[Prediction and Identification of Immunodominant Linear B Cell Epitopes in the Nucleocapsid Protein of SFTSV].

Jun Chen, Peibei Sun, Feng Zhang, Chunyan Gu, Meng Gao, Hongxia Ni, Yongneng Luo
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Abstract

In order to identify immunodominant linear B cell epitopes in the nucleocapsid protein N of severe fever with thrombocytopenia syndrome virus(SFTSV),bioinformatics programs were used to analyze antigenicity, hydrophilicity and surface probability of the amino acid sequence and predict possible linear B cell epitopes. PyMOL software was used to analyze the distribution of linear B cell epitopes in nucleocapsid protein N based on its crystal structure. Corresponding peptides were synthesized and examined in peptide enzyme-linked immunosorbent assay(Peptide-ELISA)individually to check whether they reacted with sera from SFTSV-infected patients. As a result, a total of six potential linear B cell epitopes were predicted as the following: A(40-KKLKETGGDDWVKDTK-55), B(71-ASGKMSNSGSKRL-83), C(94-ERAETRL-100),D(135-LKVENYPP-142),E(157-GVSEATT-163)and F(184-KMRGASKTEVYNSFRDP-200).All epitopes were located on the surface of the nucleocapsid protein N and contained flexible loops. Each of the six synthetic peptides reacted positively with sera from SFTSV-infected patients and were identified as immunodominant linear B cell epitopes. Linear regression analysis showed a positive correlation between each peptide-ELISA and commercialized N protein-based EIA. In this study, immunodominant linear B cell epitopes from the nucleocapsid protein N of SFTSV were successfully predicted and confirmed. These findings may help to establish the molecule basis of specific antigenicity and disease diagnosis.

[SFTSV核衣壳蛋白免疫显性线性B细胞表位的预测和鉴定]。
为了鉴定发热伴血小板减少综合征病毒(SFTSV)核衣壳蛋白N的免疫显性线性B细胞表位,采用生物信息学方法分析其氨基酸序列的抗原性、亲水性和表面概率,并预测可能的线性B细胞表位。利用PyMOL软件根据核衣壳蛋白N的晶体结构,分析线性B细胞表位在核衣壳蛋白N中的分布。合成相应的肽段,分别用肽酶联免疫吸附试验(peptide - elisa)检测其是否与sftsv感染者血清发生反应。结果,共预测了6个潜在的线性B细胞表位:a (40-KKLKETGGDDWVKDTK-55)、B(71-ASGKMSNSGSKRL-83)、C(94-ERAETRL-100)、D(135-LKVENYPP-142)、E(157- gvseat -163)和F(184-KMRGASKTEVYNSFRDP-200)。所有的表位都位于核衣壳蛋白N的表面,并含有柔性环。6种合成肽均与sftsv感染患者血清反应阳性,并被鉴定为免疫优势线性B细胞表位。线性回归分析显示,各肽段- elisa与商品化N蛋白EIA呈正相关。本研究成功预测并确认了SFTSV核衣壳蛋白N的免疫优势线性B细胞表位。这些发现可能有助于建立特异性抗原性和疾病诊断的分子基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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