School of Environment and Science , Griffith University Nathan Campus , Nathan , Queensland 4111 , Australia.
Queensland Micro and Nanotechnology Centre (QMNC) , Griffith University Nathan Campus , Nathan , Queensland 4111 , Australia.
Anal Chem. 2019 Mar 19;91(6):3827-3834. doi: 10.1021/acs.analchem.8b03619. Epub 2019 Feb 25.
Most of the current exosome-analysis strategies are time-consuming and largely dependent on commercial extraction kit-based preisolation step, which requires extensive sample manipulations, costly isolation kits, reagents, tedious procedures, and sophisticated equipment and is prone to bias/artifacts. Herein we introduce a simple method for direct isolation and subsequent detection of a specific population of exosomes using an engineered superparamagnetic material with multifunctional properties, namely, gold-loaded ferric oxide nanocubes (Au-NPFeONC). In this method, the Au-NPFeONC were initially functionalized with a generic tetraspanin (exosomes-associated) antibody (i.e., CD63) and dispersed in sample fluids where they work as "dispersible nanocarriers" to capture the bulk population of exosomes. After magnetic collection and purification, Au-NPFeONC-bound exosomes were transferred to the tissue-specific, antibody-modified, screen-printed electrode. As a proof of principle, we used a specific placental marker, placenta alkaline phosphatase (PLAP), to detect exosomes secreted from placental cells. The peroxidase-like activity of Au-NPFeONC was then used to accomplish an enzyme-linked immunosorbent assay (ELISA)-based sensing protocol for naked-eye observation along with UV-visible and electrochemical detection of PLAP-specific exosomes present in placental cell-conditioned media. We demonstrated excellent agreement in analytical performance for the detection of placental cell-derived exosomes (i.e., linear dynamic range, 10-10 exosomes/mL; limit of detection, 10 exosomes/mL; relative standard deviation (%RSD) of <5.5% for n = 3) using with and without commercial "total exosome isolation kit"-based preisolation step. We envisage that this highly sensitive, rapid, and inexpensive assay could be useful in quantifying specific populations of exosomes for various clinical applications, focusing on pregnancy complications.
目前大多数的外泌体分析策略都很耗时,并且在很大程度上依赖于基于商业提取试剂盒的预分离步骤,该步骤需要广泛的样本操作、昂贵的分离试剂盒、试剂、繁琐的程序以及复杂的设备,并且容易产生偏差/假象。在此,我们介绍了一种使用具有多功能特性的工程超顺磁性材料直接分离和随后检测特定外泌体群体的简单方法,该材料即负载金的氧化铁纳米立方(Au-NPFeONC)。在该方法中,首先将 Au-NPFeONC 用通用的四跨膜蛋白(外泌体相关)抗体(即 CD63)进行功能化,并分散在样品流体中,在其中它们作为“可分散纳米载体”来捕获外泌体的大部分群体。在磁性收集和纯化后,将 Au-NPFeONC 结合的外泌体转移到组织特异性、抗体修饰的、丝网印刷电极上。作为原理证明,我们使用了一种特定的胎盘标志物,胎盘碱性磷酸酶(PLAP),来检测来自胎盘细胞的外泌体。然后,Au-NPFeONC 的过氧化物酶样活性用于完成基于酶联免疫吸附测定(ELISA)的检测方案,可通过肉眼观察以及对胎盘细胞条件培养基中存在的 PLAP 特异性外泌体的 UV-可见和电化学检测来实现。我们证明了在使用和不使用商业“总外泌体分离试剂盒”进行预分离步骤的情况下,用于检测胎盘细胞衍生的外泌体的分析性能具有极好的一致性(即线性动态范围,10-10 个外泌体/mL;检测限,10 个外泌体/mL;n = 3 时的相对标准偏差(%RSD)<5.5%)。我们设想,这种高灵敏度、快速且廉价的测定方法可用于定量各种临床应用中外泌体的特定群体,重点关注妊娠并发症。