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Product Name | Recombinant Lake Victoria marburgvirus Envelope glycoprotein (GP), partial |
Description | Purity > 85% as determined by SDS-PAGE. MW: 34.3kDa. Partial: 436-681aa. N-terminal 10xHis-tagged and C-terminal Myc-tagged. Lake Victoria marburgvirus (strain Popp-67) (MARV) (Marburg virus (strain West Germany/Popp/1967)). GP1 is responsible for binding to the receptor on target cells. Interacts with CD209/DC-SIGN and CLEC4M/DC-SIGNR which act as cofactors for virus entry into the host cell. Binding to CD209 and CLEC4M, which are respectively found on dendritic cells, and on endothelial cells of liver sinusoids and lymph node sinuses, facilitate infection of macrophages and endothelial cells. These interactions not only facilitate virus cell entry, but also allow capture of viral particles by DCs and subsequent transmission to susceptible cells without DCs infection.GP2 acts as a class I viral fusion protein. Under the current model, the protein has at least 3 conformational states: pre-fusion native state, pre-hairpin intermediate state, and post-fusion hairpin state. During viral and target cell membrane fusion, the coiled coil regions assume a trimer-of-hairpins structure, positioning the fusion peptide in close proximity to the C-terminal region of the ectodomain. The formation of this structure appears to drive apposition and subsequent fusion of viral and target cell membranes. Responsible for penetration of the virus into the cell cytoplasm by mediating the fusion of the membrane of the endocytosed virus particle with the endosomal membrane. Low pH in endosomes induces an irreversible conformational change in GP2, releasing the fusion hydrophobic peptide. |
Size | 100ug |
Concentration | n/a |
Applications | RUO |
Other Names | GP1,2 (GP) (Virion spike glycoprotein) |
Gene, Accession, CAS # | GP, UniProt: P35254 |
Catalog # | RPC26062 |
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Order / More Info | Recombinant Lake Victoria marburgvirus Envelope glycoprotein (GP), partial from BIOMATIK |
Product Specific References | n/a |
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