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Recognition and transmembrane delivery of bioconjugated Fe2O3@Au nanoparticles with living cells

机译:识别和跨膜传递bioconjugated Fe2O3@Au纳米粒子与生活细胞

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摘要

Here, we describe the synthesis of peptide- and/or protein-functionalized Fe2O3 core-Au shell (Fe2O3@Au) nanoparticles for imaging and targeting of living cells. When functionalized with the transmembrane peptide RRRRRRRR (R8), the Fe2O3@Au nanoparticles (R8-Fe2O3@Au) are able to serve as cellular trafficking agents with excellent biocompatibility. The internalization mechanism and delivery efficiency of the R8-Fe2O3@Au nanoparticles have been characterized with dark-field microscopy and fluorescence confocal scanning laser microcopy. Experimental result suggests that the R8-Fe2O3@Au nanoparticles are internalized initially by binding with the membrane-associated proteoglycans on cell surfaces, especially heparan sulfate proteoglycans (HSPGs), following an energy-dependent endocytosis process to enter into living cells. After conjugation with the epidermal growth factor receptor antibody (anti-EGFR), these nanoparticles can also be used for the recognition of cell membrane antigens to specifically label tumor cells.
机译:在这里,我们描述的合成肽-和/或protein-functionalized Fe2O3 core-Au壳(Fe2O3@Au)成像和纳米颗粒目标的活细胞。跨膜肽RRRRRRRR (R8)Fe2O3@Au纳米颗粒(R8-Fe2O3@Au)都可以作为细胞贩运代理良好的生物相容性。机制和交付的效率R8-Fe2O3@Au纳米粒子的特点暗视野显微镜和荧光共焦扫描激光缩微复制。结果表明,R8-Fe2O3@Au纳米粒子是最初的内化绑定与膜相关的对细胞表面蛋白聚糖,尤其是硫酸乙酰肝素蛋白聚糖(HSPGs)进入一个能量依赖性内吞作用过程到活细胞。表皮生长因子受体抗体(anti-EGFR),这些纳米粒子也可以使用细胞膜抗原的识别具体标签肿瘤细胞。

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