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基于适体-抗体夹心结构形成的磁助力电化学传感器检测凝血酶。

Magnetic force assisted electrochemical sensor for the detection of thrombin with aptamer-antibody sandwich formation.

机构信息

Department of Chemistry, Pusan National University, 2 Busandaehak-ro 63beon-gil, Geumjeong-gu, Busan 46241, Republic of Korea.

BBB Inc., 26 Samseong-ro 85-gil, Gangnam-gu, Seoul 06194, Republic of Korea.

出版信息

Biosens Bioelectron. 2018 Oct 15;117:480-486. doi: 10.1016/j.bios.2018.06.068. Epub 2018 Jul 5.

Abstract

A magnetic force assisted electrochemical aptamer-antibody sandwich assay (MESA) was developed for the detection of thrombin as a model protein in serum samples. The MESA using the formation of sandwich complexes on the electrochemical sensor probe for reaction and the removal of unbound bioconjugates from the sensor surface without washing are controlled by a magnetic field. Thrombin was determined by the cathodic currents of a toluidine blue O (TBO) attached with thrombin antibody modified magnetic nanoparticle (MNP) at the sensor surface. To detect thrombin in a serum sample, we applied a thrombin-specific aptamer as the capture molecule bound to the functionalized conducting polymer layer (poly-(2,2´:5´,5″-terthiophene-3´-p-benzoic acid) (pTBA)), and streptavidin and starch coated-MNP was conjugated with biotinylated thrombin antibodies (Ab) and TBO as the bioconjugate (MNP@Ab-TBO). The characterization of MNP@Ab-TBO and sensor probe was performed using voltammetry, impedance spectroscopy, XPS, and UV-VIS spectroscopy. The experimental conditions were optimized in terms of pH, binding time, removal time of unbound bioconjugates, and applied potential. The dynamic ranges of thrombin were from 1.0 to 500 nM with detection limit of 0.49 ( ± 0.06) nM. The recovery test demonstrates the reliability of the proposed sensing system for a handheld device.

摘要

一种基于磁助力电化学适体-抗体三明治法(MESA)的凝血酶检测方法被开发出来,用于检测血清样品中的凝血酶。该方法利用三明治复合物在电化学传感器探针上的形成,以及在无需洗涤的情况下通过磁场控制从传感器表面去除未结合的生物缀合物。凝血酶通过修饰在传感器表面上的凝血酶抗体的甲苯胺蓝 O(TBO)的阴极电流来测定。为了检测血清中的凝血酶,我们应用了一种凝血酶特异性适体作为与功能化导电聚合物层(聚(2,2':5',5''-三联噻吩-3'-对苯甲酸)(pTBA))结合的捕获分子,并将链霉亲和素和淀粉包被的磁纳米粒子(MNP)与生物素化的凝血酶抗体(Ab)和 TBO 缀合作为生物缀合物(MNP@Ab-TBO)。通过伏安法、阻抗谱、XPS 和紫外可见光谱对 MNP@Ab-TBO 和传感器探针进行了表征。优化了 pH 值、结合时间、未结合生物缀合物的去除时间和施加电位等实验条件。凝血酶的动态范围为 1.0 至 500 nM,检测限为 0.49(±0.06)nM。回收测试证明了该传感系统对于手持式设备的可靠性。

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