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基于抗体的生物微系统中结核分枝杆菌 ESAT-6 的生物电化学检测。

Bioelectrochemical Detection of Mycobacterium tuberculosis ESAT-6 in an Antibody-Based Biomicrosystem.

机构信息

CMUA, Department of Electrical and Electronics Engineering, Universidad de los Andes, 111711 Bogota, Colombia.

CorpoGen, Carrera 5 No. 66A-34, 110231 Bogota, Colombia.

出版信息

Sensors (Basel). 2017 Sep 22;17(10):2178. doi: 10.3390/s17102178.

Abstract

Bioelectrochemical sensing of through electro-immunosensors is a promising technique to detect relevant analytes. In general, immunosensors require the formation of organic assemblies by the adsorption of molecular constituents. Moreover, they depend on the correct immobilization of the bio-recognition element in the biosensor. These procedures cannot be easily monitored without the use of invasive methods. In this work, an impedance analysis technique was used, as a non-invasive method, to measure and differentiate the manufacturing stages of the sensors. Biomicrosystems were fabricated through physical vapor deposition (PVD) of 80 nm Au nanolayers on 35 µm copper surfaces. Later, the surface was modified through thiolation methods generating a self-assembled-monolayer (SAM) with 20 mM 4-aminothiophenol (4-ATP) on which a polyclonal antibody (pAb) was covalently attached. Using impedance analysis, every step of the electro-immunosensor fabrication protocol was characterized using 40 independent replicas. Results showed that, compared to the negative controls, distilled water, and 0.5 µg/mL HSA, a maximum variation of 171% between each replica was achieved when compared to samples containing 0.5 µg/mL of ESAT-6 immunodominant protein. Therefore, this development validates a non-invasive method to electrically monitor the assembly process of electro-immunosensors and a tool for its further measure for detection of relevant antigens.

摘要

通过电免疫传感器对 ESAT-6 进行生物电化学传感是一种很有前途的检测相关分析物的技术。一般来说,免疫传感器需要通过分子成分的吸附形成有机组装体。此外,它们依赖于生物识别元件在生物传感器中的正确固定化。如果不使用侵入性方法,这些过程就无法轻易监测。在这项工作中,我们使用阻抗分析技术作为一种非侵入性方法来测量和区分传感器的制造阶段。生物微系统是通过在 35 µm 铜表面上物理气相沉积(PVD)80nm 的 Au 纳米层来制造的。随后,通过巯基化方法对表面进行修饰,生成具有 20mM 4-氨基硫代苯酚(4-ATP)的自组装单层(SAM),在其上共价连接多克隆抗体(pAb)。使用阻抗分析,通过 40 个独立复制品对电免疫传感器制造协议的每一步进行了表征。结果表明,与阴性对照、蒸馏水和 0.5 µg/mL HSA 相比,当比较含有 0.5 µg/mL ESAT-6 免疫显性蛋白的样品时,每个复制品之间的最大差异达到 171%。因此,该研究验证了一种非侵入性方法,可用于电监测电免疫传感器的组装过程,并且是对其进一步检测相关抗原的工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6bf/5676732/68681a24257b/sensors-17-02178-g001a.jpg

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