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首页> 外文期刊>Protein engineering design & selection: PEDS >Rapid discovery and optimization of therapeutic antibodies against emerging infectious diseases.
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Rapid discovery and optimization of therapeutic antibodies against emerging infectious diseases.

机译:快速发现和优化针对新兴传染病的治疗性抗体。

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摘要

Using a comprehensive set of discovery and optimization tools, antibodies were produced with the ability to neutralize SARS coronavirus (SARS-CoV) infection in Vero E6 cells and in animal models. These anti-SARS antibodies were discovered using a novel DNA display method, which can identify new antibodies within days. Once neutralizing antibodies were identified, a comprehensive and effective means of converting the mouse sequences to human frameworks was accomplished using HuFR (human framework reassembly) technology. The best variant (61G4) from this screen showed a 3.5-4-fold improvement in neutralization of SARS-CoV infection in vitro. Finally, using a complete site-saturation mutagenesis methodology focused on the CDR (complementarity determining regions), a single point mutation (51E7) was identified that improved the 80% plaque reduction neutralization of the virus by greater than 8-fold. These discovery and evolution strategies can be applied to any emerging pathogen or toxin where a causative agent is known.
机译:使用一套全面的发现和优化工具,可以产生抗体,该抗体具有中和Vero E6细胞和动物模型中SARS冠状病毒(SARS-CoV)的能力。这些抗SARS抗体是使用新颖的DNA展示方法发现的,该方法可以在数天内识别出新抗体。鉴定出中和抗体后,即可使用HuFR(人类构架重组)技术完成将小鼠序列转化为人类构架的全面而有效的方法。此筛选的最佳变体(61G4)在体外的SARS-CoV感染中和中显示出3.5-4倍的改善。最后,使用针对CDR(互补决定区)的完整位点饱和诱变方法,鉴定出单点突变(51E7),可将病毒的80%噬菌斑减少中和性提高8倍以上。这些发现和进化策略可以应用于已知病原体的任何新兴病原体或毒素。

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