Glycan array screening reveals a candidate ligand for Siglec-8

被引:212
作者
Bochner, BS
Alvarez, RA
Mehta, P
Bovin, NV
Blixt, O
White, JR
Schnaar, RL
机构
[1] Johns Hopkins Univ, Sch Med, Div Clin Immunol & Allergy, Baltimore, MD 21224 USA
[2] Univ Oklahoma, Hlth Sci Ctr, Dept Biochem & Mol Biol, Oklahoma City, OK 73104 USA
[3] Oklahoma Med Res Fdn, Cardiovasc Biol Res Program, Oklahoma City, OK 73104 USA
[4] Russian Acad Sci, Shemyakin & Ovchinnikov Inst Bioorgan Chem, Moscow 117901, Russia
[5] Scripps Res Inst, Dept Mol Biol, La Jolla, CA 92037 USA
[6] GlaxoSmithKline, King Of Prussia, PA 19406 USA
[7] Johns Hopkins Univ, Sch Med, Dept Pharmacol & Mol Sci, Baltimore, MD 21205 USA
关键词
D O I
10.1074/jbc.M412378200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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, similar to40 structures were sialylated Among these, avid binding was detected to a single defined glycan, NeuAcalpha-2-3(6-O-sulfo)Galbeta1-4[fucalpha1-3]GlcNAc, also referred to in the literature as 6'-sulfo-sLe(x). Notably, neither unsulfated sLe(x) (NeuAcalpha2-3Galbeta1-4[Fucalpha1-3]GlcNAc) nor an isomer with the sulfate on the 6-position of the GlcNAc residue (6-sulfo-sLe(x), 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 sLe(x) and 6-sulfo-sLe(x) failed to support detectable Siglec-8 binding, 6'-sulfosLe(x) supported significant binding with a K-d of 2.3 mum. 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-sLe(x) of < 5 pmol/spot. In contrast, sLe(x) and 6-sulfo-sLe(x) did not support any Siglec-8 binding at the highest concentration tested (300 pmol/spot). We conclude that Siglec-8 binds preferentially to the sLe(x) structure bearing an additional sulfate ester on the galactose 6-hydroxyl.
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收藏
页码:4307 / 4312
页数:6
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