Urbanski G J, Margoliash E
J Immunol. 1977 Apr;118(4):1170-80.
Rabbit, mouse, and guanaco cytochromes c differ from each other by only two amino acid residues. The identification is described of all of the antigenic determinants of mouse and guanaco cytochrome c that elicit an antibody response in rabbits, and those of the rabbit and guanaco proteins that elicity antibodies in the mouse. All except one of these sites center around single amino acid residue differences between the antigen and the host cytochrome c. The corresponding antibody popylations bind only to the areas of the protein in which the substitutions occur. Such antigenic determinants manifested in rabbits by quanaco and mouse cytochromes c are centered around residues 62 and 89, and residues 44 and 89, respectively. Similarly, the mouse recognizes sites containing residues 44 and 62 in guanaco cytochrome c, and residues 44 and 89 in rabbit cytochrome c. In none of these instances has a change in sequence failed to produce an antibody response. Each of these determinants appears to elicit and bind to its antibody, independently of other determinants present on the protein. In addition, two different autoantigenic responses have been detected. The antibodies produced against the determinant formed by glutamyl residue 62 of the guanaco protein in both rabbits and mice, the cytochromes c of which carry an aspartyl residue in that position, also bind to the aspartyl-containing region but with lower affinity. However, mouse and rabbit cytochrome c also elicit antibodies to the area of residue 62 in rabbits and mice, respectively, and these antibodies still bind more strongly to the glutamyl-than to the aspartyl-containing determinant. This last response occurs only when there are residue substitutions elsewhere in the molecule, because mice and rabbits fail to respond to their own cytochrome c. Antibodies produced in mice against the change from alanyl to valyl residue 44 by rabbit and guanaco cytochromes c also bind to the alanyl-containing determinant, except less tightly than to the valyl region. Conversely, antibodies raised in rabbits against the change from valyl to alanyl residue 44 only bind to this region when it carries an alanine. It is suggested that antigenic determinants that arise as a result of amino acid residue substitutions between the immunizing and the corresponding host protein, without a change in the spatial arrangement of the polypeptide backbone, be termed topographic determinants.
兔、小鼠和原驼的细胞色素c彼此之间仅相差两个氨基酸残基。本文描述了小鼠和原驼细胞色素c中所有能在兔体内引发抗体反应的抗原决定簇,以及兔和原驼蛋白中能在小鼠体内引发抗体反应的抗原决定簇。除了一个位点外,所有这些位点都围绕着抗原与宿主细胞色素c之间的单个氨基酸残基差异。相应的抗体群体仅与蛋白质中发生替换的区域结合。原驼和小鼠细胞色素c在兔体内表现出的此类抗原决定簇分别围绕第62和89位残基,以及第44和89位残基。同样,小鼠识别原驼细胞色素c中包含第44和62位残基的位点,以及兔细胞色素c中包含第44和89位残基的位点。在这些情况中,序列的改变无一未能产生抗体反应。这些决定簇中的每一个似乎都能独立于蛋白质上存在的其他决定簇引发并结合其抗体。此外,还检测到了两种不同的自身抗原反应。在兔和小鼠体内针对原驼蛋白第62位谷氨酰残基形成的决定簇产生的抗体,其细胞色素c在该位置携带天冬氨酰残基,也能结合含天冬氨酰的区域,但亲和力较低。然而,小鼠和兔的细胞色素c也分别在兔和小鼠体内引发针对第62位残基区域的抗体,并且这些抗体与含谷氨酰的决定簇的结合仍然比与含天冬氨酰的决定簇的结合更强。最后这种反应仅在分子其他部位存在残基替换时才会发生,因为小鼠和兔对自身的细胞色素c没有反应。小鼠体内针对兔和原驼细胞色素c将第44位丙氨酰残基变为缬氨酰残基而产生的抗体,也能结合含丙氨酰的决定簇,但结合程度不如与含缬氨酰区域的结合紧密。相反,兔体内针对第44位缬氨酰残基变为丙氨酰残基而产生的抗体,只有当该区域携带丙氨酸时才会结合该区域。有人提出,由于免疫蛋白与相应宿主蛋白之间氨基酸残基替换而产生的抗原决定簇,在多肽主链的空间排列没有改变的情况下,应称为拓扑决定簇。