Zuidam N J, Barenholz Y
Department of Biochemistry, The Hebrew University, Hadassah Medical School, Jerusalem, Israel.
Biochim Biophys Acta. 1997 Oct 23;1329(2):211-22. doi: 10.1016/s0005-2736(97)00110-7.
Cationic liposomes are used to deliver genes into cells in vitro and in vivo. The present study is aimed to characterize the electrostatic parameters of cationic, large unilamellar vesicles, 110 +/- 20 nm in size, composed of DOTAP/DOPE (mole ratio 1/1), DOTAP/DOPC (mole ratio 1/1), 100% DOTAP, DMRIE/DOPE 1/1, or DC-CHOL/DOPE (mole ratio 1/1). {
DOTAP, N-(1-(2,3-dioleoyloxy)propyl)-N,N,N-trimethylammonium chloride; DOPE, 1,2-dioleoyl-sn-glycero-3-phosphatidylethanolamine; DOPC, 1,2-dioleoyl-sn-glycero-3-phosphatidylcholine; DMRIE, 1,2-dimyristyloxypropyl-3-dimethyl-hydroxyethylammonium bromide; DC-CHOL, 3beta[N-(N',N'-dimethylaminoethane)carbamoyl]cholesterol}. The cationic liposomes had a large positive surface potential and a high pH at the liposomal surface in 20 mM Hepes buffer (pH 7.4) as monitored by the pH-sensitive fluorophore 4-heptadecyl-7-hydroxycoumarin. In contrast to DOTAP and DMRIE which were 100% charged, DC-CHOL in DC-CHOL/DOPE (1/1) liposomes was only about 50% charged in 20 mM Hepes buffer (pH 7.4). This might result in an easier dissociation of bilayers containing DC-CHOL from the plasmid DNA (which is necessary to enable transcription), in a decrease of the charge on the external surfaces of the liposomes or DNA-lipid complexes, and in an increase in release of the DNA-lipid complex into the cytosol from the endosomes. Other electrostatic characteristics found were that the primary amine group of DOPE in cationic liposomes dissociated at high (> 7.9) pHbulk and that a salt bridge was likely between the quaternary amine of DOTAP or DMRIE and the phosphate group of DOPE or DOPC, but not between the tertiary amine of DC-CHOL and the phosphate group of DOPE. The liposomes containing DOTAP were unstable upon dilution, probably due to the high critical aggregation concentration of DOTAP, 7 X 10(-5) M. This might also be a mechanism of the dissociation of bilayers containing DOTAP from the plasmid DNA.
阳离子脂质体用于在体外和体内将基因导入细胞。本研究旨在表征由DOTAP/DOPE(摩尔比1/1)、DOTAP/DOPC(摩尔比1/1)、100% DOTAP、DMRIE/DOPE 1/1或DC-CHOL/DOPE(摩尔比1/1)组成的大小为110±20 nm的阳离子大单层囊泡的静电参数。{
DOTAP,N-(1-(2,3-二油酰氧基)丙基)-N,N,N-三甲基氯化铵;DOPE,1,2-二油酰-sn-甘油-3-磷脂酰乙醇胺;DOPC,1,2-二油酰-sn-甘油-3-磷脂酰胆碱;DMRIE,1,2-二肉豆蔻酰氧基丙基-3-二甲基羟乙基溴化铵;DC-CHOL,3β[N-(N',N'-二甲基氨基乙烷)氨基甲酰]胆固醇}。通过pH敏感荧光团4-十七烷基-7-羟基香豆素监测发现,在20 mM Hepes缓冲液(pH 7.4)中,阳离子脂质体具有较大的正表面电位和脂质体表面的高pH值。与100%带电荷的DOTAP和DMRIE不同,DC-CHOL/DOPE(1/1)脂质体中的DC-CHOL在20 mM Hepes缓冲液(pH 7.4)中仅约50%带电荷。这可能导致含DC-CHOL的双层与质粒DNA更容易解离(这是实现转录所必需的),脂质体或DNA-脂质复合物外表面电荷减少,以及DNA-脂质复合物从内体释放到细胞质中的增加。发现的其他静电特征是,阳离子脂质体中DOPE的伯胺基团在高(>7.9)pH bulk下解离,并且DOTAP或DMRIE的季胺与DOPE或DOPC的磷酸基团之间可能形成盐桥,但DC-CHOL的叔胺与DOPE的磷酸基团之间不会形成盐桥。含DOTAP的脂质体在稀释时不稳定,这可能是由于DOTAP的高临界聚集浓度7×10(-5) M所致。这也可能是含DOTAP的双层与质粒DNA解离的一种机制。