| Literature DB >> 26216389 |
Lin Liu1, Jingying Zha2, Antonio DiGiandomenico2, Douglas McAllister3, C Kendall Stover2, Qun Wang4, Geert-Jan Boons5.
Abstract
All Enterobacteriaceae express a polysaccharide known as enterobacterial common antigen (ECA), which is an attractive target for the development of universally acting immunotherapies. The first chemical synthesis of ECA-derived oligosaccharides for the development of such therapies is described. A number of synthetic challenges had to be addressed, including the development of concise synthetic procedures for unusual monosaccharides, the selection of appropriate orthogonal protecting groups, the development of stereoselective glycosylation methods, appropriate timing for the introduction of the carboxylic acid groups on the ManpNAcA moieties, and the selection of appropriate conditions for the reduction of multiple azido moieties. The synthetic compounds were employed to uncover immunodominant moieties of ECA. Furthermore, a monoclonal antibody (mAb) was developed that binds to ECA and can selectively recognize a wide range of Enterobacteriaceae species.Entities:
Keywords: antigens; enterobacteriaceae; glycosylation; immunotherapy; oligosaccharides
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Year: 2015 PMID: 26216389 PMCID: PMC4664081 DOI: 10.1002/anie.201505420
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336