• So, now you have a single molecule, very large molecule, with not just two binding sites but with ten binding sites.

    所以如果你体内有一个细胞,一个体积很大的细胞,细胞表面不只有两个抗原结合位点,而有十个抗原结合位点

    耶鲁公开课 - 生物医学工程探索课程节选

  • They might ingest extracellular antigen, presented pieces of it on their cell surface in the context of MHC-2.

    它们可以吞噬胞外抗原,根据细胞表面的,主要组织相容性抗原-2

    耶鲁公开课 - 生物医学工程探索课程节选

  • So, these are better at binding to antigen because they have more binding sites on them.

    连接抗体是对付抗原的有效方法,因为抗体表面将会有更多的抗原结合位点

    耶鲁公开课 - 生物医学工程探索课程节选

  • Then, your muscle cells would start producing Hepatitis B surface antigen and your immune system recognizing that's a foreign protein would start responding to it.

    于是,肌肉细胞将会,开始制造乙肝表面抗原,然后免疫系统就会识别出,那是外来蛋白质并且产生免疫应答

    耶鲁公开课 - 生物医学工程探索课程节选

  • Make a lot of the virus, it has all of its antigenic epitopes on it, but we'll just kill it so that it can't replicate.

    先增殖出大量的病毒,病毒表面有特定的抗原决定簇,然后杀死病毒使其无法复制

    耶鲁公开课 - 生物医学工程探索课程节选

  • Yeast cells were grown in large numbers with this plasmid inside, they expressed the plasmid and so you made Hepatitis B surface antigen not in people but in cell culture where it was not normally formed.

    体内携带这种质粒的酵母细胞大量增殖,它们表达质粒,因此,乙型肝炎表面抗原不是在人体内,而是在细胞培养环境下,以非正常方式形成的

    耶鲁公开课 - 生物医学工程探索课程节选

  • They also have binding sites for antigen, but they are sort of two IgG type molecules bound together by another peptide chain.

    同样IgA抗体表面也有与抗原结合位点,但它们就像两个IgG型分子,通过肽链相互连接

    耶鲁公开课 - 生物医学工程探索课程节选

  • These cells can now kill cells that have the correct signature, and the signature is MHC-1 with this foreign antigen associated with it.

    而这些细胞现在可以杀伤带标记的细胞,这些标记就是MHC-1表面受体,和与其相联的异己抗原

    耶鲁公开课 - 生物医学工程探索课程节选

  • We talked about host cells that are perhaps infected with a virus, displaying pieces of that virus, antigenic pieces of that virus in the context of a surface receptor called MHC-1, presenting that.

    我们说到过,可能受到病毒感染的宿主细胞,表现出病毒的一部分特征,病毒的抗原部分,其表面受体称为主要组织相容性抗原-1,MHC-1负责呈递抗原

    耶鲁公开课 - 生物医学工程探索课程节选

  • Well, one way to think about is they have more antigen binding sites and so they're going to be more efficient at neutralizing the pathogen on a per-molecule basis than IgG is.

    可以这么考虑,因为IgM表面有更多的抗原结合位点,所以相对于IgG,IgM在分子层面上,能够更为有效地与病原体结合

    耶鲁公开课 - 生物医学工程探索课程节选

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