Powell Andrew K, Zhi Zheng-Liang, Turnbull Jeremy E
School of Biological Sciences, University of Liverpool, Crown Street, L69 7ZB, Liverpool, UK.
Methods Mol Biol. 2009;534:313-29. doi: 10.1007/978-1-59745-022-5_22.
This chapter describes two methods for fabricating microarrays of saccharides for display and interrogation with binding proteins, using fluorescence detection. The first approach is based on the rapid immobilization of heparan sulphate glycans upon commercially available aminosilane slides via their reducing ends. The second approach is based on the use of a hydrazide-derivatized self-assembled monolayer (SAM) on a gold-coated slide surface. Both provide for efficient and chemoselective attachment and anchoring of oligosaccharide probes via their reducing ends, enabling the large-scale arraying of natural saccharides without cumbersome pre-derivatization. The latter platform, in particular, also has the potential for use with other biophysical readout methods including matrix-assisted laser desorption/ionization time-of-flight mass spectroscopy, surface plasmon resonance, and quartz crystal microbalances. These microarray platforms provide a facile approach for interrogating multiple carbohydrate-protein interactions in a high-throughput manner using minimal quantities of reagents. They provide an essential new experimental strategy in the growing armoury of the glycomics toolkit.
本章介绍了两种用于制备糖类微阵列的方法,以便使用荧光检测与结合蛋白进行展示和相互作用研究。第一种方法是基于硫酸乙酰肝素聚糖通过其还原端快速固定在市售的氨基硅烷载玻片上。第二种方法是基于在镀金载玻片表面使用酰肼衍生的自组装单分子层(SAM)。这两种方法都能通过寡糖探针的还原端实现高效且化学选择性的连接和固定,从而无需繁琐的预衍生化就能大规模排列天然糖类。特别是后一种平台,还具有与其他生物物理读出方法联用的潜力,包括基质辅助激光解吸/电离飞行时间质谱、表面等离子体共振和石英晶体微天平。这些微阵列平台提供了一种简便的方法,可使用少量试剂以高通量方式研究多种碳水化合物 - 蛋白质相互作用。它们在不断发展的糖组学工具库中提供了一种重要的新实验策略。