利用病毒样颗粒进行诺如病毒无标记快速检测的生物层干涉生物传感器的评价

Xiuli Dong, Jessica Jenkins Broglie, Yongan Tang, Liju Yang
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引用次数: 1

摘要

本研究利用两种病毒样颗粒(VLPs)检测诺如病毒(NoV) GI.1和gi .4,评价了无标记生物层干涉(BLI)生物传感器检测诺如病毒(NoV)的效果。为了构建用于检测NoV GI.1和gi .4的生物传感器,预先固定了抗小鼠fc特异性抗体的商用AMC传感器,通过Blitz系统分别与捕获的抗体mAb3901和mAb NS14结合。捕获抗体在AMC传感器上的固定动力学表明,mAb3901和mAb NS14几乎同时达到饱和结合期(~415 s), mAb3901和mAb NS14的最佳固定捕获抗体浓度均为15 μg/mL。在相同的结合条件下,AMC传感器比mAb3901装载更多的单抗NS14。以最佳浓度固定捕获抗体构建的生物传感器与GI.1 VLPs和gi .4 VLPs具有紧密的结合作用,亲和常数分别为6.01 × 10-7 M和2.01 × 10-7 M。两种生物传感器的VLP结合率均随VLP浓度的增加而线性增加。这些生物传感器能够检测到PBS中浓度为5 μg/mL的GI.1或gi .4 VLPs,并且在VLP浓度为10 μg/mL及以上时表现出强烈而稳定的结合相互作用。mAb ns14固定化生物传感器检测gi .4 VLP的灵敏度高于mab3901固定化生物传感器检测GI.1 VLP的灵敏度。该检测技术无标记、简便、快速(2 min)、准确,样品体积极小(4 μL)。
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Evaluation of Bio-Layer Interferometric Biosensors for Label-Free Rapid Detection of Norovirus Using Virus Like Particles
This study evaluated the label-free bio-layer interferometric (BLI) biosensor for the detection of norovirus (NoV) using two types of virus like particles (VLPs) that represent human NoV GI.1 and GII.4. To construct biosensors for NoV GI.1 and GII.4 detection, the commercial AMC sensors, on which anti-mouse Fc-specific antibodies were preimmobilized on the surfaces, were further bound with the capture antibodies mAb3901 and mAb NS14, respectively, by using the Blitz system. The kinetics of immobilization of capture antibodies on the AMC sensors demonstrated that mAb3901 and mAb NS14 reached saturated binding phase almost at the same time (~415 s). The optimal concentration of capture antibodies for immobilization was 15 μg/mL for both mAb3901 and mAb NS14. The AMC sensors loaded more mAb NS14 than mAb3901 at the same binding condition. The biosensors constructed by immobilization of the capture antibodies at their optimal concentration showed tight binding interactions with their respective GI.1 VLPs and GII.4 VLPs, with the affinity constant of 6.01 × 10-7 M and 2.01 × 10-7 M, respectively. For both biosensors, the VLPs binding rates were linearly increased with the increase of VLP concentrations. These biosensors were able to detect GI.1 or GII.4 VLPs at the concentration of 5 μg/mL in PBS, and showed intense and stable binding interactions at VLP concentration of 10 μg/mL and above. The mAb NS14-immoblized biosensors for GII.4 VLP detection were more sensitive than the mAb3901-immoblized biosensors for GI.1 VLP detection. This detection technique was label-free, easy, rapid (2 min), and accurate, requiring a very small sample volume (4 μL).
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