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首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >Peptide mimicry of the meningococcal group C capsular polysaccharide.
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Peptide mimicry of the meningococcal group C capsular polysaccharide.

机译:脑膜炎球菌C组荚膜多糖的肽模拟。

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摘要

Sequence analysis of the variable regions of the heavy and light chains of the anti-idiotypic antibody 6F9, which mimics the meningococcal group C capsular polysaccharide (MCP), was performed. The immunogenic site on 6F9 responsible for inducing an anti-MCP antibody response was determined by means of sequence and computer model analysis of these data. Complementarity-determining region 3 (CDR3) was found to be unique in that the sequence tract YRY was exposed on the surface. A synthetic peptide spanning the CDR3 domain was synthesized and complexed to proteosomes (meningococcal group B outer membrane protein). Immunizations of BALB/c mice with the peptide-proteosome complex resulted in a significant anti-MCP antibody response. Immunized mice were protected against infection with a lethal dose of Neisseria meningitidis serogroup C.
机译:对抗独特型抗体6F9的重链和轻链可变区进行了序列分析,该抗体模拟脑膜炎球菌C组荚膜多糖(MCP)。通过对这些数据的序列和计算机模型分析来确定负责诱导抗MCP抗体应答的6F9上的免疫原性位点。发现互补决定区3(CDR3)是独特的,因为序列YRY暴露在表面上。合成了跨越CDR3结构域的合成肽,并与蛋白体(脑膜炎球菌B组外膜蛋白)复合。用肽-蛋白体复合物免疫BALB / c小鼠导致明显的抗MCP抗体反应。用致死剂量的脑膜炎奈瑟氏球菌血清群C保护免疫小鼠免受感染。

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