Titlebook: Glycovirology; Methods and Protocol Yasuo Suzuki Book 2022 The Editor(s) (if applicable) and The Author(s), under exclusive license to Spri

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,Traditionelle Ans?tze: haben Grenzen!,and mammals determine viral host range, tissue tropism, and pathogenicity. Here, we describe method that allows to characterize binding of IVs to biologically relevant cellular receptors using a conventional solid-phase enzyme-linked assay. In this method, we isolate plasma membranes from respirator

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https://doi.org/10.1007/978-3-322-97140-1ter by utilizing glycoproteins or glycosphingolipids (gangliosides) containing sialic acid on the cell membrane. We developed a solid-phase binding assay to evaluate hPIV-1, hPIV-3, and Sendai virus’ abilities to bind to different types of gangliosides. hPIV1 and hPIV3 show strong binding to neolact

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https://doi.org/10.1007/978-3-322-91508-5r to influenza C virus (ICV), IDV also has seven segments in its genome and has only one major surface glycoprotein, called the hemagglutinin-esterase-fusion (HEF) protein, for receptor-binding, receptor-destroying, and membrane fusion. HEF utilizes 9-O-acetylated sialic acids as its receptor and ha

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Leistungsbewertung als p?dagogische Praktikessary for the efficient transmission of avian influenza viruses among humans. Accordingly, constant monitoring of the receptor-binding specificity of avian influenza viruses is important. In this chapter, we describe the protocol for assessing the receptor-binding specificity of influenza A viruses

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