首页 | 本学科首页   官方微博 | 高级检索  
     


Discovery of Small‐Molecule Interleukin‐2 Inhibitors from a DNA‐Encoded Chemical Library
Authors:Markus Leimbacher  Dr. Yixin Zhang  Dr. Luca Mannocci  Michael Stravs  Dr. Tim Geppert  Dr. Jörg Scheuermann  Prof. Gisbert Schneider  Prof. Dario Neri
Affiliation:1. Department of Chemistry and Applied Biosciences, Institute of Pharmaceutical Sciences, Wolfgang Pauli‐Str. 10, 8093 Zürich (Switzerland), Fax: (+41)?44‐633‐13‐58;2. Philochem AG, Libernstrasse 3, 8112 Otelfingen (Switzerland)
Abstract:
Libraries of chemical compounds individually coupled to encoding DNA tags (DNA‐encoded chemical libraries) hold promise to facilitate exceptionally efficient ligand discovery. We constructed a high‐quality DNA‐encoded chemical library comprising 30 000 drug‐like compounds; this was screened in 170 different affinity capture experiments. High‐throughput sequencing allowed the evaluation of 120 million DNA codes for a systematic analysis of selection strategies and statistically robust identification of binding molecules. Selections performed against the tumor‐associated antigen carbonic anhydrase IX (CA IX) and the pro‐inflammatory cytokine interleukin‐2 (IL‐2) yielded potent inhibitors with exquisite target specificity. The binding mode of the revealed pharmacophore against IL‐2 was confirmed by molecular docking. Our findings suggest that DNA‐encoded chemical libraries allow the facile identification of drug‐like ligands principally to any protein of choice, including molecules capable of disrupting high‐affinity protein–protein interactions.
Keywords:DNA‐encoded chemical libraries  drug discovery  high‐throughput screening  inhibitors  ligands
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号