| Literature DB >> 26985574 |
Willy Decurtins1, Moreno Wichert1, Raphael M Franzini1, Fabian Buller1, Michael A Stravs1, Yixin Zhang1, Dario Neri1, Jörg Scheuermann1.
Abstract
DNA-encoded chemical libraries (DECLs) are collections of organic compounds that are individually linked to different oligonucleotides, serving as amplifiable identification barcodes. As all compounds in the library can be identified by their DNA tags, they can be mixed and used in affinity-capture experiments on target proteins of interest. In this protocol, we describe the screening process that allows the identification of the few binding molecules within the multiplicity of library members. First, the automated affinity selection process physically isolates binding library members. Second, the DNA codes of the isolated binders are PCR-amplified and subjected to high-throughput DNA sequencing. Third, the obtained sequencing data are evaluated using a C++ program and the results are displayed using MATLAB software. The resulting selection fingerprints facilitate the discrimination of binding from nonbinding library members. The described procedures allow the identification of small organic ligands to biological targets from a DECL within 10 d.Entities:
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Year: 2016 PMID: 26985574 PMCID: PMC6126613 DOI: 10.1038/nprot.2016.039
Source DB: PubMed Journal: Nat Protoc ISSN: 1750-2799 Impact factor: 13.491