Nanoplasmonic Sandwich Immunoassay for Tumor-Derived Exosome Detection and Exosomal PD-L1 Profiling.
Chuanyu WangChung-Hui HuangZhuangqiang GaoJialiang ShenJiacheng HeAlana MacLachlanChao MaYa ChangWen YangYuxin CaiYang LouSiyuan DaiWeiqiang ChenFeng LiPengyu ChenPublished in: ACS sensors (2021)
Tumor-derived exosomes play a vital role in the process of cancer development. Quantitative analysis of exosomes and exosome-shuttled proteins would be of immense value in understanding cancer progression and generating reliable predictive biomarkers for cancer diagnosis and treatment. Recent studies have indicated the critical role of exosomal programmed death ligand 1 (PD-L1) in immune checkpoint therapy and its application as a patient stratification biomarker in cancer immunotherapy. Here, we present a nanoplasmonic exosome immunoassay utilizing gold-silver (Au@Ag) core-shell nanobipyramids and gold nanorods, which form sandwich immune complexes with target exosomes. The immunoassay generates a distinct plasmonic signal pattern unique to exosomes with specific exosomal PD-L1 expression, allowing rapid, highly sensitive exosome detection and accurate identification of PD-L1 exosome subtypes in a single assay. The developed nanoplasmonic sandwich immunoassay provides a novel and viable approach for tumor cell-derived exosome detection and analysis with quantitative molecular details of key exosomal proteins, manifesting its great potential as a transformative diagnostic tool for early cancer detection, prognosis, and post-treatment monitoring.
Keyphrases
- label free
- papillary thyroid
- loop mediated isothermal amplification
- mesenchymal stem cells
- sensitive detection
- squamous cell
- stem cells
- real time pcr
- gold nanoparticles
- lymph node metastasis
- case report
- high throughput
- risk assessment
- silver nanoparticles
- single molecule
- climate change
- combination therapy
- mass spectrometry
- molecularly imprinted
- liquid chromatography
- tandem mass spectrometry