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Cited by 159

The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.

Chemical Synthesis of a Glycoprotein Having an Intact Human Complex-Type Sialyloligosaccharide under the Boc and Fmoc Synthetic Strategies

Yamamoto, Naoki, Tanabe, Yasutaka, Okamoto, Ryo, Dawson, Philip E., Kajihara, Yasuhiro·2008·Journal of the American Chemical Society

Abstract

The chemical synthesis of complex glycoproteins is an ongoing challenge in protein chemistry. We have examined the synthesis of a single glycoform of monocyte chemotactic protein-3 (MCP-3), a CC-chemokine that consists of 76 amino acids and one N-glycosylation site. A three-segment native chemical ligation strategy was employed using unprotected peptides and glycopeptide. Importantly, the synthesis required the development of methods for the generation of sialylglycopeptide-alphathioesters. For the sialylglycopeptide-alphathioester segment, we examined and successfully implemented approaches using Fmoc-SPPS and Boc-SPPS. To avoid use of hydrogen fluoride, the Boc approach utilized minimal side chain protection and direct thiolysis of the resin bound peptide. Using these strategies, we successfully synthesized a glycoprotein having an intact and homogeneous complex-type sialyloligosaccharide.

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Metadata

Authors
Yamamoto, N., Tanabe, Y., Okamoto, R., Dawson, P. E., & Kajihara, Y.
Venue
Journal of the American Chemical Society
Published
2007-12-18
Volume
130
Issue
2
Pages
501-510
ISSN
  • 0002-7863 (ISSN-L)
  • 1520-5126
OpenAlex
W1974599312
Cited by
159
References
2
FWCI
9.83
Type
journal article
Language
en
Open access
closed

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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