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Glycobiology Advance Access published online on March 5, 2007

Glycobiology, doi:10.1093/glycob/cwm026
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© The Author 2007. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permissions@oxfordjournals.org

Affinity of galectin-8 and its carbohydrate recognition domains for ligands in solution and at the cell surface

Susanne Carlsson1, Christopher T. Öberg2, Michael C Carlsson1, Anders Sundin2, Ulf J. Nilsson2, David Smith3, Richard D. Cummings3, Jenny Almkvist4, Anna Karlsson4 and Hakon Leffler1,*

1 Section of Microbiology Immunology and Glycobiology (MIG), Lund University, 223 62 Lund, Sweden
2 Organic Chemistry, Lund University, 222 41 Lund, Sweden
3 Department of Biochemistry, Emory University School of Medicine, Atlanta, GA 30322, USA
4 The Phagocyte Research Laboratory, Department of Rheumatology and Inflammation Research, Göteborg University, 413 46 Göteborg, Sweden


* To whom correspondence should be addressed: Hakon Leffler, Inst. of Lab Medicine, Sect. of MIG, Sölvegatan 23, S-223 62 Lund, Sweden. E-mail: hakon.leffler{at}med.lu.se. Phone: +46 46-173270. Fax: +46 46-137468

Received on January 19, 2007; revised on February 22, 2007; accepted on February 27, 2007

Galectin-8 has two different carbohydrate recognition domains (CRDs) linked by a peptide, and has various effects on cell adhesion and signalling. To further understand the mechanism for these effects we compared the binding activities of galectin-8 in solution with its binding and activation of cells. We used glycan array analysis to broaden the specificity profile of the two galectin-8 CRDs, as well as intact galectin-8s (short and long linker), confirming the unique preference for sulphated and sialylated glycans of the N-CRD. By a fluorescence anisotropy assay, we examined the solution affinities for a subset of these glycans, the highest being 50 nM for NeuAc{alpha}2,3Lac by galectin-8N. Thus, carbohydrate-protein interactions can be of high affinity without requiring multivalency. More importantly, by fluorescence polarisation we also gained information on how the affinity is built by multiple weak interactions between different fragments of the glycan and its carrier molecule and the galectin CRD subsites (A-E). In intact galectin-8 proteins, the two domains act independently of each other in solution, whereas at a surface they act together. Ligands with moderate or weak affinity for the isolated CRDs on the array are bound strongly by intact galectin-8s. Also galectin-8 binding and signaling at cell surfaces can be explained by combined binding of the two CRDs to low or medium affinity ligands, and their highest affinity ligands, such as sialylated galactosides, are not required.

Key words: Affinity / Cell surface / Galectin / Sialic acid / Specificity


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