Sensitive Signal Amplifying a Diagnostic Biochip Based on a Biomimetic Periodic Nanostructure for Detecting Cancer Exosomes

ACS Appl Mater Interfaces. 2020 Jul 29;12(30):33473-33482. doi: 10.1021/acsami.0c06785. Epub 2020 Jul 14.

Abstract

Tumor-derived exosomes are emerging noninvasive biomarker reservoirs that reflect biological information from their parental cells, especially specific markers, including proteins, DNA fragments and RNAs. Recently, analytical methods of tumor-derived exosomes have been increasing growth. However, developing a convenient signal amplification technique to improve the sensitivity of exosomes detection still remains a challenge. Herein, an ultrasensitive and specific exosomes diagnostic biochip is constructed and further applied to circulating tumor exosomes detection in serum. Using an exosomes diagnostic biochip, signal amplification is achieved by combining the advantages of quantum dots with the biomimetic periodic nanostructure of photonic crystals. Glypican-1 (GPC1), a membrane-anchored protein that is overexpressed in exosomes from pancreatic cancer, is detected using nanosized molecular beacons with high luminescence efficiency; then the signal is amplified through photonic crystals. Moreover, the method allows the quantitative analysis of various disease-specific surface proteins on exosomes. We believe that this exosomes diagnostic biochip is likely to have potential as an effective bioassay, which may be helpful for quantification of disease-specific exosomes in clinical use.

Keywords: GPC1; cancer detection; exosomes; photonic crystals; signal amplification.

MeSH terms

  • Antibodies, Immobilized / chemistry
  • Antibodies, Immobilized / immunology
  • Biomimetics
  • Cell Line
  • Culture Media / chemistry
  • Exosomes / chemistry
  • Exosomes / metabolism*
  • Fluorescent Dyes / chemistry
  • Glypicans / chemistry
  • Glypicans / immunology
  • Glypicans / metabolism
  • Humans
  • Limit of Detection
  • Nanostructures / chemistry*
  • Optical Imaging
  • Pancreatic Neoplasms / diagnosis
  • Pancreatic Neoplasms / metabolism
  • Protein Array Analysis / methods*
  • Quantum Dots / chemistry
  • Reproducibility of Results

Substances

  • Antibodies, Immobilized
  • Culture Media
  • Fluorescent Dyes
  • Glypicans