Label-free detection and molecular profiling of exosomes with a nano-plasmonic sensor

被引:1159
作者
Im, Hyungsoon [1 ]
Shao, Huilin [1 ]
Park, Yong Il [1 ]
Peterson, Vanessa M. [1 ]
Castro, Cesar M. [1 ]
Weissleder, Ralph [1 ,2 ]
Lee, Hakho [1 ]
机构
[1] Massachusetts Gen Hosp, Ctr Syst Biol, Boston, MA 02114 USA
[2] Harvard Univ, Sch Med, Dept Syst Biol, Boston, MA USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
OVARIAN-CANCER; PROTEIN; MARKER; MICROARRAYS; EXPRESSION; KNOWLEDGE; ASCITES; GROWTH; ARRAYS; CD24;
D O I
10.1038/nbt.2886
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 [微生物学]; 090105 [作物生产系统与生态工程];
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.
引用
收藏
页码:490 / U219
页数:9
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