Precision and Accuracy of Receptor Quantification on Synthetic and Biological Surfaces Using DNA-PAINT.
Roger RieraEmmanouil ArchontakisGlenn CremersTom F A de GreefPeter ZijlstraLorenzo AlbertazziPublished in: ACS sensors (2023)
Characterization of the number and distribution of biological molecules on 2D surfaces is of foremost importance in biology and biomedicine. Synthetic surfaces bearing recognition motifs are a cornerstone of biosensors, while receptors on the cell surface are critical/vital targets for the treatment of diseases. However, the techniques used to quantify their abundance are qualitative or semi-quantitative and usually lack sensitivity, accuracy, or precision. Detailed herein a simple and versatile workflow based on super-resolution microscopy (DNA-PAINT) was standardized to improve the quantification of the density and distribution of molecules on synthetic substrates and cell membranes. A detailed analysis of accuracy and precision of receptor quantification is presented, based on simulated and experimental data. We demonstrate enhanced accuracy and sensitivity by filtering out non-specific interactions and artifacts. While optimizing the workflow to provide faithful counting over a broad range of receptor densities. We validated the workflow by specifically quantifying the density of docking strands on a synthetic sensor surface and the densities of PD1 and EGF receptors (EGFR) on two cellular models.
Keyphrases
- electronic health record
- single molecule
- cell surface
- circulating tumor
- small cell lung cancer
- biofilm formation
- high resolution
- cell free
- single cell
- binding protein
- magnetic resonance imaging
- cell therapy
- tyrosine kinase
- molecular dynamics simulations
- stem cells
- big data
- machine learning
- high throughput
- mass spectrometry
- small molecule
- protein protein
- circulating tumor cells
- label free
- combination therapy
- image quality