Temme J Sebastian, Krauss Isaac J
Department of Chemistry, Brandeis University, Waltham, Massachusetts.
Curr Protoc Chem Biol. 2015 Jun 1;7(2):73-92. doi: 10.1002/9780470559277.ch140233.
In vitro selection of nucleic acid aptamers, coined SELEX, has led to the discovery of novel therapeutics and aided in the structural and mechanistic understanding of many ligand-biomolecule interactions. A related method, selection with modified aptamers (SELMA), enables selection of DNA aptamers containing bases with a large modification that cannot undergo PCR. A key application of this method is the evolution of aptamers containing carbohydrate modifications. Carbohydrate-binding proteins normally require several copies of the carbohydrate moiety for strong recognition. Whereas it may be difficult to rationally design synthetic scaffolds that cluster glycans in the optimal spacing and orientation for target recognition, SELMA furnishes glycoaptamers with highly optimized glycan clustering, achieving low-nanomolar recognition. Although numerous applications can be envisioned, the protocols and discussions in this article describe procedures involved in applying SELMA to the discovery glycoDNAs that bind to the HIV broadly neutralizing antibody 2G12.
核酸适配体的体外筛选,即指数富集的配体系统进化(SELEX),已促成了新型疗法的发现,并有助于从结构和机制上理解许多配体 - 生物分子相互作用。一种相关方法,即修饰适配体筛选(SELMA),能够筛选出含有无法进行聚合酶链式反应(PCR)的大量修饰碱基的DNA适配体。该方法的一个关键应用是含有碳水化合物修饰的适配体的进化。碳水化合物结合蛋白通常需要几个碳水化合物部分的拷贝才能实现强识别。虽然合理设计能将聚糖以最佳间距和方向聚集以实现靶标识别的合成支架可能很困难,但SELMA能为糖适配体提供高度优化的聚糖聚集,实现低纳摩尔级别的识别。尽管可以设想许多应用,但本文中的方案和讨论描述了将SELMA应用于发现与HIV广谱中和抗体2G12结合的糖DNA所涉及的程序。