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Genome-Based Bioinformatic Selection of Chromosomal Bacillus anthracis Putative Vaccine Candidates Coupled with Proteomic Identification of Surface-Associated Antigens

机译:基于基因组的炭疽芽孢杆菌推定疫苗候选者的生物信息学选择,再结合蛋白质组学鉴定表面相关抗原

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Bacillus anthracis (Ames strain) chromosome-derived open reading frames (ORFs), predicted to code for surface exposed or virulence related proteins, were selected as B. anthracis-specific vaccine candidates by a multistep computational screen of the entire draft chromosome sequence (February 2001 version, 460 contigs, The Institute for Genomic Research, Rockville, Md.). The selection procedure combined preliminary annotation (sequence similarity searches and domain assignments), prediction of cellular localization, taxonomical and functional screen and additional filtering criteria (size, number of paralogs). The reductive strategy, combined with manual curation, resulted in selection of 240 candidate ORFs encoding proteins with putative known function, as well as 280 proteins of unknown function. Proteomic analysis of two-dimensional gels of a B. anthracis membrane fraction, verified the expression of some gene products. Matrix-assisted laser desorption ionization-time-of-flight mass spectrometry analyses allowed identification of 38 spots cross-reacting with sera from B. anthracis immunized animals. These spots were found to represent eight in vivo immunogens, comprising of EA1, Sap, and 6 proteins whose expression and immunogenicity was not reported before. Five of these 8 immunogens were preselected by the bioinformatic analysis (EA1, Sap, 2 novel SLH proteins and peroxiredoxin/AhpC), as vaccine candidates. This study demonstrates that a combination of the bioinformatic and proteomic strategies may be useful in promoting the development of next generation anthrax vaccine.
机译:选择 Bacillus anthracis (Ames菌株)染色体衍生的开放阅读框(ORF),将其编码为表面暴露或毒力相关蛋白的编码,被选为 B。通过整个染色体序列初稿的多步计算筛选(2001年2月版,460个重叠群,基因组研究所,马里兰州罗克维尔),选择特定的炭疽疫苗。选择程序结合了初步注释(序列相似性搜索和域分配),细胞定位预测,分类学和功能筛选以及其他过滤标准(大小,旁系同源物数量)。还原策略,与手动策展相结合,导致选择了240个候选ORF,这些ORF编码具有已知功能的蛋白质以及280种功能未知的蛋白质。蛋白质B的二维凝胶的蛋白质组学分析。炭疽膜部分,证实了某些基因产物的表达。基质辅助激光解吸电离飞行时间质谱分析可以鉴定与 B血清发生交叉反应的38个斑点。炭疽疫苗免疫的动物。发现这些斑点代表八个体内免疫原,包括EA1,Sap和6种蛋白质,这些蛋白质的表达和免疫原性以前没有报道。通过生物信息学分析预先选择了这8种免疫原中的5种(EA1,Sap,2种新型SLH蛋白和过氧化物酶/ AhpC)作为候选疫苗。这项研究表明,生物信息学和蛋白质组学策略的结合可能有助于促进下一代炭疽疫苗的开发。

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