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基于量子点纳米粒子的通用荧光免疫层析法快速检测 SARS-CoV-2 核衣壳蛋白特异性抗体。

A Universal Fluorescent Immunochromatography Assay Based on Quantum Dot Nanoparticles for the Rapid Detection of Specific Antibodies against SARS-CoV-2 Nucleocapsid Protein.

机构信息

School of Life Science, Zhengzhou University, Zhengzhou 450001, China.

School of Advanced Agriculture Sciences, Peking University, Beijing 100871, China.

出版信息

Int J Mol Sci. 2022 Jun 2;23(11):6225. doi: 10.3390/ijms23116225.

Abstract

Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) is the pathogenic agent leading to COVID-19. Due to high speed of transmission and mutation rates, universal diagnosis and appropriate prevention are still urgently needed. The nucleocapsid protein of SARS-CoV-2 is considered more conserved than spike proteins and is abundant during the virus' life cycle, making it suitable for diagnostic applications. Here, we designed and developed a fluorescent immunochromatography assay (FICA) for the rapid detection of SARS-CoV-2-specific antibodies using ZnCdSe/ZnS QDs-conjugated nucleocapsid (N) proteins as probes. The nucleocapsid protein was expressed in and purified via Ni-NTA affinity chromatography with considerable concentration (0.762 mg/mL) and a purity of more than 90%, which could bind to specific antibodies and the complex could be captured by protein A (SPA) with fluorescence displayed. After the optimization of coupling and detecting conditions, the limit of detection was determined to be 1:1.024 × 10 with an IgG concentration of 48.84 ng/mL with good specificity shown to antibodies against other zoonotic coronaviruses and respiratory infection-related viruses ( = 5). The universal fluorescent immunochromatography assay simplified operation processes in one step, which could be used for the point of care detection of SARS-CoV-2-specific antibodies. Moreover, it was also considered as an efficient tool for the serological screening of potential susceptible animals and for monitoring the expansion of virus host ranges.

摘要

严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)是导致 COVID-19 的病原体。由于其传播速度快、突变率高,因此仍然迫切需要进行通用诊断和适当的预防。SARS-CoV-2 的核衣壳蛋白被认为比刺突蛋白更保守,并且在病毒生命周期中大量存在,使其成为适合诊断应用的选择。在这里,我们设计并开发了一种荧光免疫层析测定法(FICA),用于快速检测 SARS-CoV-2 特异性抗体,使用 ZnCdSe/ZnS QD 偶联的核衣壳(N)蛋白作为探针。核衣壳蛋白在 中表达,并通过 Ni-NTA 亲和层析进行纯化,具有相当高的浓度(0.762 mg/mL)和超过 90%的纯度,可与特异性抗体结合,并且复合物可被 SPA 捕获,显示出荧光。在优化偶联和检测条件后,确定检测限为 1:1.024×10,IgG 浓度为 48.84 ng/mL,对其他人畜共患冠状病毒和呼吸道感染相关病毒的抗体具有良好的特异性( = 5)。通用荧光免疫层析测定法简化了一步操作流程,可用于即时检测 SARS-CoV-2 特异性抗体。此外,它还被认为是一种用于监测病毒宿主范围扩大的潜在易感动物的血清学筛选的有效工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc83/9180975/ea1b456266c1/ijms-23-06225-g001.jpg

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