Chemoenzymatic Synthesis of Sialoglycopolypeptides As Glycomimetics to Block Infection by Avian and Human Influenza Viruses-Reference-Cited by-同舟云学术

Chemoenzymatic Synthesis of Sialoglycopolypeptides As Glycomimetics to Block Infection by Avian and Human Influenza Viruses

Published:2009-02-12 Issue:3 Volume:20 Page:538-549
ISSN:1043-1802
Container-title:Bioconjugate Chemistry
language:en
Short-container-title:Bioconjugate Chem.

Author:

Ogata Makoto¹,Hidari Kazuya I. P. J.¹,Murata Takeomi¹,Shimada Shizumi¹,Kozaki Wataru¹,Park Enoch Y.¹,Suzuki Takashi¹,Usui Taichi¹

Affiliation:

1. Department of Bioscience, Graduate School of Science and Technology, Shizuoka University, Ohya 836, Suruga ward, Shizuoka 422-8529, Japan, Department of Biochemistry, University of Shizuoka, School of Pharmaceutical Sciences and Global COE Program, and Department of Applied Biological Chemistry, Faculty of Agriculture, Shizuoka University

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Pharmaceutical Science,Pharmacology,Biomedical Engineering,Bioengineering,Biotechnology

Link

https://pubs.acs.org/doi/pdf/10.1021/bc800460p

Reference36 articles.

1. Restoration of specific myxovirus receptors to asialoerythrocytes by incorporation of sialic acid with pure sialyltransferases.

2. Human influenza A virus hemagglutinin distinguishes sialyloligosaccharides in membrane-associated gangliosides as its receptor which mediates the adsorption and fusion processes of virus infection. Specificity for oligosaccharides and sialic acids and the sequence to which sialic acid is attached.

3. Receptor binding properties of human and animal H1 influenza virus isolates

4. Specification of Receptor-Binding Phenotypes of Influenza Virus Isolates from Different Hosts Using Synthetic Sialylglycopolymers: Non-Egg-Adapted Human H1 and H3 Influenza A and Influenza B Viruses Share a Common High Binding Affinity for 6′-Sialyl(N-acetyllactosamine)

5. “Multivalent” saccharides: development of new approaches for inhibiting the effects of glycosphingolipid-binding pathogens

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