ACS Combinatorial Science · 2019 · 90 citations · 23 references
PharmacyMedicinal ChemistryCombinatorial ChemistryDrug DesignDrug DiscoveryChemical Library DesignDna SequencingHigh-throughput ScreeningLibrary ConstructionLibrary ScreeningSmall-molecule ScreeningAffinity SelectionComparative Enrichment AnalysisDna-encoded LibrariesDna-encoded Library SelectionEarly Drug DiscoveryEnrichment AnalysisLibrary AmplificationNormalized Enrichment Score
DNA-encoded chemical libraries (DELs) provide a high-throughput and cost-effective route for screening billions of unique molecules for binding affinity for diverse protein targets. Identifying candidate compounds from these libraries involves affinity selection, DNA sequencing, and measuring enrichment in a sample pool of DNA barcodes. Successful detection of potent binders is affected by many factors, including selection parameters, chemical yields, library amplification, sequencing depth, sequencing errors, library sizes, and the chosen enrichment metric. To date, there has not been a clear consensus about how enrichment from DEL selections should be measured or reported. We propose a normalized z-score enrichment metric using a binomial distribution model that satisfies important criteria that are relevant for analysis of DEL selection data. The introduced metric is robust with respect to library diversity and sampling and allows for quantitative comparisons of enrichment of n-synthons from parallel DEL selections. These features enable a comparative enrichment analysis strategy that can provide valuable information about hit compounds in early stage drug discovery.
23
Philip A. Harris, Bryan W. King, Deepak Bandyopadhyay et al. · Journal of Medicinal Chemistry · 2016 · 275 citations · Full text