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Epitope-Cavities Generated by Molecularly Imprinted Films Measure the Coincident Response to Anthrax Protective Antigen and Its Segments

机译:分子印迹膜产生的抗原决定簇腔测量对炭疽保护性抗原及其节段的重合反应。

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摘要

A molecularly imprinted film was fabricated, in the presencenof epitope-peptides, onto a quartz crystal microbalancen(QCM) chip. These five peptides are known linearnor conformational epitopes of the anthrax protectivenantigen PA83. Imprinting resulted in an epitope-cavitynwith affinity for the corresponding template. With thenuse of a basic monomer, the binding-effect was furthernenhanced increasing the affinity to nanomolar levels.nThe affinities of the peptide to their correspondingnmolecularly induced polymers (MIPs) were morenclosely related to the molecular weight of the analytenthan to the number of residues. All epitope-cavitiesndifferentiated their epitope region on the protectivenantigen PA83 as well as the corresponding furin cleavagenfragments PA63 and PA20. The QCM chip differentialnresponse to the protective antigen fragmentnwas observed in the picomolar range, thus demonstratingna method to manipulate protein on the surfacenwith defined orientation.
机译:在存在表位肽的情况下,将分子印迹膜制备到石英晶体微天平(QCM)芯片上。这五个肽是炭疽保护性抗原PA83的线性或构象表位。印迹导致对相应模板的表位-cavitynwith亲和力。然后使用碱性单体,进一步增强了结合效果,从而增加了与纳摩尔水平的亲和力。n肽与相应分子诱导的聚合物(MIP)的亲和力与被分析物的分子量更密切相关,而与残基数量无关。所有的表位腔都在保护性抗原PA83以及相应的弗林蛋白酶切割原片段PA63和PA20上分化了其表位区域。在皮摩尔范围内观察到了QCM芯片对保护性抗原片段的差异反应,从而证明了一种以规定的方向操纵表面蛋白的方法。

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