Profiling cells with DELs: Small molecule fingerprinting of cell surfaces

SLAS Discov. 2024 Jul;29(5):100171. doi: 10.1016/j.slasd.2024.100171. Epub 2024 Jun 23.

Abstract

DNA-encoded small molecule library technology has recently emerged as a new paradigm for identifying ligands against drug targets. To date, it has been used to identify ligands against targets that are soluble or overexpressed on cell surfaces. Here, we report applying cell-based selection methods to profile surfaces of mouse C2C12 myoblasts and myotube cells in an unbiased, target agnostic manner. A panel of on-DNA compounds were identified and confirmed for cell binding selectivity. We optimized the cell selection protocol and employed a novel data analysis method to identify cell selective ligands against a panel of human B and T lymphocytes. We discuss the generality of using this workflow for DNA encoded small molecule library selection and data analysis against different cell types, and the feasibility of applying this method to profile cell surfaces for biomarker and target identification.

Keywords: Affinity selection; Biomarker; Cell profiling; DNA encoded library technology; Proteomics; Theranostics.

MeSH terms

  • Animals
  • B-Lymphocytes / drug effects
  • B-Lymphocytes / metabolism
  • Cell Line
  • Cell Membrane / drug effects
  • Cell Membrane / metabolism
  • Drug Discovery / methods
  • Humans
  • Ligands
  • Mice
  • Myoblasts / drug effects
  • Myoblasts / metabolism
  • Small Molecule Libraries* / pharmacology
  • T-Lymphocytes / drug effects
  • T-Lymphocytes / metabolism

Substances

  • Small Molecule Libraries
  • Ligands