概述

描述

  • 性质Recombinant
  • 氨基酸序列
    • 种属Human
    • 额外的序列信息Selected from the Center region of human ERVWE1

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技术指标

Our Abpromise guarantee covers the use of ab91514 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

  • 应用

    Blocking - Blocking peptide for Anti-HERV antibody (ab71115)

  • 形式Liquid
  • Concentration information loading...

制备和贮存

  • 稳定性和存储

    Shipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid freeze / thaw cycles.

常规信息

  • 别名
    • Endogenous retrovirus group W member 1
    • env
    • Env-W
    • Envelope polyprotein gPr73
    • Enverin
    • ENW1_HUMAN
    • ERVW
    • ERVW-1
    • Gp24
    • Gp50
    • HERV-7q Envelope protein
    • HERV-W envelope protein
    • HERVW
    • SU
    • Syncytin
    • Syncytin 1
    • Syncytin-1
    • TM
    • Transmembrane protein
    see all
  • 功能Retroviral envelope proteins mediate receptor recognition and membrane fusion during early infection. Endogenous envelope proteins may have kept, lost or modified their original function during evolution. This endogenous envelope protein has retained its original fusogenic properties and participates in trophoblast fusion during placenta morphogenesis.
    SU mediates receptor recognition. This interaction triggers the refolding of the transmembrane protein (TM) and is thought to activate its fusogenic potential by unmasking its fusion peptide (By similarity). Seems to recognize the type D mammalian retrovirus receptors SLC1A4 and SLC1A5, as it induces fusion of cells expressing these receptors in vitro.
    The transmembrane protein (TM) 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 (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 membranes.
  • 组织特异性Expressed at higher level in placental syncytiotrophoblast. Expressed at intermediate level in testis. Seems also to be found at low level in adrenal tissue, bone marrow, breast, colon, kidney, ovary, prostate, skin, spleen, thymus, thyroid, brain and trachea. Both mRNA and protein levels are significantly increased in the brain of individuals with multiple sclerosis, particularly in astrocytes and microglia.
  • 序列相似性Belongs to the gamma type-C retroviral envelope protein family. HERV class-I W env subfamily.
  • 发展阶段In placenta, detected at higher level during early pregnancy and at lower level during late pregnancy.
  • 结构域The cytoplasmic region is essential for the fusiogenic function.
    The 17 amino acids long immunosuppressive region is present in many retroviral envelope proteins. Synthetic peptides derived from this relatively conserved sequence inhibit immune function in vitro and in vivo.
  • 翻译后修饰Specific enzymatic cleavages in vivo yield mature proteins. Envelope glycoproteins are synthesized as a inactive precursor that is heavily N-glycosylated and processed likely by 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. The intracytoplasmic tail cleavage by the viral protease that is required for the fusiogenic activity of some retroviruses envelope proteins seems to have been lost during evolution.
    The CXXC motif is highly conserved across a broad range of retroviral envelope proteins. It is thought to participate in the formation of a labile disulfide bond possibly with the CX6CC motif present in the transmembrane protein. Isomerization of the intersubunit disulfide bond to an SU intrachain disulfide bond is thought to occur upon receptor recognition in order to allow membrane fusion.
  • 细胞定位Cell membrane; Virion and Cell membrane. The surface protein is not anchored to the membrane, but localizes to the extracellular surface through its binding to TM.
  • Information by UniProt

HERV peptide (ab91514)参考文献

ab91514 has not yet been referenced specifically in any publications.

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