Structure-guided design of sialic acid-based Siglec inhibitors and crystallographic analysis in complex with sialoadhesin.

Journal article

The Siglec family of receptors mediates cell surface interactions through recognition of sialylated glycoconjugates. The crystal structure of the N-terminal immunoglobulin-like domain of the Siglec sialoadhesin (SnD1) in complex with 2,3-sialyllactose has informed the design of sialic acid analogs (sialosides) that bind Siglecs with significantly enhanced affinities and specificities. Binding assays against sialoadhesin (Sn; Siglec-1), CD22 (Siglec-2), and MAG (Siglec-4) show a 10- to 300-fold reduction in IC(50) values (relative to methyl-alpha-Neu5Ac) for three sialosides bearing aromatic group modifications of the glycerol side chain: Me-alpha-9-N-benzoyl-amino-9-deoxy-Neu5Ac (BENZ), Me-alpha-9-N-(naphthyl-2-carbonyl)-amino-9-deoxy-Neu5Ac (NAP), and Me-alpha-9-N-(biphenyl-4-carbonyl)-amino-9-deoxy-Neu5Ac (BIP). Crystal structures of these sialosides in complex with SnD1 suggest explanations for the differences in specificity and affinity, providing further ideas for compound design of physiological and potentially therapeutic relevance.

Authors: Zaccai, N; Maenaka, K; Maenaka, T; Crocker, P; Brossmer, R

• Publication status: Published
• Journal: Structure (London, England : 1993)
• Volume: 11
• Issue: 5
• Pages: 557-567
• Publication date: 2003-05-01
• DOI: 10.1016/s0969-2126(03)00073-x
• EISSN: 1878-4186
• ISSN: 0969-2126
• Language: English
• Keywords: Amino Acid Sequence; N-Acetylneuraminic Acid; Protein Structure, Tertiary; Nuclear Proteins; Sialic Acid Binding Immunoglobulin-like Lectins; Receptors, Immunologic; Sialic Acid Binding Ig-like Lectin 1; Crystallography, X-Ray; Lectins; Binding Sites; Membrane Glycoproteins; Molecular Sequence Data