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首页> 外文期刊>Biotechnology Progress >An Improved Phage Display Procedure for Identification of Lipopolysaccharide-Binding Peptides
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An Improved Phage Display Procedure for Identification of Lipopolysaccharide-Binding Peptides

机译:一种改进的噬菌体展示程序,用于鉴定脂多糖结合肽

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摘要

We successfully implemented several modifications to the regular phage display procedure and significantly improved the lipopolysaccharides-binding properties of the peptides selected.Specifically,the number of biopannings was increased and peptides with consensus sequences were obtained.A dual selection procedure (referred to as subtractive panning) was used to simultaneously select for the desired target and deselect for an undesired target,thereby increasing the binding specificity.In addition,binding and washing conditions in the subtractive panning were also modified to favor the selection of peptides with higher binding strength.As a result,two peptides,ASFPPAF and SSHTISF,were identified with much improved binding properties compared to those selected with regular panning.The binding specificities of these two peptides,as measured by the ratio of phages bound to the desired and undesired targets,were severalfold higher than previously reported.These modifications could easily be implemented with many other target molecules,indicating the general applicability of the procedure.
机译:我们成功地对常规噬菌体展示程序进行了几处修改,并显着改善了所选肽的脂多糖结合特性。特别是,增加了生物淘选的数量并获得了具有共有序列的肽。双重选择程序(称为减性淘选) )用于同时选择所需的靶标和取消选择不需要的靶标,从而提高结合特异性。此外,还对减数淘选中的结合和洗涤条件进行了修改,以利于选择具有更高结合强度的肽。结果,与常规淘选相比,鉴定出两种肽,ASFPPAF和SSHTISF,其结合性能大大提高。这两种肽的结合特异性,是通过噬菌体与所需靶标和不需要靶标结合的比率测得的比以前报道的这些修改很容易与许多其他靶分子结合使用,表明该方法的一般适用性。

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