摘要
目的:分析人巨细胞病毒(HCMV)AD169株UL115基因序列,预测UL115基因编码的gL蛋白B细胞优势表位。方法:基于UL115基因编码的gL蛋白的氨基酸序列,结合亲水性参数、可及性参数、抗原性参数、柔韧性参数及二级结构方案对HCMVgL蛋白的B细胞表位进行预测,参照已建立的预测方法综合评价B细胞优势表位。结果:①UL115核酸变异集中在序列的N端,大部分是同义突变,氨基酸序列高度保守;②HC-MVgL蛋白B细胞表位可能位于编码蛋白N段197~205、253~261位。结论:多参数预测gL蛋白的B细胞优势表位,为进一步研究蛋白特征、制备单克隆抗体及表位疫苗提供依据。
Objective:To analyze the sequence of genome of cytomegalovirus UL115 and predict the B cell epitopes of the gL protein expressed by cytomegalovirus UL115.Method:The hydrophilicity,accessibility,antigenicity and flexibility index were used to predict the potential B cell epitopes of gL protein based on gL genome sequence.Result:① Most amino acid sequence of gL was highly conserved although several strains had variation.Those mutations focused on the N end of U115,but most of them were sense mutation.② The B cell epitopes of gL protein generated by combined application were predicted at gL protein N-terminal 197-205,253-261.Conclusion:The B-epitopes of gL protein was predicted successfully,which established the basis of the characterization of the protein,development of epitopes based vaccine,and preparation of monoclonal antibody against fusion protein.
出处
《临床血液学杂志(输血与检验)》
CAS
2012年第4期505-507,共3页
Journal of Clinical Hematology(Blood Transfusion & Laboratory Medicine)