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High-Affinity PEGylated Polyacridine Peptide Polyplexes Mediate Potent In Vivo Gene Expression

机译:高亲和力聚乙二醇化聚丙烯肽络合在体内基因表达中介导有效

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摘要

PEGylated polyacridine peptides bind to plasmid DNA with high affinity to form unique polyplexes that possess a long circulatory half-life and are hydrodynamically (HD)-stimulated to produce efficient gene expression in the liver of mice. We previously demonstrated that (Acr-Lys)6-Cys-PEG5kDa stabilizes a 1 μg pGL3 dose for up to 1 hr in the circulation, resulting in HD-stimulated (saline only) gene expression in the liver, equivalent in magnitude to direct-HD dosing of 1 μg of pGL3 (Fernandez C.A. et al. Gene Therapy 2011). In the present study we report that increasing the spacing of Acr with either 4 or 5 Lys residues, dramatically increases the stability of PEGylated polyacridine peptide polyplexes in the circulation allowing maximal HD-stimulated expression for up to 5 hrs post-DNA administration. Co-administration of a decoy dose of 9 μg of non-expressing DNA polyplex with 1 μg of pGL3 polyplex further extended the HD-stimulated expression to 9 hrs. This structure-activity relationship study defines the PEGylated polyacridine peptide requirements for maintaining fully transfection competent plasmid DNA in the circulation for 5 hrs and provides an understanding as to why polyplexes or lipoplexes prepared with PEI, chitosan or Lipofectamine are inactive within 5 min following i.v. dosing.
机译:聚乙二醇化的聚丙烯肽与具有高亲和力的质粒DNA结合,形成具有长循环半衰期的独特的多种,并且是流体动力学(HD) - 在小鼠肝脏中产生有效的基因表达。我们之前证明(ACR-LYS)6-CYS-PEG5KDA稳定1μgPGL3剂量在循环中最多1小时,导致肝脏中的HD刺激(仅盐水)基因表达,其幅度相当于直接 - HD剂量为1μgPGL3(Fernandez Ca等人。基因治疗2011)。在本研究中,我们报告说,增加了ACR与4或5个Lys残基的间隔,显着提高了循环中的聚乙二醇化聚丙烯肽肽中的稳定性,允许最大的HD刺激的表达至多5小时的DNA给药。共同施用9μg非表达DNA多重与1μgPGL3多分发的非表达DNA多重进一步将HD刺激的表达延伸至9小时。该结构 - 活性关系研究定义了用于在循环中保持完全转染的态性质粒DNA的聚乙二醇化聚丙烯肽要求5小时,并提供了用PEI,壳聚糖或Lipofectamine制备的多重或脂质物在I.v后5分钟内无活性的良好分布或脂蛋体。给药。

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