The DOI matches its Crossref record; 37 of the 37 references it cites were found in a registry or an index.
Glycan Array Screening Reveals a Candidate Ligand for Siglec-8*
Open accessAbstract
Sialic acid-binding immunoglobulin-like lectin 8 (Siglec-8) is selectively expressed on human eosinophils, basophils, and mast cells, where it regulates their function and survival. Previous studies demonstrated sialic acid-dependent binding of Siglec-8 but failed to reveal significant substructure specificity or high affinity of that binding. To test a broader range of potential ligands, a Siglec-8-Ig chimeric protein was tested for binding to 172 different glycan structures immobilized as biotinylated glycosides on a 384-well streptavidin-coated plate. Of these, approximately 40 structures were sialylated. Among these, avid binding was detected to a single defined glycan, NeuAcalpha2-3(6-O-sulfo)Galbeta1-4[Fucalpha1-3]GlcNAc, also referred to in the literature as 6'-sulfo-sLex. Notably, neither unsulfated sLex (NeuAcalpha2-3Galbeta1-4[Fucalpha1-3]GlcNAc) nor an isomer with the sulfate on the 6-position of the GlcNAc residue (6-sulfo-sLex, NeuAcalpha2-3Galbeta1-4[Fucalpha1-3](6-O-sulfo)GlcNAc) supported detectable binding. Subsequent secondary screening was performed using surface plasmon resonance. Biotin glycosides immobilized on streptavidin biosensor chips were exposed to Siglec-8-Ig in solution. Whereas surfaces derivatized with sLex and 6-sulfo-sLex failed to support detectable Siglec-8 binding, 6'-sulfo-sLex supported significant binding with a Kd of 2.3 microm. In a separate test of binding specificity, aminopropyl glycosides were covalently immobilized at different concentrations on activated (N-hydroxysuccinimidyl) glass surfaces (Schott-Nexterion Slide H). Subsequent exposure to Siglec-8-Ig precomplexed with fluorescein isothiocyanate anti-human Fc resulted in fluorescent signals at immobilized concentrations of 6'-sulfo-sLex of <5 pmol/spot. In contrast, sLex and 6-sulfo-sLex did not support any Siglec-8 binding at the highest concentration tested (300 pmol/spot). We conclude that Siglec-8 binds preferentially to the sLex structure bearing an additional sulfate ester on the galactose 6-hydroxyl.
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Citations
Cites
Siglecs, sialic acids and innate immunity
Crocker, P. R., & Varki, A. (2001) · Trends in Immunology · doi:10.1016/s1471-4906(01)01930-5 · Cited by 382
Siglecs: sialic-acid-binding immunoglobulin-like lectins in cell–cell interactions and signalling
Crocker, P. (2002) · Current Opinion in Structural Biology · doi:10.1016/s0959-440x(02)00375-5 · Cited by 312
Sulfotransferases in glycosaminoglycan biosynthesis
Kusche-Gullberg, M. (2003) · Current Opinion in Structural Biology · doi:10.1016/j.sbi.2003.08.002 · Cited by 307
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Ligation of Siglec-8: a selective mechanism for induction of human eosinophil apoptosis
Nutku, E., Aizawa, H., Hudson, S. A., & Bochner, B. S. (2003) · Blood · doi:10.1182/blood-2002-10-3058 · Cited by 303
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Sialoside Specificity of the Siglec Family Assessed Using Novel Multivalent Probes
Blixt, O., Collins, B. E., van den Nieuwenhof, I. M., Crocker, P. R., & Paulson, J. C. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m304331200 · Cited by 245
Self-citation
Cited by
Siglec-mediated regulation of immune cell function in disease
Macauley, M. S., Crocker, P. R., & Paulson, J. C. (2014) · Nature Reviews Immunology · doi:10.1038/nri3737 · Cited by 1,122
Protein Glycosylation in Cancer
Stowell, S. R., Ju, T., & Cummings, R. D. (2015) · Annual Review of Pathology: Mechanisms of Disease · doi:10.1146/annurev-pathol-012414-040438 · Cited by 873
Advances in the Biology and Chemistry of Sialic Acids
Chen, X., & Varki, A. (2010) · ACS Chemical Biology · doi:10.1021/cb900266r · Cited by 543
The repertoire of glycan determinants in the human glycome
Cummings, R. D. (2009) · Molecular BioSystems · doi:10.1039/b907931a · Cited by 487
Siglecs as Immune Cell Checkpoints in Disease
Duan, S., & Paulson, J. C. (2020) · Annual Review of Immunology · doi:10.1146/annurev-immunol-102419-035900 · Cited by 452
Metadata
- Authors
- Bochner, B. S., Alvarez, R. A., Mehta, P., Bovin, N. V., Blixt, O., White, J. R., & Schnaar, R. L.
- Venue
- Journal of Biological Chemistry
- Publisher
- Elsevier BV
- Published
- 2005-02
- Volume
- 280
- Issue
- 6
- Pages
- 4307-4312
- ISSN
- 0021-9258 (ISSN-L)
- OpenAlex
- W2077521688
- Cited by
- 262
- References
- 37
- FWCI
- 5.79
- Type
- journal article
- Language
- en
- Open access
- hybrid
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- Bochner, B. S., Alvarez, R. A., Mehta, P., Bovin, N. V., Blixt, O., White, J. R., & Schnaar, R. L. (2005). Glycan Array Screening Reveals a Candidate Ligand for Siglec-8*. Journal of Biological Chemistry. https://doi.org/10.1074/jbc.m412378200
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