Selection of DNA-Encoded Small Molecule Libraries Against Unmodified and Non-Immobilized Protein Targets

被引:87
作者
Zhao, Peng [5 ]
Chen, Zitian [6 ]
Li, Yizhou [5 ]
Sun, Dawei [5 ]
Gao, Yuan [5 ]
Huang, Yanyi [3 ,4 ]
Li, Xiaoyu [1 ,2 ]
机构
[1] Peking Univ, Coll Chem & Mol Engn, Key Lab Bioorgan Chem & Mol Engn, Beijing 100871, Peoples R China
[2] Peking Univ, Shenzhen Grad Sch, Sch Chem Biol & Biotechnol, Key Lab Chem Genom, Shenzhen 518055, Peoples R China
[3] Peking Univ, Biodynam Opt Imaging Ctr BIOPIC, Beijing 100871, Peoples R China
[4] Peking Univ, Coll Engn, Beijing 100871, Peoples R China
[5] Peking Univ, Coll Chem & Mol Engn, Beijing 100871, Peoples R China
[6] Peking Univ, Coll Engn, Beijing 100871, Peoples R China
关键词
DNA; DNA-encoded library; DNA-templated chemistry; drug discovery; selection; IN-VITRO SELECTION; TERMINAL PROTECTION; BINDING PROTEINS; PEPTIDE LIBRARY; LINKED DNA; DISCOVERY; IDENTIFICATION; ASSAY; PCR; EXONUCLEASE;
D O I
10.1002/anie.201404830
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The selection of DNA-encoded libraries against biological targets has become an important discovery method in chemical biology and drug discovery, but the requirement of modified and immobilized targets remains a significant disadvantage. With a terminal protection strategy and ligand-induced photo-crosslinking, we show that iterated selections of DNA-encoded libraries can be realized with unmodified and non-immobilized protein targets.
引用
收藏
页码:10056 / 10059
页数:4
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