{"title":"大肠杆菌l -天冬酰胺酶脱免疫的遗传算法","authors":"Raphael Trevizani","doi":"10.35259/isi.sact.2019_32695","DOIUrl":null,"url":null,"abstract":"Introduction: L-asparaginase is a heterologous enzyme expressed in Escherichia coli and used in leukemya therapy that triggers an immune response due to the presence of linear T-cell epitopes within the protein sequence. This results in the sustained production of antibodies that causes hypersensitivity problems and in the neutralization of the therapeutic effect. To diminish the potential immunogenicity, the protein can be subject to a process of epitope deletion via genetic manipulation of key MHC-high-binding residues. As an exhaustive evaluation of the mutants is prohibitive for experimental scientist because the number of variants is too big, in silico tools can be used to diminish the search space.","PeriodicalId":427855,"journal":{"name":"Anais do IV International Symposium on Immunobiological e VII Seminário Anual Científico e Tecnológico de Bio-Manguinhos","volume":"28 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Genetic algorithm for deimmunization of Escherichia coli L-asparaginase\",\"authors\":\"Raphael Trevizani\",\"doi\":\"10.35259/isi.sact.2019_32695\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Introduction: L-asparaginase is a heterologous enzyme expressed in Escherichia coli and used in leukemya therapy that triggers an immune response due to the presence of linear T-cell epitopes within the protein sequence. This results in the sustained production of antibodies that causes hypersensitivity problems and in the neutralization of the therapeutic effect. To diminish the potential immunogenicity, the protein can be subject to a process of epitope deletion via genetic manipulation of key MHC-high-binding residues. As an exhaustive evaluation of the mutants is prohibitive for experimental scientist because the number of variants is too big, in silico tools can be used to diminish the search space.\",\"PeriodicalId\":427855,\"journal\":{\"name\":\"Anais do IV International Symposium on Immunobiological e VII Seminário Anual Científico e Tecnológico de Bio-Manguinhos\",\"volume\":\"28 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1900-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Anais do IV International Symposium on Immunobiological e VII Seminário Anual Científico e Tecnológico de Bio-Manguinhos\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.35259/isi.sact.2019_32695\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Anais do IV International Symposium on Immunobiological e VII Seminário Anual Científico e Tecnológico de Bio-Manguinhos","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.35259/isi.sact.2019_32695","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
l -天门酰胺酶是一种在大肠杆菌中表达的异源酶,用于白血病治疗,由于在蛋白质序列中存在线性t细胞表位而引发免疫反应。这导致抗体的持续产生,导致过敏问题和治疗效果的中和。为了降低潜在的免疫原性,该蛋白可以通过对关键mhc高结合残基的遗传操作进行表位删除过程。由于突变体的数量太大,实验科学家无法对突变体进行详尽的评估,因此可以使用计算机工具来缩小搜索空间。
Genetic algorithm for deimmunization of Escherichia coli L-asparaginase
Introduction: L-asparaginase is a heterologous enzyme expressed in Escherichia coli and used in leukemya therapy that triggers an immune response due to the presence of linear T-cell epitopes within the protein sequence. This results in the sustained production of antibodies that causes hypersensitivity problems and in the neutralization of the therapeutic effect. To diminish the potential immunogenicity, the protein can be subject to a process of epitope deletion via genetic manipulation of key MHC-high-binding residues. As an exhaustive evaluation of the mutants is prohibitive for experimental scientist because the number of variants is too big, in silico tools can be used to diminish the search space.