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首页> 外文期刊>Scientific reports. >Selective Capture and Purification of MicroRNAs and Intracellular Proteins through Antisense-vectorized Magnetic Nanobeads
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Selective Capture and Purification of MicroRNAs and Intracellular Proteins through Antisense-vectorized Magnetic Nanobeads

机译:通过反义向量化的磁性纳米珠的选择性捕获和纯化的microRNA和细胞内蛋白。

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摘要

MicroRNAs (miRNAs) are small non-coding nucleotides playing a crucial role in posttranscriptional expression and regulation of target genes in nearly all kinds of cells. In this study, we demonstrate a reliable and efficient capture and purification of miRNAs and intracellular proteins using magnetic nanoparticles functionalized with antisense oligonucleotides. For this purpose, a tumor suppressor miRNA (miR-198), deregulated in several human cancer types, was chosen as the model oligonucleotide. Magnetite nanoparticles carrying the complementary sequence of miR-198 (miR-198 antisense) on their surface were delivered into cells and subsequently used for the extracellular transport of miRNA and proteins. The successful capture of miR-198 was demonstrated by isolating RNA from magnetic nanoparticles followed by real-time PCR quantification. Our experimental data showed that antisense-coated particles captured 5-fold higher amounts of miR-198 when compared to the control nanoparticles. Moreover, several proteins that could play a significant role in miR-198 biogenesis were found attached to miR-198 conjugated nanoparticles and analyzed by mass spectrometry. Our findings demonstrate that a purpose-driven vectorization of magnetic nanobeads with target-specific recognition ligands is highly efficient in selectively transporting miRNA and disease-relevant proteins out of cells and could become a reliable and useful tool for future diagnostic, therapeutic and analytical applications.
机译:MicroRNA(miRNA)是小的非编码核苷酸,在几乎所有类型的细胞中,在转录后表达和靶基因的调控中起着至关重要的作用。在这项研究中,我们证明了使用反义寡核苷酸功能化的磁性纳米粒子可靠,有效地捕获和纯化miRNA和细胞内蛋白质。为此,选择了在几种人类癌症类型中均失控的抑癌miRNA(miR-198)作为模型寡核苷酸。在其表面上携带miR-198互补序列(miR-198反义)的磁铁矿纳米颗粒被递送到细胞中,随后用于miRNA和蛋白质的细胞外运输。通过从磁性纳米颗粒中分离RNA,然后进行实时PCR定量,证明了miR-198的成功捕获。我们的实验数据表明,与对照纳米颗粒相比,反义涂层颗粒捕获的miR-198量高5倍。此外,发现可能在miR-198生物发生中起重要作用的几种蛋白质与miR-198共轭纳米颗粒相连,并通过质谱分析。我们的发现表明,具有靶标特异性识别配体的磁性纳米珠的目标驱动载体化在选择性地将miRNA和与疾病相关的蛋白质转运出细胞方面非常有效,并且可能成为未来诊断,治疗和分析应用的可靠和有用的工具。

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