Smith David F, Song Xuezheng, Cummings Richard D
Department of Biochemistry, The Glycomics Center, Emory University School of Medicine, Atlanta, Georgia, USA.
Methods Enzymol. 2010;480:417-44. doi: 10.1016/S0076-6879(10)80033-3.
Microarrays of defined glycans represent a high throughput approach to determining the specificity of lectins, or more generally glycan-binding proteins (GBPs). The utility of a glycan microarray is directly related to the number and variety of the glycans available on the printed surface for interrogation by GBPs. The Consortium for Functional Glycomics (CFG), funded by the National Institute of General Medical Sciences (NIGMS), has generated a glycan microarray available to the public as an investigator-driven resource, where hundreds of GBPs have been analyzed. Here we describe the methods generally used by the CFG to prepare glycan arrays and interrogate them with GBPs. We also describe our new approach to normalizing glycan microarray data derived from concentration-dependent analyses of GBP binding, and the application of this approach with the plant lectin Sambucus nigra agglutinin (SNA-I) and human galectin-8. The use of glycan microarrays with this approach readily generates a prediction of the glycan determinants required for high affinity binding by a GBP.
特定聚糖的微阵列代表了一种用于确定凝集素或更一般的聚糖结合蛋白(GBP)特异性的高通量方法。聚糖微阵列的效用与印刷表面上可供GBP检测的聚糖的数量和种类直接相关。由美国国立综合医学科学研究所(NIGMS)资助的功能糖组学联盟(CFG)已生成一种可供公众使用的聚糖微阵列,作为一种由研究者驱动的资源,已有数百种GBP在此进行了分析。本文我们描述了CFG通常用于制备聚糖阵列并用GBP对其进行检测的方法。我们还描述了我们用于对源自GBP结合浓度依赖性分析的聚糖微阵列数据进行归一化的新方法,以及该方法在植物凝集素黑接骨木凝集素(SNA-I)和人半乳糖凝集素-8上的应用。采用这种方法使用聚糖微阵列能够轻松预测GBP高亲和力结合所需的聚糖决定簇。