Erster Oran, Eisenstein Miriam, Liscovitch Mordechai
Department of Biological Regulation, Weizmann Institute of Science, P.O. Box 26, Rehovot 76100, Israel.
Nat Methods. 2007 May;4(5):393-5. doi: 10.1038/nmeth1046. Epub 2007 Apr 22.
The ligand interaction scan (LIScan) method is a general procedure for engineering small molecule ligand-regulated forms of a protein that is complementary to other 'reverse' genetic and chemical-genetic methods for drug-target validation. It involves insertional mutagenesis by a chemical-genetic 'switch', comprising a genetically encoded peptide module that binds with high affinity to a small-molecule ligand. We demonstrated the method with TEM-1 beta-lactamase, using a tetracysteine hexapeptide insert and a biarsenical fluorescein ligand (FlAsH).
配体相互作用扫描(LIScan)方法是一种用于构建小分子配体调控形式蛋白质的通用程序,它与用于药物靶点验证的其他“反向”遗传和化学遗传方法互补。该方法涉及通过化学遗传“开关”进行插入诱变,该“开关”由与小分子配体具有高亲和力结合的基因编码肽模块组成。我们使用四半胱氨酸六肽插入片段和双砷荧光素配体(FlAsH),以TEM-1β-内酰胺酶为例展示了该方法。