Zellefrow Crystal D, Griffiths Jennifer S, Saha Sarmistha, Hodges Abby M, Goodman Jessica L, Paulk Joshiawa, Kritzer Joshua A, Schepartz Alanna
Department of Chemistry, Yale University, New Haven, CT 06520-8107, USA.
J Am Chem Soc. 2006 Dec 27;128(51):16506-7. doi: 10.1021/ja0672977.
There is considerable current interest in the design of encodable molecules that regulate intracellular protein circuitry and/or activity, ideally with a high level of specificity. Src homology 3 (SH3) domains are ubiquitous components of multidomain signaling proteins, including many kinases, and are attractive drug targets because of the important role their interactions play in diseases as diverse as cancer, osteoporosis, and inflammation. Here we describe a set of miniature proteins that recognize distinct SH3 domains from Src family kinases with high affinity. Three of these molecules discriminate effectively between the SH3 domains of Src and Fyn, which are expressed ubiquitously, and two of these three activate Hck kinase with potencies that rival HIV Nef, one of the most potent kinase activators known. These results suggest that miniature proteins represent a viable, encodable strategy for selective activation of Src family kinases in a variety of cell types.
目前,人们对可编码分子的设计有着浓厚的兴趣,这些分子能够调节细胞内蛋白质电路和/或活性,理想情况下具有高度的特异性。Src同源3(SH3)结构域是多结构域信号蛋白(包括许多激酶)中普遍存在的组成部分,由于它们的相互作用在癌症、骨质疏松症和炎症等多种疾病中发挥着重要作用,因此是有吸引力的药物靶点。在这里,我们描述了一组微型蛋白质,它们能以高亲和力识别Src家族激酶中不同的SH3结构域。其中三个分子能有效区分普遍表达的Src和Fyn的SH3结构域,这三个分子中的两个能激活Hck激酶,其效力可与已知最有效的激酶激活剂之一HIV Nef相媲美。这些结果表明,微型蛋白质代表了一种可行的、可编码的策略,用于在多种细胞类型中选择性激活Src家族激酶。