Zuckermann R N, Martin E J, Spellmeyer D C, Stauber G B, Shoemaker K R, Kerr J M, Figliozzi G M, Goff D A, Siani M A, Simon R J
Chiron Corporation, Emeryville, California 94608.
J Med Chem. 1994 Aug 19;37(17):2678-85. doi: 10.1021/jm00043a007.
Screening a diverse, combinatorial library of ca. 5000 synthetic dimer and trimer N-(substituted)glycine "peptides" yielded novel, high-affinity ligands for 7-transmembrane G-protein-coupled receptors. The peptoid library was efficiently assembled using readily available chemical building blocks. The choice of side chains was biased to resemble known ligands to 7-transmembrane G-protein-coupled receptors. All peptides were screened in solution-phase, competitive radioligand-binding assays. Peptoid trimer CHIR 2279 binds to the alpha 1-adrenergic receptor with a Ki of 5 nM, and trimer CHIR 4531 binds to the mu-opiate receptor with a Ki of 6 nM. This represents the first example of the discovery of high-affinity receptor ligands from a combinatorial library of non-natural chemical entities.
对约5000种合成二聚体和三聚体N-(取代)甘氨酸“肽”的多样化组合文库进行筛选,得到了针对7跨膜G蛋白偶联受体的新型高亲和力配体。使用容易获得的化学构建块高效组装了类肽文库。侧链的选择偏向于类似于已知的7跨膜G蛋白偶联受体配体。所有肽均在溶液相竞争性放射性配体结合试验中进行筛选。类肽三聚体CHIR 2279以5 nM的Ki值与α1-肾上腺素能受体结合,三聚体CHIR 4531以6 nM的Ki值与μ-阿片受体结合。这是从非天然化学实体的组合文库中发现高亲和力受体配体的首个实例。