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二元DMTAP/DOTAP阳离子脂质体与质粒DNA相互作用的量热研究

Calorimetric study of the interaction of binary DMTAP/DOTAP cationic liposomes with plasmid DNA.

作者信息

Giatrellis Sarantis, Nikolopoulos George, Sideratou Zili, Nounesis George

机构信息

Biomolecular Physics Laboratory, IRRP, National Centre for Scientific Research Demokritos, Aghia Paraskevi, Greece.

出版信息

J Liposome Res. 2009;19(3):220-30. doi: 10.1080/08982100902746596.

Abstract

Cationic liposomes have been suggested as possible agents for nonviral gene transfer. The interaction of plasmid DNA (pDNA) with dispersions of stable unilamellar cationic liposomes based on the binary lipid system 1,2-dimyristoyl-3-trimethyl-ammonium-propane (DMTAP):1,2-dioleoyl-3-trimethyl-ammonium-propane (DOTAP) has been studied by using isothermal titration calorimetry (ITC), high-precision differential scanning calorimetry (DSC), dynamic light scattering (DLS), and circular dichroism (CD). Systematic calorimetric and DLS exploration of the DMTAP:DOTAP binary system reveals that single-bilayer liposomes are stable at the 4:1 molar ratio, exhibiting the main lipid-phase transition temperature at approximately 25.3 degrees C, and a total enthalpy change deltaH = 8.5 +/- 0.4 kcal/mol. The interaction of pDNA with unilamellar DMTAP:DOTAP vesicles was investigated by ITC experiments, which clearly distinguished endothermic binding between the phosphate and the ammonium groups from exothermic processes, driven by slow kinetics, corresponding to interliposomal, DNA-triggered aggregation that leads to the formation of large multilamellar liposome/pDNA assemblies. Lipid-added-to-pDNA and pDNA-added-to-lipid experiments have been carried out in order to systematically explore the interaction mechanisms. Complex ITC profiles are revealed, which may be linked to packing rearrangements of the pDNA molecules bound at the outer liposomal surface, possibly due to binding to more than one liposome or due to p-DNA-enhanced heterogeneity in the local lipid concentration. DNA-mediated aggregation effects are detected at high [ammonium]/[phosphate] molar ratios in the case of lipid-added-to-pDNA interactions and at relatively low [phosphate]/[ammonium] molar ratios in the case of pDNA-added-to-lipid.

摘要

阳离子脂质体已被认为是用于非病毒基因转移的可能媒介。基于二元脂质体系1,2-二肉豆蔻酰-3-三甲基铵丙烷(DMTAP):1,2-二油酰-3-三甲基铵丙烷(DOTAP)的稳定单层阳离子脂质体分散体与质粒DNA(pDNA)的相互作用已通过等温滴定量热法(ITC)、高精度差示扫描量热法(DSC)、动态光散射(DLS)和圆二色性(CD)进行了研究。对DMTAP:DOTAP二元体系进行的系统量热和DLS研究表明,单层脂质体在4:1摩尔比下是稳定的,其主要脂质相变温度约为25.3℃,总焓变ΔH = 8.5±0.4千卡/摩尔。通过ITC实验研究了pDNA与单层DMTAP:DOTAP囊泡的相互作用,该实验清楚地将磷酸盐和铵基团之间的吸热结合与由缓慢动力学驱动的放热过程区分开来,后者对应于脂质体间由DNA触发的聚集,导致形成大型多层脂质体/pDNA组装体。为了系统地探索相互作用机制,进行了脂质添加到pDNA和pDNA添加到脂质的实验。揭示了复杂的ITC曲线,这可能与结合在脂质体表面外层的pDNA分子的堆积重排有关,可能是由于与不止一个脂质体结合或由于局部脂质浓度中p-DNA增强的异质性。在脂质添加到pDNA相互作用中,在高[铵]/[磷酸盐]摩尔比下检测到DNA介导的聚集效应;在pDNA添加到脂质的情况下,在相对低的[磷酸盐]/[铵]摩尔比下检测到该效应。

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