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基于金钯纳米粒子过氧化物酶样活性的空肠弯曲菌细胞比色适体传感器。

Colorimetric aptasensor for Campylobacter jejuni cells by exploiting the peroxidase like activity of Au@Pd nanoparticles.

机构信息

Department of Life Science Engineering, Faculty of New Sciences & Technologies, University of Tehran, Tehran, 1417466191, Iran.

Department of Pharmaceutical Biomaterials and Medical Biomaterials Research Center, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran.

出版信息

Mikrochim Acta. 2018 Sep 5;185(10):448. doi: 10.1007/s00604-018-2976-2.

Abstract

The authors describe a method for colorimetric determination of Campylobacter jejuni (C. jejuni) in milk samples. It is based on the interaction of a specific DNA aptamer with surface protein in the cell membranes of C. jejuni. Specific binding of the aptamer with the cell membrane leads to an uptake of aptamer from solution. As a result, the concentration of aptamer floating in the solution is reduced. In the presence of large quantities of aptamer, the surface of added Au@Pd nanoparticles (NPs) is covered with aptamer via electrostatic interactions. Hence, they cannot act as a peroxidase mimic and oxidize the substrate 3,3,5,5-tetramethylbenzidine (TMB) to give a blue product. However, when the aptamer is bound by the target cells, the surface of the NPs is not blocked by aptamer and the NPs exert a strong peroxidase -like activity. Under defined experimental conditions, the intensity of the blue color increases with the concentration of C. jejuni, and as little as 100 CFU·mL can bedetected in milk. Graphical abstract A colorimetric aptasensor for assay Campylobacter jejuni whole cell in food samples was investigated. This assay was designed based on interaction of specific DNA aptamer with surface protein in c. jejuni cell membrane without any modification of aptamer.

摘要

作者描述了一种用于检测牛奶样品中弯曲杆菌(C. jejuni)的比色法。它基于特定 DNA 适体与 C. jejuni 细胞膜表面蛋白的相互作用。适体与细胞膜的特异性结合导致适体从溶液中被吸收。结果,溶液中漂浮的适体浓度降低。在大量适体存在的情况下,添加的 Au@Pd 纳米颗粒(NPs)的表面通过静电相互作用被适体覆盖。因此,它们不能充当过氧化物酶模拟物,并氧化底物 3,3,5,5-四甲基联苯胺(TMB)以产生蓝色产物。然而,当适体与靶细胞结合时,NPs 的表面不会被适体阻断,并且 NPs 发挥出强烈的过氧化物酶样活性。在规定的实验条件下,蓝色强度随 C. jejuni 浓度的增加而增加,在牛奶中可检测到低至 100 CFU·mL。

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