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    • 1. 发明公开
    • A process for the preparation of a non-toxic anthrax vaccine
    • Herstellung einer nicht-toxischen Anthrax-Impfung的Verfahrenfür
    • EP1958960A2
    • 2008-08-20
    • EP08006580.8
    • 2002-03-20
    • Bhatnagar, Rakesh
    • The designation of the inventor has not yet been filed
    • C07K14/32C12N15/01
    • C07K14/32A61K39/00
    • Anthrax toxin, comprising of protective antigen (PA), lethal factor (LF) and edema factor (EF) is a major virulent factor of B. anthracis. Protective antigen, PA is the main component of all the vaccines against anthrax. The protective efficacy of PA is greatly increased if small quantities of LF or EF are incorporated into the vaccines. An ideal vaccine against anthrax should contain PA, LF and EF together, but this combination would be toxic. Therefore, the biologically inactive mutant preparations of PA, LF and EF may be used together for better immunoprotection. The present invention describes the method for generation of recombinant vaccine against anthrax, comprising of non-toxic, mutant anthrax toxin proteins. The procedure involves site-directed mutagenesis of the native genes of the toxin proteins, the expression and purification of the mutant proteins and finally characterization of these proteins.
    • 包含保护性抗原(PA),致死因子(LF)和水肿因子(EF)的炭疽毒素是炭疽杆菌的主要毒性因子。 保护性抗原,PA是所有针对炭疽疫苗的主要成分。 如果将少量的LF或EF并入疫苗中,则PA的保护功效大大增加。 一种针对炭疽的理想疫苗应包含PA,LF和EF,但这种组合是有毒的。 因此,PA,LF和EF的生物活性突变体制剂可以一起用于更好的免疫保护。 本发明描述了用于产生针对炭疽的重组疫苗的方法,其包含无毒的突变体炭疽毒素蛋白质。 该过程涉及毒素蛋白质的天然基因的定点突变,突变蛋白质的表达和纯化以及这些蛋白质的最终表征。