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Lipid-Nucleic Acid Supramolecular Complexes: Lipoplex Structure and the Kinetics of Formation

机译:脂质-核酸超分子复合物:脂质复合物结构和形成动力学

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The need for synthetic gene therapy or gene silencing vehicles that can insert therapeutic nucleic acids (DNA or siRNA) into cells (so-called transfection) has focused interest on lipid-nucleic acid assemblies (lipoplexes). This paper reviews the kinetics pathways leading to lipoplex formation and structure. The process is qualitatively comparable to those of cluster nucleation and growth and to the adsorption of polyelectrolytes on colloidal particles: Initially is a rapid stage where the nucleic acid binds onto the surface of the cationic lipid aggregate (adsorption, or nucleation). This is followed by an intermediate step where the lipiducleic acid complexes flocculate to form larger structures (growth). The last and final step involves internal rearrangement, where the overall global structure remains constant while local adjustment of the nucleic acid/lipid organization takes place until the equilibrium lipoplex characteristics are obtained. This step can require unusually long time scales of order hours or longer. Understanding the kinetics of lipoplex formation is not only of fundamental interest as a multi-component, multi-length scale and multi-time scale process, but also has significant implications for the utilization of lipoplexes as carriers for gene delivery and gene silencing agents.
机译:可以将治疗性核酸(DNA或siRNA)插入细胞(所谓的转染)的合成基因治疗或基因沉默载体的需求,引起了人们对脂质-核酸组装体(脂质复合物)的关注。本文综述了导致脂质体形成和结构的动力学途径。该过程在质量上与簇状成核和生长以及聚电解质在胶体颗粒上的吸附具有可比性:最初是一个快速阶段,核酸与阳离子脂质聚集体的表面结合(吸附或成核)。随后是中间步骤,其中脂质/核酸复合物絮凝形成更大的结构(生长)。最后也是最后一步涉及内部重排,其中总体整体结构保持恒定,同时对核酸/脂质组织进行局部调节,直到获得平衡脂复合物特性。此步骤可能需要异常长时间的订单小时数或更长时间。理解脂质复合物形成的动力学不仅是作为多组分,多长度规模和多时间规模过程的基本兴趣,而且对于利用脂质复合物作为基因递送和基因沉默剂的载体也具有重要意义。

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