Xie K, Snyder M
Department of Biology, Yale University, New Haven, CT 06520-8103.
Proc Natl Acad Sci U S A. 1995 Feb 28;92(5):1639-43. doi: 10.1073/pnas.92.5.1639.
To understand the relationship between antibodies present in patients with anti-nuclear dot (ND) autoimmune disease and the proteins they recognize, epitopes that react with the autoantibodies were mapped. A panel of fusion proteins containing different portions of the ND protein were overproduced in Escherichia coli. Immunoblot analysis with anti-ND antibodies revealed that most (10 of 12) sera recognize two major autoepitopes that are each a maximum of 8 amino acids long. The other two sera recognize one of the two epitopes. In addition to the short linear autoepitopes, a conformational epitope appears to be present on the ND antigen. Each of the two linear epitope sequences shares sequence similarities with those of several viral proteins found in the databases. Furthermore, two fusion proteins containing short Epstein-Barr virus (EBV) protein sequences that are similar to the ND epitopes were recognized by the human autoimmune sera, indicating that the autoepitopes are present in EBV protein sequences. Our results are consistent with the hypothesis that ND autoimmune disease might be associated with EBV infections.
为了解抗核点(ND)自身免疫病患者体内存在的抗体与其所识别的蛋白质之间的关系,绘制了与自身抗体发生反应的表位图谱。一组包含ND蛋白不同部分的融合蛋白在大肠杆菌中过量表达。用抗ND抗体进行免疫印迹分析表明,大多数(12份血清中的10份)血清识别两个主要自身表位,每个表位最长为8个氨基酸。另外两份血清识别其中一个表位。除了短线性自身表位外,ND抗原上似乎还存在一个构象表位。两个线性表位序列中的每一个都与数据库中发现的几种病毒蛋白的序列具有相似性。此外,两份含有与ND表位相似的短爱泼斯坦-巴尔病毒(EBV)蛋白序列的融合蛋白被人类自身免疫血清识别,这表明自身表位存在于EBV蛋白序列中。我们的结果与ND自身免疫病可能与EBV感染有关的假说一致。