Muro Y, Yamada T, Himeno M, Sugimoto K
Department of Dermatology, Nagoya University School of Medicine, Japan.
Clin Exp Immunol. 1998 Feb;111(2):372-6. doi: 10.1046/j.1365-2249.1998.00517.x.
Using autoimmune serum from a patient with anti-centromere antibodies, we have identified and partially characterized a novel protein with a mol. wt of approximately 27 kD (hereafter referred to as p27). A cDNA expression library was screened with this serum, and two overlapping inserts were isolated among three positive clones other than clones corresponding to centromere protein (CENP)-B and CENP-C. Analysis of the sequence showed an open reading frame of approximately 0.6 kb encoding 199 amino acids with a predicted mol. wt of 21.5 kD. Immunoblotting analysis with bacterial recombinant p27 showed that approximately 2% of anti-centromere antibody-positive patients had autoantibodies to p27, whereas only one of 215 autoimmune patients without anti-centromere antibodies reacted with the recombinant. All five cases with anti-p27 antibodies, who were diagnosed as having scleroderma and/or Sjögren's syndrome, showed internal organ involvement. Although affinity-purified anti-p27 human or mouse polyclonal antibodies failed to stain any cellular structures in an immunofluorescence study, the potential association of anti-p27 with anti-centromere antibodies suggests that this novel autoantigen might play a role in mitosis.
利用来自一名抗着丝粒抗体患者的自身免疫血清,我们鉴定并部分表征了一种分子量约为27 kD的新型蛋白质(以下简称p27)。用该血清筛选cDNA表达文库,除了对应着丝粒蛋白(CENP)-B和CENP-C的克隆外,在三个阳性克隆中分离出两个重叠插入片段。序列分析显示一个约0.6 kb的开放阅读框,编码199个氨基酸,预测分子量为21.5 kD。用细菌重组p27进行免疫印迹分析表明,约2%的抗着丝粒抗体阳性患者有针对p27的自身抗体,而215名无抗着丝粒抗体的自身免疫患者中只有1人对重组体有反应。所有五例抗p27抗体患者均被诊断为硬皮病和/或干燥综合征,均有内脏受累。尽管在免疫荧光研究中,亲和纯化的抗p27人或小鼠多克隆抗体未能对任何细胞结构进行染色,但抗p27与抗着丝粒抗体的潜在关联表明,这种新型自身抗原可能在有丝分裂中起作用。