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Oligosaccharide Mimetics Obtained by Novel, Rapid Screening of Carboxylic Acid Encoded Glycopeptide Libraries
Glycopeptides that mimic the action of oligosaccharides have been rapidly identified through the implementation of combinatorial library methodology combined with a novel, easy, screening and analysis method. A glycopeptide library containing three different glycosyl amino building blocks, Fmoc-Asn(...
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Published in: | Journal of the American Chemical Society 1998-12, Vol.120 (51), p.13312-13320 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Glycopeptides that mimic the action of oligosaccharides have been rapidly identified through the implementation of combinatorial library methodology combined with a novel, easy, screening and analysis method. A glycopeptide library containing three different glycosyl amino building blocks, Fmoc-Asn(β-Ac3GlcNAc)-OPfp (5), Fmoc-Thr(α-Ac4Man)-OPfp (6), and Fmoc-Thr[α-Ac4Man(1→3)α-2-O-Bz-4,6-Ac2Man]-OPfp (7), was synthesized by the portion-mixing method on PEGA solid support. The library was designed to facilitate rapid and unambiguous analysis of the active glycopeptides detected during the high throughput-screening step. Consequently, the library was synthesized using the ladder synthesis approach and linked to the solid support via a photolabile linker. The glycosyl amino acids were labeled with carboxylic acid tags to allow unambiguous identification of the glycan moiety. Photolytic release of active glycopeptide from the resin was induced by irradiation of the bead with the MALDI-TOF-MS laser, and analysis of the resulting spectrum presenting the ladder of glycopeptide fragments yielded the sequence of the active glycopeptide. Glycopeptide ligands were identified for the C-type lectin from Lathyrus odoratus by screening the fluorescent-labeled protein in a solid-phase binding assay of the PEGA resin-bound glycopeptide library. Of the several glycopeptide ligands detected, most contained Man or GlcNAc, glycans that display specificity for the lectin in hemagglutination assays. The most active glycopeptides detected from the library screening were T(α-d-Man)ALKPTHV, LHGGFT(α-d-Man)HV, T(α-d-Man)EHKGSKV, GT(α-d-Man)FPGLAV, and T(α-d-Man)LFKGFHV. |
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ISSN: | 0002-7863 1520-5126 |
DOI: | 10.1021/ja980387u |