Coaxial dual-path electrochemical biosensing and logic strategy-based detection of lung cancer-derived exosomal PD-L1

Nanoscale. 2024 May 9;16(18):8950-8959. doi: 10.1039/d4nr00412d.

Abstract

Exosomal programmed death ligand-1 (ExoPD-L1) is a vital marker of immune activation in the early stages of tumor therapy and it can inhibit anti-tumor immune responses. However, due to the low expression of ExoPD-L1 in cancer cells, it is difficult to perform highly sensitive assays and accurately differentiate cancer sources. Therefore, we constructed a coaxial dual-path electrochemical biosensor for highly accurate identification and detection of ExoPD-L1 from lung cancer based on chemical-biological coaxial nanomaterials and nucleic acid molecular signal amplification strategies. The measurements showed that the detected ExoPD-L1 concentrations ranged from 6 × 102 particles per mL to 6 × 108 particles per mL, and the detection limit was 310 particles per mL. Compared to other sensors, the electrochemical biosensor designed in this study has a lower detection limit and a wider detection range. Furthermore, we also successfully identified lung cancer-derived ExoPD-L1 by analyzing multiple protein biomarkers expressed on exosomes through the "AND" logic strategy. This sensor platform is expected to realize highly sensitive detection and accurate analysis of multiple sources of ExoPD-L1 and provide ideas for the clinical detection of ExoPD-L1.

MeSH terms

  • B7-H1 Antigen* / analysis
  • B7-H1 Antigen* / metabolism
  • Biomarkers, Tumor / analysis
  • Biosensing Techniques* / methods
  • Cell Line, Tumor
  • Electrochemical Techniques*
  • Exosomes* / chemistry
  • Exosomes* / metabolism
  • Humans
  • Limit of Detection
  • Lung Neoplasms* / diagnosis
  • Lung Neoplasms* / metabolism

Substances

  • B7-H1 Antigen
  • CD274 protein, human
  • Biomarkers, Tumor