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Nanoparticle-based bio-bar codes for the ultrasensitive detection of proteins

机译:基于纳米粒子的生物条形码,用于蛋白质的超灵敏检测

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摘要

An ultrasensitive method for detecting protein analytes has been developed. The system relies on magnetic microparticle probes with antibodies that specifically bind a target of interest [prostate-specific antigen (PSA) in this case] and nanoparticle probes that are encoded with DNA that is unique to the protein target of interest and antibodies that can sandwich the target captured by the microparticle probes. Magnetic separation of the complexed probes and target followed by dehybridization of the oligonucleotides on the nanoparticle probe surface allows the determination of the presence of the target protein by identifying the oligonucleotide sequence released from the nanoparticle probe. Because the nanoparticle probe carries with it a large number of oligonucleotides per protein binding event, there is substantial amplification and PSA can be detected at 30 attomolar concentration. Alternatively, a polymerase chain reaction on the oligonucleotide bar codes can boost the sensitivity to 3 attomolar. Comparable clinically accepted conventional assays for detecting the same target have sensitivity limits of approx 3 picomdar, six orders of magnitude less sensitive than what is observed with this method.
机译:已经开发了用于检测蛋白质分析物的超灵敏方法。该系统依赖于具有特异性结合目标靶标[在此情况下为前列腺特异性抗原(PSA)]的抗体的磁性微粒探针,以及由目标蛋白质靶标独有的DNA编码的纳米颗粒探针以及可以夹在中间的抗体微粒探针捕获的目标。磁性分离复合探针和靶标,然后对纳米颗粒探针表面上的寡核苷酸进行去杂化,可以通过鉴定从纳米颗粒探针释放的寡核苷酸序列来确定靶蛋白的存在。因为纳米粒子探针在每个蛋白质结合事件中都带有大量寡核苷酸,所以存在大量扩增,并且可以在30 atmol的摩尔浓度下检测到PSA。或者,在寡核苷酸条形码上的聚合酶链反应可将灵敏度提高至3 atmol。用于检测相同靶标的可比较的临床公认常规测定法的灵敏度极限约为3皮康,比使用此方法观察到的灵敏度低六个数量级。

著录项

  • 来源
    《Science》 |2003年第5641期|p.1884-1886|共3页
  • 作者单位

    Department of Chemistry and Institute for Nanotech-nology, Northwestern University, 2145 Sheridan Road, Evanston, IL 60201, USA;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 自然科学总论;
  • 关键词

  • 入库时间 2022-08-18 02:57:15

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