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首页> 外文期刊>Analytical chemistry >Direct Cytosolic MicroRNA Detection Using Single-Layer Perfluorinated Tungsten Diselenide Nanoplatform
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Direct Cytosolic MicroRNA Detection Using Single-Layer Perfluorinated Tungsten Diselenide Nanoplatform

机译:使用单层全氟化钨纳米替纳纳薄纳米纳米甲基纳薄纳米甲醚直接细胞溶质微瘤检测

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摘要

Intracellular miRNA detection is vitally important for diagnosing severe diseases like cancer and for resolving the ensemble of gene products that orchestrate the living state of cells. Recent advances in the design, synthesis, and application of biocompatible nanomaterials as platforms for probing miRNAs have enabled widespread efforts to mobilize new compounds in biomedical research. Two-dimensional graphene-like nanomaterials exhibit desirable physical properties such as convenient quantum size and dynamic interface functionality. Because miRNAs regulate gene expression in the cytoplasm, it is imperative that nanomaterials targeting them are properly delivered. Unloading of nanomaterials into the cytosol using the cellular endocytic transport pathway is often hindered by an inability to cross the endosomal membrane. To address this challenge, we designed a strategy to deliver functionalized WSe2 nanosheets (FWNs) to the cytosol using perfluorinated surface functionalization. Perfluorinated compounds are both hydrophobic and lipophobic, exhibiting excellent phase-separation tendency in both polar and nonpolar environments. FWNs are similar to 120 nm in diameter, feature low toxicity, and exhibit excellent stability in serum. The fluorinated nanostructure of FWNs enabled efficient cytosolic delivery from the endomembrane system. The fidelity of this approach was confirmed through intracellular delivery of two DNA probes (ssDNA-21 and ssDNA-210), which resulted in specific labeling of cytosolic miRNA and demonstrated the utility of this system for direct cytosolic biosensing.
机译:细胞内miRNA检测对于诊断癌症等严重疾病并解决协调细胞生物状态的基因产品的集合来对诊断严重疾病至关重要。生物相容性纳米材料作为探测MiRNA平台的设计,合成和应用的最新进展使得努力在生物医学研究中动员新化合物。二维石墨烯样纳米材料表现出理想的物理性质,例如方便的量子尺寸和动态接口功能。因为miRNA调节细胞质中的基因表达,所以靶向它们的纳米材料必须适当地递送。使用细胞内吞传输途径卸载纳米材料进入细胞溶溶胶,通常阻碍通过不能通过内体膜来阻碍。为了解决这一挑战,我们设计了一种使用全氟化表面官能化将官能化WSE2纳米片(FWNS)递送至细胞溶质的策略。全氟化合物既是疏水性和脂恐生品,也都在极性和非极性环境中表现出优异的相分离趋势。 FWN与120nm的直径相似,具有低毒性,并且在血清中表现出优异的稳定性。 FWN的氟化纳米结构使能量来自端膜系统的有效细胞溶胶递送。通过两种DNA探针(SSDNA-21和SSDNA-210)的细胞内递送确认该方法的保真度,从而导致细胞溶质miRNA的特异性标记,并证明了该系统用于直接细胞溶质生物溶胶的实用性。

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  • 来源
    《Analytical chemistry》 |2018年第17期|共8页
  • 作者单位

    Washington State Univ Sch Mech &

    Mat Engn Pullman WA 99164 USA;

    Washington State Univ Sch Mech &

    Mat Engn Pullman WA 99164 USA;

    Washington State Univ Sch Biol Sci Pullman WA 99164 USA;

    Washington State Univ Sch Mech &

    Mat Engn Pullman WA 99164 USA;

    Zhengzhou Univ Coll Chem &

    Mol Engn Henan Joint Int Res Lab Green Construct Funct Mol Zhengzhou 450001 Henan Peoples R China;

    Washington State Univ Sch Mech &

    Mat Engn Pullman WA 99164 USA;

    Zhengzhou Univ Coll Chem &

    Mol Engn Henan Joint Int Res Lab Green Construct Funct Mol Zhengzhou 450001 Henan Peoples R China;

    Washington State Univ Sch Mech &

    Mat Engn Pullman WA 99164 USA;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 分析化学;
  • 关键词

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