A COVID19-selective pH-paper test: Ultrafast and highly accurate antibody-free viral detection in native saliva

唾液 病毒学 蛋白酵素 注意事项 严重急性呼吸综合征冠状病毒2型(SARS-CoV-2) 抗体 生物素化 2019年冠状病毒病(COVID-19) 生物 化学 免疫学 医学 分子生物学 生物化学 传染病(医学专业) 疾病 护理部 病理
作者
Ella Borberg,Sofiya Pashko,Fernando Patolsky
出处
期刊:Chemical Engineering Journal [Elsevier BV]
卷期号:475: 146304-146304
标识
DOI:10.1016/j.cej.2023.146304
摘要

COVID-19 is caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). SARS-CoV-2 has led to high mortality worldwide, with social and financial effects expected to persist for years to come. Since asymptomatic individuals cause a large portion of transmission, actions taken to curb the COVID-19 pandemic mostly rely on procedures aimed at detecting viral-related molecules in infected carriers. Currently, leading available detection methods fall short in reliability or point-of-care mass screening applicability. Here, we present an unprecedented antibody-free smart pH paper-based seconds-long detection platform against the virus-related enzyme 3CLpro as a saliva biomarker of SARS-CoV-2 infection. The selective proteolytic activity of 3CLpro is directly detected from native saliva using a peptide substrate-embedded pH-paper platform. 3CLpro presence in infected individuals leads to an ultrafast pH-drop in the paper matrix, thus leading to a sharp color change as direct means of detection. Ultrafast detection, simplicity, no requirement of surface chemistry by sensitive biomolecules, long-term stability, and point-of-care compatibility for COVID-19 mass screening were demonstrated. Forty-two subjects were tested, exhibiting highly sensitive and specific detection of SARS-CoV-2 infection. Finally, we foresee that this universal approach could be implemented for the multiplexed detection of other viral infections by detecting specific viral proteases. Importantly, since our approach does not require immune-specific antibodies for specific detection, the overall platform is extremely cost-efficient, less than 2 USD cents per assay, and suitable for the worldwide mass screening of viral infections, particularly in remote and developing world locations. Moreover, we propose an extremely easy-to-use and produce practical test strip design.

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