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首页> 外文期刊>Journal of Immunological Methods >Plaque reduction test: an alternative method to assess specific antibody response to pIII-displayed peptide of filamentous phage M13.
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Plaque reduction test: an alternative method to assess specific antibody response to pIII-displayed peptide of filamentous phage M13.

机译:噬菌斑减少测试:一种评估对丝状噬菌体M13的pIII展示肽的特异性抗体反应的替代方法。

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Phage-displayed peptide systems have been used to identify the immunogenic epitopes and to develop the design of peptide-based or peptide-displaying phages themselves as vaccine candidates. To estimate the humoral immunity of phage-based vaccine, it is necessary to evaluate the antibody response specifically directed at the displayed peptide. Enzyme-linked immunosorbent assays (ELISAs) and Western blot analysis are commonly used for this purpose. However, using these methods, it is not easy to distinguish the antibody response against phage coat protein or the antibody response specific to the displayed peptide. The purified anti-Mycoplasma hyopneumoniae IgG was used to screen heptapeptides displaying on the pIII coat protein of M13 phage. Four selected phage clones were chosen to immunize mice. In order to evaluate the specific antibody response that is directed against heptapeptides, advantage was taken of the natural property of M13 phage to infect Escherichia coli, which is mediated by the pIII coat protein binding with the F pili of E. coli, and plaque reduction tests were performed to assess the specificity of antibody response. By comparing the number of plaques produced by the different phages (which are the same except for the displayed peptides) neutralized by the antiserum, we could demonstrate that the specificity of antibody response is directed against the peptide displayed on pIII coat protein. The results described here indicate that plaque reduction test is a convenient and more precise method to detect the antibody against the phage-displayed peptide.
机译:噬菌体展示的肽系统已经用于鉴定免疫原性表位,并开发了基于肽或展示肽的噬菌体本身作为候选疫苗的设计。为了评估基于噬菌体的疫苗的体液免疫性,有必要评估专门针对展示肽的抗体反应。为此目的通常使用酶联免疫吸附测定(ELISA)和Western印迹分析。然而,使用这些方法,不容易区分针对噬菌体外壳蛋白的抗体应答或对展示的肽特异的抗体应答。纯化的抗猪肺炎支原体IgG用于筛选在M13噬菌体的pIII外壳蛋白上展示的七肽。选择四个选择的噬菌体克隆以免疫小鼠。为了评估针对七肽的特异性抗体反应,利用了M13噬菌体感染大肠杆菌的天然特性,这是通过pIII外壳蛋白与大肠杆菌F菌毛结合和噬菌斑减少来介导的进行测试以评估抗体反应的特异性。通过比较由抗血清中和的不同噬菌体(除了展示的肽以外,相同的噬菌体)产生的噬菌斑数量,我们可以证明抗体反应的特异性针对pIII外壳蛋白上展示的肽。此处描述的结果表明,噬菌斑减少试验是检测针对噬菌体展示肽的抗体的便捷且更精确的方法。

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