重组HIV1 p17 + p24 + gp120蛋白
Recombinant HIV1 p17 + p24 + gp120 protein
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Recombinant HIV1 p17 + p24 + gp120 protein is a Human immunodeficiency virus type 1 (NDK ISOLATE) Fragment protein, expressed in Escherichia coli, suitable for ELISA, WB.
查看别名
Envelope glycoprotein gp160, Env polyprotein, env
反应性数据
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
These proteins are fundamental in maintaining the structural integrity and infectivity of the HIV-1 virus. p17 ensures proper viral assembly and budding while p24 stabilizes the viral core both protecting the HIV-1 genome during replication. gp120 as part of the envelope protein complex with gp41 mediates entry of the virus by interacting with host cell receptors and co-receptors like CCR5 or CXCR4. This complex is important for the initial step in the viral replication cycle facilitating fusion of the viral and cellular membranes.
Pathways
HIV-1 p17 p24 and gp120 interact with multiple host cellular pathways during infection particularly those related to immune response and cell death. The gp120 protein engages the CD4+ T-cell signaling pathway leading to immune system evasion by the virus through T-cell depletion. These proteins are also involved in the apoptotic pathway where gp120 can induce apoptosis in uninfected cells via bystander effects contributing to the progression of AIDS. Other proteins like gp41 and viral protease are connected through these pathways supporting viral replication and pathogenesis.
特殊说明
形式
Liquid
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
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