Arakelyan Anush, Fitzgerald Wendy, Zicari Sonia, Vagida Murad, Grivel Jean-Charles, Margolis Leonid
Section on Intercellular Interactions, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health.
Laboratory of Atherothrombosis, Cardiology Department, Moscow State University of Medicine and Dentistry.
J Vis Exp. 2017 Jan 25(119):55020. doi: 10.3791/55020.
Cells release small extracellular vesicles (EVs) into the surrounding media. Upon virus infection cells also release virions that have the same size of some of the EVs. Both virions and EVs carry proteins of the cells that generated them and are antigenically heterogeneous. In spite of their diversity, both viruses and EVs were characterized predominantly by bulk analysis. Here, we describe an original nanotechnology-based high throughput method that allows the characterization of antigens on individual small particles using regular flow cytometers. Viruses or extracellular vesicles were immunocaptured with 15 nm magnetic nanoparticles (MNPs) coupled to antibodies recognizing one of the surface antigens. The captured virions or vesicles were incubated with fluorescent antibodies against other surface antigens. The resultant complexes were separated on magnetic columns from unbound antibodies and analyzed with conventional flow cytometers triggered on fluorescence. This method has wide applications and can be used to characterize the antigenic composition of any viral- and non-viral small particles generated by cells in vivo and in vitro. Here, we provide examples of the usage of this method to evaluate the distribution of host cell markers on individual HIV-1 particles, to study the maturation of individual Dengue virions (DENV), and to investigate extracellular vesicles released into the bloodstream.
细胞会向周围培养基中释放小细胞外囊泡(EVs)。病毒感染细胞后,细胞还会释放出一些与某些EVs大小相同的病毒粒子。病毒粒子和EVs都携带产生它们的细胞的蛋白质,并且在抗原性上是异质的。尽管它们具有多样性,但病毒和EVs主要都是通过整体分析来表征的。在这里,我们描述了一种基于纳米技术的原创高通量方法,该方法允许使用常规流式细胞仪对单个小颗粒上的抗原进行表征。病毒或细胞外囊泡用与识别一种表面抗原的抗体偶联的15纳米磁性纳米颗粒(MNPs)进行免疫捕获。将捕获的病毒粒子或囊泡与针对其他表面抗原的荧光抗体一起孵育。所得复合物通过磁柱与未结合的抗体分离,并使用基于荧光触发的传统流式细胞仪进行分析。该方法具有广泛的应用,可用于表征体内和体外细胞产生的任何病毒和非病毒小颗粒的抗原组成。在这里,我们提供了该方法的使用示例,以评估宿主细胞标志物在单个HIV-1颗粒上的分布,研究单个登革病毒粒子(DENV)的成熟过程,以及研究释放到血液中的细胞外囊泡。