首页> 美国卫生研究院文献>Sensors (Basel Switzerland) >Versatile Protein-A Coated Photoelectric Immunosensors with a Purple-Membrane Monolayer Transducer Fabricated by Affinity-Immobilization on a Graphene-Oxide Complexed Linker and by Shear Flow
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Versatile Protein-A Coated Photoelectric Immunosensors with a Purple-Membrane Monolayer Transducer Fabricated by Affinity-Immobilization on a Graphene-Oxide Complexed Linker and by Shear Flow

机译:通过亲和固定在石墨烯-氧化物复合连接体上并通过剪切流制备的具有紫色膜单层传感器的多功能蛋白A涂层光电免疫传感器

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摘要

Bacteriorhodopsin-embedded purple membranes (PM) have been demonstrated to be a sensitive photoelectric transducer for microbial detection. To efficiently prepare versatile BR-based immunosensors with protein A as antibody captures, a large, high-coverage, and uniformly oriented PM monolayer was fabricated on an electrode as an effective foundation for protein A conjugation through bis-NHS esters, by first affinity-coating biotinylated PM on an aminated surface using a complex of oxidized avidin and graphene oxide as the planar linker and then washing the coating with a shear flow. Three different polyclonal antibodies, each against Escherichia coli, Lactobacillus acidophilus, and Streptococcus mutans, respectively, were individually, effectively and readily adsorbed on the protein A coated electrodes, leading to selective and sensitive quantitative detection of their respective target cells in a single step without any labeling. A single-cell detection limit was achieved for the former two cells. AFM, photocurrent, and Raman analyses all displayed each fabricated layer as well as the captured bacteria, with AFM particularly revealing the formation of a massive continuous PM monolayer on aminated mica. The facile cell-membrane monolayer fabrication and membrane surface conjugation techniques disclosed in this study may be widely applied to the preparation of different biomembrane-based biosensors.
机译:细菌视紫红质包埋的紫色膜(PM)已被证明是用于微生物检测的灵敏光电传感器。为了有效地制备具有蛋白A作为抗体捕获物的基于BR的多功能免疫传感器,在电极上制备了一个大的,高覆盖率且方向均匀的PM单层,作为通过双亲和力(NHS)酯通过第一亲和力进行蛋白A缀合的有效基础。使用氧化的亲和素和氧化石墨烯的复合物作为平面连接剂,在胺化的表面上涂覆生物素化的PM,然后用剪切流洗涤涂层。分别针对大肠杆菌,嗜酸乳杆菌和变形链球菌的三种不同的多克隆抗体分别,有效且容易地吸附在蛋白A包被的电极上,从而可在一个步骤中选择性,灵敏地定量检测各自的靶细胞而无需任何标签。前两个细胞达到了单细胞检测极限。 AFM,光电流和拉曼分析都显示了每个制造的层以及捕获的细菌,其中AFM特别显示了胺化云母上大量连续的PM单层的形成。这项研究中公开的简便的细胞膜单层制造和膜表面结合技术可能会广泛应用于不同的基于生物膜的生物传感器的制备。

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