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Two common structural motifs for TCR recognition by staphylococcal enterotoxins

机译:葡萄球菌肠毒素识别TCR的两种常见结构基序

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Superantigens are toxins produced by Staphylococcus aureus, called staphylococcal enterotoxins (abbreviated SEA to SEU). They can cross-link the T cell receptor (TCR) and major histocompatibility complex class II, triggering a massive T cell activation and hence disease. Due to high stability and toxicity, superantigens are potential agents of bioterrorism. Hence, antagonists may not only be useful in the treatment of disease but also serve as countermeasures to biological warfare. Of particular interest are inhibitors against SEA and SEB. SEA is the main cause of food poisoning, while SEB is a common toxin manufactured as a biological weapon. Here, we present the crystal structures of SEA in complex with TCR and SEE in complex with the same TCR, complemented with computational alanine-scanning mutagenesis of SEA, SEB, SEC3, SEE, and SEH. We have identified two common areas that contribute to the general TCR binding for these superantigens. This paves the way for design of single antagonists directed towards multiple toxins.
机译:超抗原是金黄色葡萄球菌产生的毒素,称为葡萄球菌肠毒素(简称SEA到SEU)。它们可以使T细胞受体(TCR)与II类主要组织相容性复合物交联,从而引发大规模的T细胞活化,从而引发疾病。由于高度的稳定性和毒性,超抗原是生物恐怖主义的潜在诱因。因此,拮抗剂不仅可以用于治疗疾病,而且可以用作生物战的对策。特别令人感兴趣的是针对SEA和SEB的抑制剂。 SEA是食物中毒的主要原因,而SEB是作为生物武器生产的常见毒素。在这里,我们介绍了SEA与TCR配合使用的SEA晶体结构,以及与同一TCR配合的SEE的晶体结构,以及SEA,SEB,SEC3,SEE和SEH的计算丙氨酸扫描诱变。我们已经确定了两个共同的领域,这些领域有助于这些超抗原的一般TCR结合。这为设计针对多种毒素的单一拮抗剂铺平了道路。

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