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Nanoparticle for delivery of antisense γPNA oligomers targeting CCR5

机译:用于递送靶向CCR5的反义γPNA低聚物的纳米颗粒

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摘要

The development of a new class of peptide nucleic acids (PNAs), i.e., gamma PNAs (γPNAs), creates the need for a general and effective method for its delivery into cells for regulating gene expression in mammalian cells. Here we report the antisense activity of a recently developed hydrophilic and biocompatible diethylene glycol (miniPEG)-based gamma peptide nucleic acid called MPγPNAs via its delivery by poly(lactide-co-glycolide) (PLGA)-based nanoparticle system. We show that MPγPNA oligomers designed to bind to the selective region of Chemokine Receptor 5 (CCR5) transcript, induce potent and sequence-specific antisense effects as compared with regular PNA oligomers. In addition, PLGA nanoparticle delivery of MPγPNAs is not toxic to the cells. The findings reported in this study provide a combination of γPNA technology and PLGA-based nanoparticle delivery method for regulating gene expression in live cells via the antisense mechanism.
机译:新型肽核酸(PNA),即γPNA(γPNAs)的发展,产生了对将其递送到细胞中以调节哺乳动物细胞中基因表达的通用有效方法的需求。在这里,我们报道了最近开发的基于亲水性和生物相容性的基于二甘醇(miniPEG)的亲水性γ肽核酸( MP γPNAs)的反义活性,该核酸通过聚丙交酯-乙交酯(PLGA)-基于纳米粒子的系统。我们显示, MP γPNA寡聚体旨在与趋化因子受体5(CCR5)转录物的选择性区域结合,与常规PNA寡聚体相比,诱导了有效的和序列特异性反义作用。此外, MP γPNAs的PLGA纳米颗粒递送对细胞无毒。这项研究报告的发现提供了γPNA技术和基于PLGA的纳米颗粒递送方法的组合,可通过反义机制调节活细胞中的基因表达。

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