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Viruslike Element-Tagged Nanoparticle Inductively Coupled Plasma Mass Spectrometry Signal Multiplier: Membrane Biomarker Mediated Cell Counting

机译:病毒状元素标记的纳米粒子电感耦合等离子体质谱信号倍增器:膜生物标志物介导的细胞计数

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摘要

Although rare cancerous cells are considered as more objective indications for a precise early diagnosis of cancers, accurate counting of them still is a spirited challenge. We reported a signal multiplication strategy by constructing element tagged viruslike nanoparticles (VLNPs) with a precise number of atoms for a membrane biomarker mediated higher sensitive cell counting using inductively coupled plasma mass spectrometry (ICPMS). Typical bacteriophage MS2 was exemplified to demonstrate the effectiveness of the element-tagged VLNPs as signal multipliers. Dibenzylcyclooctynepoly(ethylene glycol)-folate (DBCO-PEG-FA) and DOTA-Eu complex tag modified (FA-PEG)(69)-MS2-(DOTA-Eu)(965) targeted the folate receptor (FR) on KB cells as low as subzeptomole FRs could be quantified by Eu-153-species unspecific isotope dilution ICPMS, allowing us to be able to count at least 5 KB cells. While more than 2197 KB cells were needed to give a significant ICPMS signal using FA-PEG-DOTA-Eu, demonstrating more than 2 orders of magnitude signal multiplication and resulting in total 4.0 X 10(8) times signal amplification relative to one KB cell. We believe that such a signal multiplication strategy can be expanded to quantify and count other membrane biomarkers and their host cells using various VLNPs modified with different kinds and precise numbers of elements and guiding groups. In this way, prescribed multiples of signal amplification can be realized for a more accurate ICPMS-based quantitative bioanalysis because targeted molecules/cells in a complicated biological system might exist in orders of magnitude wide concentration range.
机译:虽然罕见的癌细胞被认为是精确的早期诊断癌症的更具目的的指示,但准确计数它们仍然是一种充满激烈的挑战。我们通过将元素标记的病毒纳米颗粒(VLNP)构建具有精确数量的原子来报告信号倍增策略,用于使用电感耦合等离子体质谱(ICPM)介导的膜生物标志物介导的更高的敏感细胞计数。典型的噬菌体MS2被例示为展示元素标记的VLNP的有效性作为信号乘法器。二苄基环唑二苯(二苄基环) - 丁酸酯(DBCO-PEG-FA)和DOTA-EU复合物标签改性(FA-PEG)(69)-MS2-(DOTA-EU)(965)靶向KB细胞上的叶酸受体(FR)低至SubβFRS可以通过Eu-153种未特异性同位素稀释ICPMS量化,使我们能够计数至少5kb的细胞。虽然需要超过2197kB的细胞来使用FA-PEG-DOTA-欧盟提供重要的ICPMS信号,但是呈现出超过2个幅度信号倍增的2个以上,导致相对于一个KB单元格总量为4.0×10(8)次信号放大。我们认为,可以扩展这种信号倍增策略以使用以不同种类和精确数量的元素和指导组改性的各种VLNP来量化和计算其他膜生物标志物及其宿主细胞。以这种方式,可以实现规定的信号放大倍数,以实现更准确的基于ICPMS的定量生物分析,因为复杂生物系统中的靶分子/细胞可能以较大的宽度浓度范围存在。

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  • 来源
    《Analytical chemistry》 |2019年第8期|共5页
  • 作者单位

    Xiamen Univ Coll Chem &

    Chem Engn Dept Chem Xiamen 361005 Peoples R China;

    Xiamen Univ Coll Chem &

    Chem Engn Dept Chem Xiamen 361005 Peoples R China;

    Xiamen Univ Coll Chem &

    Chem Engn Dept Chem Xiamen 361005 Peoples R China;

    Xiamen Univ Coll Chem &

    Chem Engn Dept Chem Xiamen 361005 Peoples R China;

    Xiamen Univ Coll Chem &

    Chem Engn Dept Chem Xiamen 361005 Peoples R China;

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