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Engineering functional nanoparticles for delivery in cells

机译:用于在细胞中递送的工程功能纳米粒子

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The ability of DNA functionalised gold nanoparticles (AuNPs) to detect specific targets in vitro and in vivo has led totheir development as suitable tools for sensing applications. However, endosomal entrapment is a common barrier invarious nanoparticle delivery approaches. In this work, we present a new design strategy with the aim to enhanceendosomal escape of DNA-coated AuNPs via the incorporation of a peptide that has been found to promote effectiveescape within cells. AuNPs are firstly modified with thiol terminated DNA strands followed by further surfacefunctionalisation with cysteine terminated peptides. We show that optimized loading of peptides following DNAnanoparticle functionalisation of nanoparticles is feasible. DNA-peptide-coated AuNP hybrids show similar stabilitytowards degradation by endocellular enzymes and similar specificity towards the detection of specific mRNA targets.
机译:DNA官能化金纳米颗粒(AUNP)在体外检测特异性靶标的能力导致他们的开发作为感应应用的合适工具。然而,内体夹紧是一种常见的障碍各种纳米粒子递送方法。在这项工作中,我们提出了一种新的设计策略,旨在增强通过掺入已发现促进有效的肽的DNA涂覆的AUNPS的内体逸出在细胞内逃脱。首先用硫醇封端的DNA链改性剖腹产,然后进一步改变用半胱氨酸封端肽的功能化。我们表明DNA以下优化的肽负载纳米颗粒的纳米粒子官能化是可行的。 DNA-肽涂层的AUNP杂交种显示出类似的稳定性通过内皮细胞酶降解和对检测特异性mRNA靶的特异性。

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