| 冯燕,钟淑玲,徐昌平,卢亦愚.麻疹病毒血凝素蛋白抗原表位的预测与分析[J].Chinese journal of Epidemiology,2015,36(9):983-987 |
| 麻疹病毒血凝素蛋白抗原表位的预测与分析 |
| Prediction and analysis of epitopes of hemagglutinin of measles virus |
| Received:January 30, 2015 |
| DOI：10.3760/cma.j.issn.0254-6450.2015.09.016 |
| KeyWord: 麻疹病毒 血凝素蛋白 抗原表位 多肽 抗原特异性 |
| English Key Word: Measles virus Hemagglutinin Epitope Peptide Antigenic specificity |
| FundProject:浙江省医学重点学科群(XKQ-009-003) |
| Author Name | Affiliation | E-mail | | Feng Yan | Key Laboratory of Emergency Detection for Public Health of Zhejiang Province, Zhejiang Provincial Center for Disease Control and Prevention, Hangzhou 310051, China | | | Zhong Shuling | Key Laboratory of Emergency Detection for Public Health of Zhejiang Province, Zhejiang Provincial Center for Disease Control and Prevention, Hangzhou 310051, China | | | Xu Changping | Key Laboratory of Emergency Detection for Public Health of Zhejiang Province, Zhejiang Provincial Center for Disease Control and Prevention, Hangzhou 310051, China | | | Lu Yiyu | Key Laboratory of Emergency Detection for Public Health of Zhejiang Province, Zhejiang Provincial Center for Disease Control and Prevention, Hangzhou 310051, China | luyiyuzjh@163.com |
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| Abstract: |
| 目的 探讨麻疹病毒(MeV)流行株血凝素蛋白(H)抗原表位上氨基酸(aa)变异对病毒抗原性的可能影响。方法 利用生物信息学软件预测MeV H蛋白上B细胞线性表位,设计并合成来源于疫苗株和流行株表位以及同一区域非表位上的多肽对。间接ELISA法检测合成多肽的免疫原性,并制备多肽免疫血清。采用交叉ELISA法分析两条多肽间的抗原性差异,计算抗原比。结果 合成的多肽均能与MeV免疫血清结合,其中设计在表位区的多肽对CW23/CW22(273～282 aa)结合能力最强,而非表位区多肽对CW150/CW151(418～427 aa)结合能力最弱。多肽对中来源不同两条多肽间抗原性差异较大,其中CW23(疫苗株来源)与CW22(流行株来源)间抗原比为16,CW123(疫苗株来源)与CW124(流行株来源)(236～246 aa)间的抗原比为2.877±0.583。非表位多肽对中,CW125与CW126(356～364 aa)间抗原比为1.631±0.481,而CW150与CW151间抗原比为10.367±1.617。结论 麻疹流行株上仍存在保守的抗原表位,但预测的抗原表位及非表位区上的部分aa变异导致疫苗株与流行株间抗原性存在差异。 |
| English Abstract: |
| Objective To discuss the antigenic change caused by the mutation of amino acid on the epitopes of the hemagglutinin of measles virus. Methods The B cell linear epitopes in the hemagglutinin were predicted with bioinformatics software. Peptide pairs,which located on the same region but originated from measles vaccine and wild-type virus respectively,were designed and synthesized. After detecting the immunogenicity of peptides with indirect ELISA assay,sera against each peptide was prepared. Antigenic specificity between the two peptides within each peptide pair were tested by using cross ELISA assay,and then antigen ratios were calculated. Results All the synthesized peptides could bind with immune sera against measles virus,of which the peptide pair CW23/CW22 designed on the epitope region (273-282 aa) possessed the highest binding ability,while the peptide pair CW150/CW151 designed on the non-epitope region (418-427 aa) showed the lowest binding ability. The difference in antigenic specificity between the two peptides from different sources was significant. The antigenic ratio was up to 16 between CW23 (vaccine-originated) and CW22 (wild-type originated),and 2.877±0.583 between CW123 (vaccine-originated) and CW124 (wild-type originated)(236-246 aa). On the non-epitope regions,the antigenic ratios was only 1.631±0.481 between peptide pair CW125 and CW126(356-364 aa),but reached to 10.367±1.617 between CW150 and CW151. Conclusion Although there were several conservative epitopes,specific amino acid mutation on the predicted epitope or non-epitope regions might cause the antigenic change of wild-type measles virus. |
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