外体
微泡
适体
纳米探针
化学
液体活检
内化
纳米粒子跟踪分析
纳米技术
计算生物学
癌症研究
小RNA
分子生物学
纳米颗粒
细胞
癌症
生物化学
生物
基因
遗传学
材料科学
作者
Dan Jin,Fan Yang,Yulin Zhang,Li Liu,Yujuan Zhou,Fubing Wang,Guo‐Jun Zhang
出处
期刊:Analytical Chemistry
[American Chemical Society]
日期:2018-10-23
卷期号:90 (24): 14402-14411
被引量:174
标识
DOI:10.1021/acs.analchem.8b03959
摘要
Tumor exosomes that inherit molecular markers from their parent cells are emerging as cellular "surrogates" in cancer diagnostics. Molecular profiling and detection of exosomes offer a noninvasive access to the state of cancer progression, yet are still technically challenging. Here we report an exosome-oriented, aptamer nanoprobe-based profiling (ExoAPP) assay to phenotype surface proteins and quantify cancerous exosomes in a facile mix-and-detect format. Our ExoAPP interfaces graphene oxide (GO) with target-responsive aptamers to profile exosomal markers across five cell types by complementing with enzyme-assisted exosome recycling, revealing a heterogeneous pattern.This assay achieves a detection limit down to 1.6 × 105 particles/mL, lowered by several orders of magnitude over other homogeneous protocols. Such a sensitive ExoAPP assay allows for monitoring epithelial-mesenchymal transition through heterogeneous exosomes without involving cellular internalization that often occurs in GO-based cargo delivery. Using ExoAPP to analyze blood samples from prostate cancer patients, we find that target exosome can be identified by surface PSMA, suggesting their potential in clinical diagnosis.
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