Key Laboratory of Clinical Laboratory Diagnostics (Ministry of Education), College of Laboratory Medicine, Chongqing Medical University, Chongqing, 400016, China.
Bioscience (Tianjin) Diagnostic Technology CO., LTD, Tianjin, 300000, China.
Biosens Bioelectron. 2020 Apr 15;154:112066. doi: 10.1016/j.bios.2020.112066. Epub 2020 Jan 28.
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 particles/μL 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.
非小细胞肺癌 (NSCLC) 被报道会向血液循环系统中分泌高浓度的外泌体,这是一种用于 NSCLC 早期诊断的敏感且非侵入性生物标志物。但是,目前仍然缺乏可行且准确的方法来分析来自不同 NSCLC 细胞的外泌体。在此,我们通过抗体和不同识别位点的生物亲和力相互作用,构建了一种 SPRi 生物传感分析方法,用于高灵敏度和多重特征化 NSCLC 衍生的外泌体。通过这种方式,可以通过精确识别外泌体蛋白模式,有效区分正常肺和 NSCLC 细胞来源的外泌体。并且,通过抗 CD63、抗 EGFR 和抗 EpCAM 修饰的 SPRi 阵列实现了 NSCLC 相关外泌体的多重特征化。在功能化金纳米粒子的帮助下,这种基于 SPRi 的生物传感器的检测限 (LOD) 可达到 10 个颗粒/μL。此外,该生物传感分析方法已成功应用于临床血浆样本中外泌体的测定。这种 SPRi 生物传感策略可能为临床标本中大量高通量筛选 NSCLC 提供一种潜在的替代方法。