重组HIV1 + HIV2 envelope antigen蛋白
Recombinant HIV1 + HIV2 envelope antigen protein
Be the first to review this product! Submit a review
|
(0 Publication)
Recombinant HIV1 + HIV2 envelope antigen protein is a Human immunodeficiency virus type 1 (NDK ISOLATE) Fragment protein, expressed in Escherichia coli, with >95%, suitable for ELISA, WB.
查看别名
Envelope glycoprotein gp160, Env polyprotein, env
反应性数据
产品详情
序列信息
性能和储存信息
运输条件
推荐的短期储存条件
推荐的长期储存条件
分装信息
储存信息
补充信息
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
The envelope antigen triggers immune response by presenting itself as a target for antibodies and T cells. Env protein forms part of a larger viral membrane complex critical in maintaining structural integrity and functional virulence of the virus. It engages with CD4 receptors and coreceptors on host cells like CCR5 or CXCR4 determining cell tropism and influencing viral pathogenesis in the immune system. Its presence significantly impacts the progression and severity of HIV infection.
Pathways
The envelope antigen is pivotal in the viral entry and fusion pathways. These pathways contribute key roles in the life cycle of both HIV1 and HIV2. Interaction of gp120 with its CD4 receptor and coreceptors facilitates the conformational changes necessary for gp41-mediated membrane fusion. This interaction is deeply intertwined with normal immune signalling pathways making it closely associated with human proteins like chemokine receptors such as CCR5 which are co-receptors.
特殊说明
形式
Liquid
附加说明
S-Sepharose > Ceramic Hydroxyapatite > S-300 > G-25 > Dialysis.
常规信息
功能
Envelope glycoprotein gp160. Oligomerizes in the host endoplasmic reticulum into predominantly trimers. In a second time, gp160 transits in the host Golgi, where glycosylation is completed. The precursor is then proteolytically cleaved in the trans-Golgi and thereby activated by cellular furin or furin-like proteases to produce gp120 and gp41.. Surface protein gp120. Attaches the virus to the host lymphoid cell by binding to the primary receptor CD4. This interaction induces a structural rearrangement creating a high affinity binding site for a chemokine coreceptor like CXCR4 and/or CCR5. Acts as a ligand for CD209/DC-SIGN and CLEC4M/DC-SIGNR, which are respectively found on dendritic cells (DCs), and on endothelial cells of liver sinusoids and lymph node sinuses. These interactions allow capture of viral particles at mucosal surfaces by these cells and subsequent transmission to permissive cells. HIV subverts the migration properties of dendritic cells to gain access to CD4+ T-cells in lymph nodes. Virus transmission to permissive T-cells occurs either in trans (without DCs infection, through viral capture and transmission), or in cis (following DCs productive infection, through the usual CD4-gp120 interaction), thereby inducing a robust infection. In trans infection, bound virions remain infectious over days and it is proposed that they are not degraded, but protected in non-lysosomal acidic organelles within the DCs close to the cell membrane thus contributing to the viral infectious potential during DCs' migration from the periphery to the lymphoid tissues. On arrival at lymphoid tissues, intact virions recycle back to DCs' cell surface allowing virus transmission to CD4+ T-cells.. Transmembrane protein gp41. 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 fusion of viral and target intracellular membranes, the coiled coil regions (heptad repeats) 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. Complete fusion occurs in host cell endosomes and is dynamin-dependent, however some lipid transfer might occur at the plasma membrane. The virus undergoes clathrin-dependent internalization long before endosomal fusion, thus minimizing the surface exposure of conserved viral epitopes during fusion and reducing the efficacy of inhibitors targeting these epitopes. Membranes fusion leads to delivery of the nucleocapsid into the cytoplasm.
序列相似性
Belongs to the HIV-1 env protein family.
翻译后修饰
Highly glycosylated by host. The high number of glycan on the protein is reffered to as 'glycan shield' because it contributes to hide protein sequence from adaptive immune system.. Palmitoylation of the transmembrane protein and of Env polyprotein (prior to its proteolytic cleavage) is essential for their association with host cell membrane lipid rafts. Palmitoylation is therefore required for envelope trafficking to classical lipid rafts, but not for viral replication.. Specific enzymatic cleavages in vivo yield mature proteins. Envelope glycoproteins are synthesized as an inactive precursor that is heavily N-glycosylated and processed likely by host cell furin in the Golgi to yield the mature SU and TM proteins. The cleavage site between SU and TM requires the minimal sequence [KR]-X-[KR]-R. About 2 of the 9 disulfide bonds of gp41 are reduced by P4HB/PDI, following binding to CD4 receptor.
亚细胞定位
Host endosome membrane
靶点信息
其他靶点
Abcam Product Promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
For licensing inquiries, please contact partnerships@abcam.com