Kieber-Emmons T, Kohler H
Proc Natl Acad Sci U S A. 1986 Apr;83(8):2521-5. doi: 10.1073/pnas.83.8.2521.
The question addressed in this report focuses on the autoantigenicity of self antigens, principally cytochrome c and lysozyme. Of interest is whether the immune system produces autoantibodies to its host proteins reacting randomly with all potential antigen sites or is autoreactively selective for certain determinants. Based on experimental evidence from autoantibodies against cytochromes c, Jemmerson and Margoliash [Jemmerson, R. & Margoliash, E. (1979) Nature (London) 282, 468-471] have described a striking correlation between autoreactive sequence regions and evolutionary instability. While their analysis of evolutionary variation was based on simple sequence variability plots, we present here a refined approach that takes into account the distinction between evolutionary substitutions that induce a change in the protein surface from those that do not (surface-neutral substitutions). A quantitative aspect of surface variation (surface consensus) is included in the algorithm that produces a ranked order for autoantigenic determinants. The final plot, called surface variability, indicates sequence regions having a preference for autoimmune reaction. We propose the term "autogen" to designate such protein determinants.
本报告所探讨的问题主要聚焦于自身抗原的自身抗原性,主要是细胞色素c和溶菌酶。令人感兴趣的是,免疫系统是会产生针对其宿主蛋白的自身抗体,与所有潜在抗原位点随机反应,还是会对某些决定簇进行自身反应性选择。基于针对细胞色素c的自身抗体的实验证据,杰默森和马戈利阿什[杰默森,R. & 马戈利阿什,E.(1979年)《自然》(伦敦)282卷,468 - 471页]描述了自身反应性序列区域与进化不稳定性之间的显著相关性。虽然他们对进化变异的分析基于简单的序列变异性图,但我们在此提出一种改进方法,该方法考虑了导致蛋白质表面发生变化的进化替代与未导致这种变化的替代(表面中性替代)之间的区别。算法中纳入了表面变异的定量方面(表面一致性),从而为自身抗原决定簇生成一个排序。最终的图称为表面变异性,它表明了倾向于自身免疫反应的序列区域。我们提出用“自身原”一词来指代此类蛋白质决定簇。