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Antimicrobial Peptides for Detection of Bacteria in Biosensor Assays

机译:在生物传感器分析中用于检测细菌的抗菌肽

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Bacteria, plants, and higher and lower animals have evolved an innate immune system as a first line of defense against microbial invasion. Some of these organisms produce antimicrobial peptides (AMPs) as a part of this chemical immune system. AMPs exert their antimicrobial activity by binding to components of the microbe's surface and disrupting the membrane. The overall goal of this study was to apply the AMP magainin I as a recognition element for Escherichia coli O157:H7 and Salmonella typhimurium detection on an array-based biosensor. We immobilized magainin I on silanized glass slides using biotin-avidin chemistry, as well as through direct covalent attachment. Cy5-labeled, heat-killed cells were used to demonstrate that the immobilized magainin I can bind Salmonella with detection limits similar to analogous antibody-based assays. Detection limits for E. coli were higher than in analogous antibody-based assays, but it is expected that other AMPs may possess higher affinities for this target. The results showed that both specific and nonspecific binding strongly depend on the method used for peptide immobilization. Direct attachment of magainin to the substrate surface not only decreased nonspecific cell binding but also resulted in improved detection limits for both Salmonella and E. coli.
机译:细菌,植物以及高等和低等动物已经进化出先天免疫系统,作为抵抗微生物入侵的第一道防线。这些生物中的一些会产生抗微生物肽(AMP),作为这种化学免疫系统的一部分。 AMP通过结合微生物表面的成分并破坏膜而发挥其抗菌活性。这项研究的总体目标是将AMP magainin I用作基于阵列生物传感器的大肠杆菌O157:H7和鼠伤寒沙门氏菌检测的识别元件。我们使用生物素-亲和素化学方法以及通过直接共价连接将magainin I固定在硅烷化的载玻片上。 Cy5标记的热灭活细胞用于证明固定化的magainin I可以结合类似于基于抗体的检测方法的检测限结合沙门氏菌。大肠杆菌的检出限高于类似的基于抗体的测定法,但预计其他AMP对该靶标可能具有更高的亲和力。结果表明特异性和非特异性结合都强烈依赖于用于肽固定的方法。麦角菌素直接附着于底物表面不仅降低了非特异性细胞结合,而且还提高了沙门氏菌和大肠杆菌的检测限。

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