作者
Corwin M Nycholat, Ryan McBride, Damian C Ekiert, Rui Xu, Janani Rangarajan, Wenjie Peng, Nahid Razi, Michel Gilbert, Warren Wakarchuk, Ian A Wilson, James C Paulson
发表日期
2012/5/14
期刊
Angewandte Chemie International Edition
卷号
51
期号
20
页码范围
4860-4863
出版商
WILEY‐VCH Verlag
简介
The initial stages of an influenzaA virus infection are mediated by the binding of the viral hemagglutinin (HA) to sialylated glycan receptors on host epithelial cells.[1] The specificity of the HA is believed to be a key determinant of viral host range.[2] While all 16 influenza HA subtypes are found in avian viruses, only three are found in viruses adapted to humans (H1, H2, and H3), each resulting in a major pandemic. HAs from avian and human viruses are characterized by their preference for α2-3 and α2-6-linked sialic acids, respectively. Studies now suggest that other elements of sialoglycan sequence are also important factors of HA specificity that contribute to the species barrier.[3] Recently, human and swine respiratory epithelial cells were shown to express sialylated N-linked glycans with extended poly-N-acetyllactosamine (poly-LacNAc) chains.[4] Poly-LacNAc chains are Galβ1-4GlcNAcβ1-3 tandem repeats …
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