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During most eukaryotic translation processes, the small 40S ribosome subunit scans an mRNA from its 5' end until it encounters the first start AUG codon. The large 60S ribosomal subunit then joins the smaller one to initiate protein synthesis. The location of the translation initiation is largely determined by the nucleotides near the start codon as there may be multiple translation initiation sites present on the mRNA.  Marilyn Kozak discovered that the sequence RCCAUGG (where R...
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Receptor-mediated endocytosis is when bulk amounts of specific molecules are imported into a cell after binding to cell surface receptors. The molecules bound to these receptors are taken into the cell through inward folding of the cell surface membrane, which is eventually pinched off into a vesicle within the cell. Structural proteins, such as clathrin, coat the budding vesicle.
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Multivesicular bodies (MVBs) are mature endosomes that sort ubiquitinated proteins and then fuse with lysosomes to degrade the sorted proteins. Epidermal growth factor (EGF) and its receptor (EGFR) form a complex that can be internalized through endocytosis, sorted into an MVB, and later degraded.
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通过疹病毒诱受体对化学基因封存的结构基础

Jennifer M Alexander1, Christopher A Nelson, Victor van Berkel

  • 1Department of Pathology and Immunology, Washington University School of Medicine, 660 South Euclid Avenue, St. Louis, MO 63110, USA.

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鼠性马疹病毒68 (gamma HV68) M3蛋白通过结合化学吸引剂细胞因子来破坏免疫系统. 晶体结构揭示了M3的存在.

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科学领域:

  • 结构生物学是结构生物学.
  • 病毒学 病毒学
  • 免疫学 免疫学 免疫学

背景情况:

  • 鼠玛疹病毒68 (玛HV68) M3蛋白是一种免疫调节器.
  • M3蛋白通过激活化学吸引细胞因子,干扰宿主抗病毒炎症反应.

研究的目的:

  • 阐明M3蛋白与化学因子相互作用的结构基础.
  • 了解M3蛋白如何调节宿主免疫反应.

主要方法:

  • 采用X射线晶体学,单独确定M3蛋白的结构,并与MCP-1复合确定M3蛋白的结构.
  • 结构分析的重点是M3蛋白的域架构,二元化和化学激素结合接口.

主要成果:

  • 晶体结构显示M3蛋白是一种两域β三明治蛋白,形成一个反平行二元体.
  • M3-MCP-1复合体表现出2:2的固体几何学,其中化学基因与二分体的远端结合在一起.
  • M3蛋白利用形状灵活性和静电互补性来实现高亲和度,广泛的化学基因结合,并采用结构模仿.

结论:

  • M3 蛋白质的独特结构有助于散乱的化学结合,模仿与化学受体的相互作用.
  • 这些发现提供了对病毒免疫逃避策略和潜在治疗点的见解.