Lane 1: RD cell membrane extracts; Lane 2: MAA/SNA lectin affinit

Lane 1: RD cell membrane extracts; Lane 2: MAA/SNA lectin affinity chromatography

purified sialylated glycoproteins; Lane 3: desialylated https://www.selleckchem.com/products/Ispinesib-mesilate(SB-715992).html glycoproteins; Lane 4: desialylated glycoproteins immunoprecipitated with EV71 MP4. All of the purified proteins were subjected to western blotting and stained by anti-SCARB2 antibody. SCARB2 could be observed in all of the fractions. Band in lane 3 was slightly shifted down after neuraminidase treatment. But, owing to non-reducing condition, band in lane 4 was slightly shifted up compared to band in lane 3. Figure 9 Interactions between recombinant hSCARB2 with EV71 are reduced after desialylation. The binding is detected by Viral-Overlaying Protein Binding Assay (VOPBA) with anti-EV71 antibody and HRP conjugated anti-mouse antibody

on LAS-3000. Discussion Glycans that expressed on cell surface are involved in cell-cell adhesion, leukocyte rolling, cell-extracellular matrix interaction, and microbes’ infection [31–33]. Carbohydrates, especially sialic acids, are also reported as receptors for gram positive or negative selleck products bacteria, viruses, protozoa, and plant lectins [28]. For example, sialyl Lewisx is a ligand for the SabA protein of Helicobacter HTS assay pylori[34]. Cholera toxin of Vibrio chlolerae specifically binds to the GM1 moiety [35]. Human influenza virus recognizes α2-6 sialylated glycans and infects host cells subsequently [36, 37]. Glycosaminoglycan, such as hyaluronic acid and chondroitin sulfate, are confirmed as antiviral agents in preventing Coxsackievirus B5 and dengue virus, respectively [38, 39]. Further,

sialic acid is reported as receptors of many Picornaviridae viruses [28, 29]. Several methods were established to evaluate the attachment and reproduction efficiency of EV71. ELISA assay and flow cytometry provided reliable and reproducible results in quantifying bound EV71 viral particles on cell surface. The binding and subsequent replication of EV71 was detected by measuring the copy number of viral RNA by real-time PCR. In addition, the infection and replication of EV71 could also be confirmed by observing the fluorescence intensity and cytopathic effects in EV71-GFP infected cells. RD is an EV71 highly susceptible cell line which has been applied for viral replication. SK-N-SH cells established from human neuroblastoma were cell second model for investigating the EV71 caused neuron toxicity. RD and SK-N-SH cells were infected with EV71 MP4 (mouse adapted strain) and EV71 4643 (human clinical isolates), respectively [40]. Since glycosylation was a common and significant feature for cellular and functional receptors of EV71, we first investigated the effects of tunicamycin and benzyl-α-GalNAc (inhibitor for protein N- and O-glycosylation, respectively) in the binding and infection of EV71 to RD cells. Both of the inhibitors decreased the binding of EV71 to RD cells significantly (data not shown).

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