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严重急性呼吸综合征冠状病毒核衣壳蛋白上抗原位点的定位

Mapping of antigenic sites on the nucleocapsid protein of the severe acute respiratory syndrome coronavirus.

作者信息

He Yuxian, Zhou Yusen, Wu Hao, Kou Zhihua, Liu Shuwen, Jiang Shibo

机构信息

Lindsley F. Kimball Research Institute, New York Blood Center, New York, NY 10021, USA.

出版信息

J Clin Microbiol. 2004 Nov;42(11):5309-14. doi: 10.1128/JCM.42.11.5309-5314.2004.

Abstract

Antigenic sites on the nucleocapsid (N) protein of severe acute respiratory syndrome (SARS) coronavirus (SARS-CoV) were mapped by Pepscan analysis with overlapping peptides that span the N protein sequence. Two major immunodominant epitopes located in the C-terminal region (amino acids [aa] 362 to 412) and middle region (aa 153 to 178) reacted with more than 75% of sera from SARS patients. Several minor immunodominant epitopes were reactive with about 50% of the SARS sera. Antisera from mice immunized with inactivated SARS-CoV recognized the two major immunodominant epitopes and one antigenic site located adjacent to the N-terminal region (aa 76 to 101), which did not react with the sera from SARS patients. Several monoclonal antibodies against SARS-CoV bound to the N- or C-terminal antigenic sites. These results suggest that the above antigenic sites on the N protein are important in eliciting humoral immune response against SARS-CoV in humans and animals and can be used as antigens for developing diagnostic tests.

摘要

通过用跨越核衣壳(N)蛋白序列的重叠肽进行Pepscan分析,绘制了严重急性呼吸综合征(SARS)冠状病毒(SARS-CoV)N蛋白上的抗原位点。位于C末端区域(氨基酸[aa]362至412)和中间区域(aa 153至178)的两个主要免疫显性表位与超过75%的SARS患者血清发生反应。几个次要免疫显性表位与约50%的SARS血清发生反应。用灭活的SARS-CoV免疫的小鼠抗血清识别两个主要免疫显性表位和一个位于N末端区域附近(aa 76至101)的抗原位点,该位点不与SARS患者的血清发生反应。几种抗SARS-CoV单克隆抗体与N或C末端抗原位点结合。这些结果表明,N蛋白上的上述抗原位点在引发人和动物针对SARS-CoV的体液免疫反应中很重要,可作为开发诊断测试的抗原。

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