High-sensitive and multiplex biosensing assay of NSCLC-derived exosomes via different recognition sites based on SPRi array

被引:83
作者
Fan, Yunpeng [1 ]
Duan, Xiaolei [1 ]
Zhao, Min [1 ]
Wei, Xiaotong [1 ]
Wu, Jiangling [1 ]
Chen, Wenqin [1 ]
Liu, Ping [2 ]
Cheng, Wei [3 ]
Cheng, Quan [4 ]
Ding, Shijia [1 ]
机构
[1] Chongqing Med Univ, Coll Lab Med, Key Lab Clin Lab Diagnost, Minist Educ, Chongqing 400016, Peoples R China
[2] Biosci Tianjin Diagnost Technol CO LTD, Tianjin 300000, Peoples R China
[3] Chongqing Med Univ, Ctr Clin Mol Med Detect, Affiliated Hosp 1, Chongqing 400016, Peoples R China
[4] Univ Calif Riverside, Dept Chem, Riverside, CA 92521 USA
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
Exosomes; Non-small cell lung cancer; Surface plasmon resonance imaging; Functionalized gold nanoparticles; Biosensing assay; SURFACE-PLASMON RESONANCE; CELL LUNG-CANCER; EXTRACELLULAR VESICLES; EXPRESSION; PROTEINS; IMMUNOASSAY; BIOLOGY;
D O I
10.1016/j.bios.2020.112066
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Non-small cell lung cancer (NSCLC) have been reported to secret a high concentration of exosomes into blood circulatory system, which is one of sensitive and non-invasive biomarkers for NSCLC's early-stage diagnosis. But it is still lack of feasible and accurate methods to analyze the different NSCLC cells-derived exosomes. Herein, we built a SPRi biosensing assay for high-sensitive and multiplex characterizations of NSCLC-derived exosomes by bioaffinity interactions of antibodies and different recognition sites. By this way, the exosomes derived from normal lung and NSCLC cells can be effectively distinguished through precise identification of the exosomal protein pattern. And the multiplex characterizations of NSCLC-related exosomes are also achieved by anti-CD63, anti-EGFR and anti-EpCAM modified SPRi array. The limit of detection (LOD) of this SPRi-based biosensor approaches to the level of 10(4) particles/mu L with the help of functionalized gold nanoparticles. Besides, the developed biosensing assay was successfully applied in the determination of exosomes purified from clinical plasma samples. This SPRi biosensing strategy might offer a potential alternative for massive high-throughput screening for NSCLC in clinical specimens.
引用
收藏
页数:7
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