首页> 美国卫生研究院文献>other >Detection of extracellular RNAs in cancer and viral infection via tethered cationic lipoplex nanoparticles containing molecular beacons
【2h】

Detection of extracellular RNAs in cancer and viral infection via tethered cationic lipoplex nanoparticles containing molecular beacons

机译:通过包含分子信标的阳离子阳离子脂复合物纳米颗粒检测癌症和病毒感染中的细胞外RNA

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Non-invasive early detection methods have the potential to reduce mortality rates of both cancer and infectious diseases. Here, we present a novel assay by which tethered cationic lipoplex nanoparticles containing molecular beacons (MBs) can capture cancer cell-derived exosomes or viruses, and identify encapsulated RNAs in a single step. A series of ultracentrifugation and Exoquick™ isolation kit were first used to isolate exosomes from the cell culture medium and human serum respectively. Cationic lipoplex nanoparticles linked onto the surface of a thin glass plate capture negatively charged viruses or cell-secreted exosomes by electrostatic interactions to form larger nanoscale complexes. Lipoplex/virus or lipoplex/exosome fusion leads to the mixing of viral/exosomal RNAs and MBs within the lipoplexes. After the target RNAs specially bind to the MBs, exosomes enriched in target RNAs are readily identified by the fluorescence signals of MBs. The in situ detection of target extracellular RNAs without diluting the samples leads to high detection sensitivity not achievable by existing methods, e.g. qRT-PCR. Here we demonstrate this concept using lentivirus and serum from lung cancer patients.
机译:非侵入性早期检测方法具有降低癌症和传染病死亡率的潜力。在这里,我们提出了一种新颖的测定法,通过该测定法,包含分子信标(MBs)的束缚阳离子脂质体纳米颗粒可以捕获癌细胞衍生的外来体或病毒,并在一个步骤中鉴定出被包封的RNA。首先使用一系列的超速离心和Exoquick™分离试剂盒分别从细胞培养基和人血清中分离出外泌体。连接到薄玻璃板表面的阳离子脂复合物纳米颗粒通过静电相互作用捕获带负电荷的病毒或细胞分泌的外来体,从而形成更大的纳米级复合物。脂质复合物/病毒或脂质复合物/外来体融合导致脂质复合物中病毒/外泌体RNA和MB的混合。在靶RNA与MBs特异性结合后,通过MBs的荧光信号可以容易地鉴定出富含靶RNA的外泌体。在不稀释样品的情况下原位检测靶细胞外RNA会导致现有检测方法无法实现的高检测灵敏度。定量RT-PCR。在这里,我们使用慢病毒和肺癌患者血清证明了这一概念。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号