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一个主要由碱性氨基酸组成的带电荷片段形成了着丝粒蛋白A的自身表位。

A charged segment mainly composed of basic amino acids forms an autoepitope of CENP-A.

作者信息

Muro Y, Iwai T, Ohashi M

机构信息

Department of Dermatology, Nagoya University School of Medicine, Japan.

出版信息

Clin Immunol Immunopathol. 1996 Jan;78(1):86-9. doi: 10.1006/clin.1996.0013.

DOI:10.1006/clin.1996.0013
PMID:8599890
Abstract

Autoantibodies against centromere proteins are commonly found in the serum of patients with scleroderma and other systemic autoimmune diseases. The reactivity of anticentromere autoantibodies (ACA) from 78 patients was investigated by ELISA using two kinds of a 15-amino-acid peptide corresponding to the N- and C-termini of CENP-A, one of the target molecules of ACA. The N-terminal peptide (residues 3-17) was recognized by 85% of ACA, while the C- terminal peptide (residues 126-140) was not. The ELISA result for the N-terminal peptide correlated with the immunoreactivity of CENP-A observed in immunoblotting. Moreover, the binding between autoantibodies and CENP-A was inhibited by the N-terminal peptide in 98.5% of anti-CENP-A- positive sera in immunoblotting. The sequence of peptide, PRRRSRKPEAPRRRS, is highly charged and has two repeats of PRRRS. These results indicate that the N-terminal-charged region forms a major epitope of CENP-A. This area may be involved in the induction of specific autoantibodies against centromere in autoimmune patients.

摘要

抗着丝粒蛋白自身抗体常见于硬皮病和其他系统性自身免疫性疾病患者的血清中。采用酶联免疫吸附测定(ELISA)法,使用两种分别对应于抗着丝粒自身抗体(ACA)的一种靶分子CENP - A的N端和C端的15个氨基酸的肽段,对78例患者的抗着丝粒自身抗体(ACA)的反应性进行了研究。85%的ACA能识别N端肽段(第3 - 17位氨基酸残基),而C端肽段(第126 - 140位氨基酸残基)则不能被识别。N端肽段的ELISA结果与免疫印迹中观察到的CENP - A的免疫反应性相关。此外,在免疫印迹中,98.5%的抗CENP - A阳性血清中的自身抗体与CENP - A之间的结合被N端肽段所抑制。肽段序列PRRRSRKPEAPRRRS带电量高,且有两个PRRRS重复序列。这些结果表明,N端带电区域构成了CENP - A的主要表位。该区域可能参与了自身免疫患者中抗着丝粒特异性自身抗体的诱导过程。

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A charged segment mainly composed of basic amino acids forms an autoepitope of CENP-A.一个主要由碱性氨基酸组成的带电荷片段形成了着丝粒蛋白A的自身表位。
Clin Immunol Immunopathol. 1996 Jan;78(1):86-9. doi: 10.1006/clin.1996.0013.
2
Autoepitopes on autoantigen centromere protein-A (CENP-A) are restricted to the N-terminal region, which has no homology with histone H3.自身抗原着丝粒蛋白A(CENP-A)上的自身表位局限于N端区域,该区域与组蛋白H3没有同源性。
Clin Exp Immunol. 2000 Apr;120(1):218-23. doi: 10.1046/j.1365-2249.2000.01189.x.
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The clinical expression in anticentromere antibody-positive patients is not specified by the epitope recognition of CENP-B antigen.抗着丝粒抗体阳性患者的临床表型并非由CENP - B抗原的表位识别所决定。
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Detection of anticentromere antibodies using recombinant human CENP-A protein.使用重组人着丝粒蛋白A(CENP-A)检测抗着丝粒抗体
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引用本文的文献

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Fine specificity mapping of autoantigens targeted by anti-centromere autoantibodies.抗着丝粒自身抗体靶向的自身抗原的精细特异性图谱分析。
J Autoimmun. 2006 Dec;27(4):272-80. doi: 10.1016/j.jaut.2006.10.001. Epub 2007 Jan 8.
3
Autoepitopes on autoantigen centromere protein-A (CENP-A) are restricted to the N-terminal region, which has no homology with histone H3.
自身抗原着丝粒蛋白A(CENP-A)上的自身表位局限于N端区域,该区域与组蛋白H3没有同源性。
Clin Exp Immunol. 2000 Apr;120(1):218-23. doi: 10.1046/j.1365-2249.2000.01189.x.