipid formulations at various medium conditions. In order to quantify the ratio between the various forms of naked DNA and supercoiled, relaxed and single-stranded DNA, and the ratio between cationic lipid bound and unbound DNA of various forms we developed a simple, sensitive quantitative assay using agarose gel electrophoresis, followed by staining with the fluorescent cyanine DNA dyes SYBR Green I or SYBR Gold. This assay was compared with that based on the use of ethidium bromide (the most commonly used nucleic acid stain). Unlike ethidium bromide, SYBR Green I DNA sensitivity and concentration-dependent fluorescence intensity were identical for supercoiled and nicked-relaxed forms. DNA detection by SYBR Green I in solution is approximately 40-fold more sensitive than by ethidium bromide for double-stranded DNA and approximately 10-fold for single-stranded DNA, and in agarose gel it is 16-fold more sensitive for double-stranded DNA compared with ethidium bromide. SYBR Gold performs similarly to SYBR Green I. This study shows that: (a) there is no significant difference in DNA binding isotherms to the monocationic DOTAP (DOTAP/DOPE) liposomes and to the polycationic DOSPA (DOSPA/DOPE) liposomes, even when four DOSPA positive charges are involved in the electrostatic interaction with DNA; (b) the helper lipids affect DNA binding, as DOTAP/DOPE liposomes bind more DNA than DOTAP/cholesterol; (c) in the process of lipoplex formation, when the DNA is a mixture of two forms, supercoiled and nicked-relaxed (open circular), there is a preference for the binding to the cationic liposomes of plasmid DNA in the nicked-relaxed over the supercoiled form. This preference is much more pronounced when the cationic liposome formulation is based on the monocationic lipid DOTAP than on the polycationic lipid DOSPA. The preference of DOTAP formulations to bind to the relaxed DNA plasmid suggests that the binding of supercoiled DNA is weaker and easier to dissociate from the complex.
阳离子脂质体与DNA通过静电相互作用形成称为脂质体复合物的复合体。在不同阳离子脂质与DNA摩尔比下,阳离子脂质体和DNA混合物中未结合(游离)DNA的量可用于描述DNA结合等温线;这些等温线提供了在各种介质条件下DNA与不同阳离子脂质制剂结合效率的一种度量。为了量化各种形式的裸露DNA与超螺旋、松弛和单链DNA之间的比例,以及各种形式的阳离子脂质结合DNA与未结合DNA之间的比例,我们开发了一种简单、灵敏的定量测定方法,即使用琼脂糖凝胶电泳,然后用荧光花青DNA染料SYBR Green I或SYBR Gold染色。该测定方法与基于溴化乙锭(最常用的核酸染料)的方法进行了比较。与溴化乙锭不同,SYBR Green I对超螺旋和切口松弛形式的DNA敏感性和浓度依赖性荧光强度是相同的。在溶液中,SYBR Green I检测DNA的灵敏度比溴化乙锭检测双链DNA高约40倍,检测单链DNA高约10倍,在琼脂糖凝胶中,其检测双链DNA的灵敏度比溴化乙锭高16倍。SYBR Gold的表现与SYBR Green I类似。本研究表明:(a)即使在与DNA的静电相互作用中有四个DOSPA正电荷参与,单阳离子DOTAP(DOTAP/DOPE)脂质体和多阳离子DOSPA(DOSPA/DOPE)脂质体的DNA结合等温线也没有显著差异;(b)辅助脂质会影响DNA结合,因为DOTAP/DOPE脂质体比DOTAP/胆固醇结合更多的DNA;(c)在脂质体复合物形成过程中,当DNA是超螺旋和切口松弛(开环)两种形式的混合物时,切口松弛的质粒DNA比超螺旋形式更倾向于与阳离子脂质体结合。当阳离子脂质体制剂基于单阳离子脂质DOTAP时,这种倾向比基于多阳离子脂质DOSPA时更为明显。DOTAP制剂对松弛DNA质粒的优先结合表明,超螺旋DNA的结合较弱,更容易从复合物中解离。