微泡
外体
表面等离子共振
纳米技术
等离子体子
生物
计算生物学
化学
材料科学
纳米颗粒
小RNA
基因
生物化学
光电子学
作者
Hyungsoon Im,Huilin Shao,Yong Il Park,Vanessa M. Peterson,Cesar M. Castro,Ralph Weissleder,Hakho Lee
摘要
Exosomes show potential for cancer diagnostics because they transport molecular contents of the cells from which they originate. Detection and molecular profiling of exosomes is technically challenging and often requires extensive sample purification and labeling. Here we describe a label-free, high-throughput approach for quantitative analysis of exosomes. Our nano-plasmonic exosome (nPLEX) assay is based on transmission surface plasmon resonance through periodic nanohole arrays. Each array is functionalized with antibodies to enable profiling of exosome surface proteins and proteins present in exosome lysates. We show that this approach offers improved sensitivity over previous methods, enables portable operation when integrated with miniaturized optics and allows retrieval of exosomes for further study. Using nPLEX to analyze ascites samples from ovarian cancer patients, we find that exosomes derived from ovarian cancer cells can be identified by their expression of CD24 and EpCAM, suggesting the potential of exosomes for diagnostics.
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