Tyramide-conjugated DNA barcodes enable signal amplification for multiparametric CODEX imaging.
Paul D SimonsonItzel ValenciaSanjay S PatelPublished in: Communications biology (2022)
Multiparametric imaging allows researchers to measure the expression of many biomarkers simultaneously, allowing detailed characterization of cell microenvironments. One such technique, CODEX, allows fluorescence imaging of >30 proteins in a single tissue section. In the commercial CODEX system, primary antibodies are conjugated to DNA barcodes. This modification can result in antibody dysfunction, and development of a custom antibody panel can be very costly and time consuming as trial and error of modified antibodies proceeds. To address these challenges, we developed novel tyramide-conjugated DNA barcodes that can be used with primary antibodies via peroxidase-conjugated secondary antibodies. This approach results in signal amplification and imaging without the need to conjugate primary antibodies. When combined with commercially available barcode-conjugated primary antibodies, we can very quickly develop working antibody panels. We also present methods to perform antibody staining using a commercially available automated tissue stainer and in situ hybridization imaging on a CODEX platform. Future work will include application of the combined tyramide-based and regular CODEX approach to image specific tumors with their immune cell infiltrates, including biomarkers that are currently difficult to image by regular CODEX.
Keyphrases
- fluorescence imaging
- photodynamic therapy
- high resolution
- nucleic acid
- circulating tumor
- single molecule
- cell free
- high throughput
- clinical trial
- machine learning
- oxidative stress
- stem cells
- randomized controlled trial
- study protocol
- single cell
- nitric oxide
- mass spectrometry
- cell therapy
- mesenchymal stem cells
- hydrogen peroxide
- cancer therapy
- binding protein
- phase iii
- double blind