Preparation and Analysis of Glycan Microarrays
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- Abstract
- Table of Contents
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- Literature Cited
Abstract
Determination of the binding specificity of glycan?binding proteins (GBPs), such as lectins, antibodies, and receptors, has traditionally been difficult and laborious. The advent of glycan microarrays has revolutionized the field of glycobiology by allowing simultaneous screening of a GBP for interactions with a large set of glycans in a single format. This unit describes the theory and method for production of two types of glycan microarrays (chemo/enzymatically synthesized and naturally derived), and their application to functional glycomics to explore glycan recognition by GBPs. These procedures are amenable to various types of arrays and a wide range of GBP samples. Curr. Protoc. Protein Sci. 64:12.10.1?12.10.29. © 2011 by John Wiley & Sons, Inc.
Keywords: glycan microarrays; natural glycan microarrays; glycan?binding specificities; Consortium for Functional Glycomics
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- Introduction
- Basic Protocol 1: The Binding Specificity of Biotinylated Plant Lectins Detected with Fluorescent Streptavidin
- Alternate Protocol 1: Detecting the Glycan Epitopes for Mouse Monoclonal Antibodies Using Fluorescent Anti‐Mouse IgG
- Alternate Protocol 2: Specificity of Directly Labeled Influenza Virus Binding to Sialylated Glycans
- Generation of Natural Glycan Arrays
- Basic Protocol 2: Preparation of a Natural Glycan Microarray
- Basic Protocol 3: Binding Assay for Natural, Defined Glycan Microarray
- Reagents and Solutions
- Commentary
- Literature Cited
- Figures
- Tables
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Basic Protocol 1: The Binding Specificity of Biotinylated Plant Lectins Detected with Fluorescent Streptavidin
Materials
Alternate Protocol 1: Detecting the Glycan Epitopes for Mouse Monoclonal Antibodies Using Fluorescent Anti‐Mouse IgG
Alternate Protocol 2: Specificity of Directly Labeled Influenza Virus Binding to Sialylated Glycans
Basic Protocol 2: Preparation of a Natural Glycan Microarray
Materials
Basic Protocol 3: Binding Assay for Natural, Defined Glycan Microarray
Materials
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Figure 12.10.1 Preparation of natural glycan microarrays. After isolating the glycans from a natural source, they are labeled with a bifunctional fluorescent dye (e.g., AEAB), captured on glass slides, and interrogated by glycan‐binding proteins (GBPs). View Image -
Figure 12.10.2 Schematic of natural, defined glycan array printed with 14 identical subarrays per slide. A multi‐chamber adapter can be placed over the slide surface to create 14 individual chambers for 14 different, simultaneous assays. In this example, each of the 40 glycans is printed in replicates of 4. In some cases, the printed compounds include controls such as glycopeptides and biotin. View Image -
Figure 12.10.3 Con A binding to the CFG glycan array. The top panel is an image of fluorescently detected Con A binding to the glycan array slide. The replicates of one set of 6 spots, corresponding to one glycan, are noted. The bottom panel is a histogram of quantified Con A binding to the glycan array, where the x ‐axis is the chart number (glycan number) and the y ‐axis is relative fluorescent units (RFU). View Image -
Figure 12.10.4 The binding of biotinylated SNA to a natural glycan array containing 52 GAEABs and four controls. After obtaining a fluorescent image of the biotinylated SNA bound by cyanine5‐streptavidin, binding is quantified and displayed as a histogram of the average RFU bound to each glycan. The eight glycan structures that were bound by SNA are displayed next to their respective peak. View Image
Videos
Literature Cited
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