Corson Timothy W, Aberle Nicholas, Crews Craig M
Department of Molecular, Cellular & Developmental Biology, Yale University, New Haven, Connecticut 06511, USA.
ACS Chem Biol. 2008 Nov 21;3(11):677-692. doi: 10.1021/cb8001792.
Induction of protein--protein interactions is a daunting challenge, but recent studies show promise for small molecules that specifically bring two or more protein molecules together for enhanced or novel biological effect. The first such bifunctional molecules were the rapamycin- and FK506-based "chemical inducers of dimerization", but the field has since expanded with new molecules and new applications in chemical genetics and cell biology. Examples include coumermycin-mediated gyrase B dimerization, proteolysis targeting chimeric molecules (PROTACs), drug hybrids, and strategies for exploiting multivalency in toxin binding and antibody recruitment. This Review discusses these and other advances in the design and use of bifunctional small molecules and potential strategies for future systems.
诱导蛋白质-蛋白质相互作用是一项艰巨的挑战,但最近的研究表明,小分子有望将两个或更多蛋白质分子特异性地聚集在一起,以增强或产生新的生物学效应。首批此类双功能分子是基于雷帕霉素和FK506的“二聚化化学诱导剂”,但此后该领域已随着新分子以及在化学遗传学和细胞生物学中的新应用而不断扩展。实例包括香豆霉素介导的促旋酶B二聚化、靶向嵌合分子的蛋白酶解(PROTAC)、药物杂合体,以及在毒素结合和抗体募集方面利用多价性的策略。本综述讨论了双功能小分子设计与应用方面的这些进展及其他进展,以及未来系统的潜在策略。