| Literature DB >> 30503907 |
Takahiro Hiono1, Atsushi Matsuda2, Takanori Wagatsuma3, Masatoshi Okamatsu4, Yoshihiro Sakoda4, Atsushi Kuno5.
Abstract
Glycan structures on hemagglutinin (HA) of influenza A viruses have been analyzed previously to understand their significance. However, the formerly established methods using mass spectrometry present disadvantages such as procedure complexity, sensitivity, and throughput. Our study has established a novel method for analyzing glycan profiles of HA using lectin microarray techniques. We successfully obtained glycan profiles of HA starting from 1 ml of the 106 TCID50 samples through simple antigen enrichment using optimized immunoprecipitation. The profiles were reasonably consistent with known glycan structures of HA. Next, we compared glycan profiles of the HAs prepared from chicken embryos, MDCK, Vero, and A549 cells, and demonstrated the host cell-specific HA glycan profiles. Notably, the HA from MDCK cells was α1-3 galactosylated. Our method provides a highly sensitive and simple procedure for glycan profiling of the viral glycoproteins, thereby paving way for direct glycan analyses of human- and animal-derived virions.Entities:
Keywords: Glycosylation; Hemagglutinin; Influenza A virus; Lectin microarray; α-Gal
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Year: 2018 PMID: 30503907 DOI: 10.1016/j.virol.2018.11.010
Source DB: PubMed Journal: Virology ISSN: 0042-6822 Impact factor: 3.616