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生物信息学预测小鼠转铁蛋白受体B细胞表位 被引量:1

Prediction of B-cell epitope of transferrin receptor using bioinformatical Methods
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摘要 目的:预测小鼠转铁蛋白受体(transferrin receptor, TfR)的B细胞表位,为构建以TfR抗体为脑转运载体的疫苗提供基础。方法:以小鼠转铁蛋白受体基因序列为基础,按Chou-Fasman和Gamier-Robson方法预测其编码蛋白的二级结构,按Kyte-Doolittle方法预测其亲水性,Emini方法预测其表面可能性以及按Jameson-Wolf方法预测其抗原指数。结果:Chou-Fasman和Gamier-Robson方法发现90 - 110, 120 - 145, 160 - 180, 240 - 250, 265 - 275, 290 - 304, 336 - 350, 375 - 383, 426 - 435, 504 - 517, 590 - 602, 613 - 630, 710 - 718这些区域可能为α螺旋的中心区域。用Kyte-Doolittle、 Emini、 Jameson-Wolf方法分别对小鼠TfR的B细胞表位进行预测,结果显示其共有区域为30 - 50, 100 - 115, 145 - 157, 310 - 320, 355 - 360, 440 - 445, 510 - 535, 655 - 660, 690 - 695, 705 - 710。根据抗原表位设计原则筛选出5段符合要求的抗原表位氨基酸序列:DGDNSH, AETEETDKS,NTYTP,MDKNKF,KHPVDGKSLYRDSNWISKV,它们可能为小鼠转铁蛋白受体的B细胞优势表位区域。结论:该结果有助于确定小鼠转铁蛋白受体的B细胞表位以及构建药物-载体复合物,发挥其脑药物转运载体的功能。 Objective: To predict the B-cell epitope of transferrin receptor, for providing a foundation of constructing a vaccine carried by transferrin receptor antibody through the blood-brain barrier. Methods: The secondary structure and hydrophilicity plot were extrapolated using Chou-Fasman, Gamier-Robson and Kyte-Doolittle methods based on the genetic sequence of transferrin receptor. Surface probability plot and antigenic index of transferrin receptor were predicted using the Emini and Jameson-Wolf methods respectively. Results: Centers of α-helix were found in the regions of 90 - 110, 120 - 145, 160 - 180, 240 - 250, 265 - 275, 290 - 304, 336 - 350, 375 - 383, 426 - 435, 504 - 517, 590 - 602, 613 - 630, 710 - 718. B-cell epitope of transferrinreceptor were possibly localized in the regions of 30 - 50, 100 - 115, 145 - 157, 310 - 320, 355 - 360, 440 - 445, 510 - 535, 655 - 660, 690 - 695, 705 - 710. Based on the design principle of antigen epitopes, five sections of amino acid sequence were screaned out which accorded with the requirements: DGDNSH, AETEETDKS, NTYTP, MDKNKF, KHPVDGKSLYRDSNWISKV.These sections may be the potential B - cell epitope region of mouse transferrin receptor. Conclusion: These results are helpful for identifying the dominant B-cell epitope and constructing the drug-carrier compound as a brain drug carrier.
出处 《泸州医学院学报》 2013年第6期580-584,共5页 Journal of Luzhou Medical College
基金 四川省教育厅重点项目(2006A055)
关键词 生物信息学 转铁蛋白受体 B细胞表位 Bioimformatics Transferrin receptor B-cell epitope
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