Comprehensive Toolkit of Plant Cell Wall Glycan-Directed Monoclonal Antibodies
A collection of 130 new plant cell wall glycan-directed monoclonal antibodies (mAbs) was generated with the aim of facilitating in-depth analysis of cell wall glycans. An enzyme-linked immunosorbent assay-based screen against a diverse panel of 54 plant polysaccharides was used to characterize the b...
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Published in | Plant physiology (Bethesda) Vol. 153; no. 2; pp. 514 - 525 |
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Main Authors | , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
American Society of Plant Biologists
01.06.2010
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Series | Focus Issue on Plant Cell Walls |
Subjects | |
Online Access | Get full text |
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Summary: | A collection of 130 new plant cell wall glycan-directed monoclonal antibodies (mAbs) was generated with the aim of facilitating in-depth analysis of cell wall glycans. An enzyme-linked immunosorbent assay-based screen against a diverse panel of 54 plant polysaccharides was used to characterize the binding patterns of these new mAbs, together with 50 other previously generated mAbs, against plant cell wall glycans. Hierarchical clustering analysis was used to group these mAbs based on the polysaccharide recognition patterns observed. The mAb groupings in the resulting cladogram were further verified by immunolocalization studies in Arabidopsis (Arabidopsis thaliana) stems. The mAbs could be resolved into 19 clades of antibodies that recognize distinct epitopes present on all major classes of plant cell wall glycans, including arabinogalactans (both protein- and polysaccharide-linked), pectins (homogalacturonan, rhamnogalacturonan I), xyloglucans, xylans, mannans, and glucans. In most cases, multiple subclades of antibodies were observed to bind to each glycan class, suggesting that the mAbs in these subgroups recognize distinct epitopes present on the cell wall glycans. The epitopes recognized by many of the mAbs in the toolkit, particularly those recognizing arabinose- and/or galactose-containing structures, are present on more than one glycan class, consistent with the known structural diversity and complexity of plant cell wall glycans. Thus, these cell wall glycan-directed mAbs should be viewed and utilized as epitope-specific, rather than polymer-specific, probes. The current world-wide toolkit of approximately 180 glycan-directed antibodies from various laboratories provides a large and diverse set of probes for studies of plant cell wall structure, function, dynamics, and biosynthesis. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Present address: National Institute of Water and Atmospheric Research Limited, Gate 10 Silverdale Road, Hillcrest, Hamilton 3216, New Zealand. Present address: E*Trade Financial, 4005 Windward Plaza Drive, Alpharetta, GA 30005. This work was supported by the National Science Foundation Plant Genome Program (grant no. DBI–0421683). The author responsible for distribution of materials integral to the findings presented in this article in accordance with the policy described in the Instructions for Authors (www.plantphysiol.org) is: Michael G. Hahn(hahn@ccrc.uga.edu). www.plantphysiol.org/cgi/doi/10.1104/pp.109.151985 Present address: Abeome Corporation, Georgia Biobusiness Center, College Station Road, University of Georgia, Athens, GA 30602. Present address: Department of Foods and Nutrition, Dawson Hall, University of Georgia, Athens, GA 30602. Present address: 907 14th Avenue E, Seattle, WA 98112. Present address: Botany and Plant Sciences, School of Natural Sciences, National University of Ireland-Galway, Galway, Ireland. The online version of this article contains Web-only data. Present address: Industrial Research Limited, P.O. Box 31-310, Lower Hutt 5010, New Zealand. Open Access articles can be viewed online without a subscription. |
ISSN: | 0032-0889 1532-2548 1532-2548 |
DOI: | 10.1104/pp.109.151985 |