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Novel High-affinity Aβ-binding peptides identified by an advanced in vitro evolution, progressive library method

机译:通过先进的体外进化,渐进文库方法鉴定出新型高亲和力Aβ结合肽

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Recent studies have been supporting that the generation of Aβ42 oligomers is responsible for Alzheimer's disease. Therefore, those peptides which bind to Aβ42 are Sci.entifically interesting and can be possible candidates for the diagnosis and therapy of Alzheimer's disease. A systemic in vitro evolution, developed recently and the designated progressive library method (PLM), was applied to obtain Aβ42-binding aptamers Peptides As a result, high affinity peptide aptamers made of 8 or 9 amino acids could be identified by this approach, endorsing the methodological effectiveness. Namely, the selection products from the secondary library of diversified peptides, which was constructed based on the information obtained from the primary library selection, were confirmed to be superior to those selected from the primary library as had been reported previously. The affinities of those peptides measured by SPR (surface plasmon resonance) were comparable to or higher than that of those peptides so far reported (Kd of 10-7). The other peptides selected were confirmed of their binding by a novel mode of gel shift assay (fluorescence enhancement caused by the binding). Thus, novel Aβ42-binding peptides with high affinity were provided for the future Alzheimer's disease study. The demonstration of the effectiveness of the systemic in vitro evolution of PLM is very encouraging for the study of identifying novel functional Peptides
机译:最近的研究支持Aβ42寡聚体的产生是阿尔茨海默氏病的原因。因此,与Aβ42结合的那些肽在科学上是令人感兴趣的,并且可以是诊断和治疗阿尔茨海默氏病的候选者。最近开发的全身体外进化方法和指定的渐进文库方法(PLM)用于获得与Aβ42结合的适体肽。结果,通过这种方法可以鉴定出由8个或9个氨基酸组成的高亲和力的肽适体,方法论的有效性。即,证实了基于从初级文库选择获得的信息构建的来自多样化肽的二级文库的选择产物,如先前所报道的,其优于从初级文库中选择的那些。通过SPR(表面等离子体激元共振)测量的那些肽的亲和力与迄今为止报道的那些肽的亲和力相当或更高(Kd为10-7)。通过一种新型的凝胶位移测定法(结合引起的荧光增强),确认了所选择的其他肽的结合。因此,为今后的阿尔茨海默氏病研究提供了具有高亲和力的新型Aβ42结合肽。 PLM的体外系统进化的有效性的证明对于鉴定新型功能肽的研究非常令人鼓舞

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