Functionalized Terpolymer-Brush-Based Biointerface with Improved Antifouling Properties for Ultra-Sensitive Direct Detection of Virus in Crude Clinical Samples

生物界面 检出限 材料科学 生物传感器 纳米技术 生物污染 色谱法 病毒学 化学 生物 生物化学
作者
Michala Forinová,Alina Pilipenco,Ivana Víšová,N. Scott Lynn,Jakub Dostálek,Hana Mašková,Václav Hönig,Martin Palus,Martin Selinger,Pavlína Kočová,Filip Dyčka,Ján Štěrba,Milan Houška,Markéta Vrabcová,Petr Horák,Judita Anthi,Chao-Ping Tung,Chung-Ming Yu,Chi-Yung Chen,Yu-Chuan Huang,Pei-Hsun Tsai,Szu‐Yu Lin,Hung-Ju Hsu,An‐Suei Yang,A. Dejneka,Hana Vaisocherová‐Lísalová
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:13 (50): 60612-60624 被引量:33
标识
DOI:10.1021/acsami.1c16930
摘要

New analytical techniques that overcome major drawbacks of current routinely used viral infection diagnosis methods, i.e., the long analysis time and laboriousness of real-time reverse-transcription polymerase chain reaction (qRT-PCR) and the insufficient sensitivity of "antigen tests", are urgently needed in the context of SARS-CoV-2 and other highly contagious viruses. Here, we report on an antifouling terpolymer-brush biointerface that enables the rapid and sensitive detection of SARS-CoV-2 in untreated clinical samples. The developed biointerface carries a tailored composition of zwitterionic and non-ionic moieties and allows for the significant improvement of antifouling capabilities when postmodified with biorecognition elements and exposed to complex media. When deployed on a surface of piezoelectric sensor and postmodified with human-cell-expressed antibodies specific to the nucleocapsid (N) protein of SARS-CoV-2, it made possible the quantitative analysis of untreated samples by a direct detection assay format without the need of additional amplification steps. Natively occurring N-protein-vRNA complexes, usually disrupted during the sample pre-treatment steps, were detected in the untreated clinical samples. This biosensor design improved the bioassay sensitivity to a clinically relevant limit of detection of 1.3 × 104 PFU/mL within a detection time of only 20 min. The high specificity toward N-protein-vRNA complexes was validated both by mass spectrometry and qRT-PCR. The performance characteristics were confirmed by qRT-PCR through a comparative study using a set of clinical nasopharyngeal swab samples. We further demonstrate the extraordinary fouling resistance of this biointerface through exposure to other commonly used crude biological samples (including blood plasma, oropharyngeal, stool, and nasopharyngeal swabs), measured via both the surface plasmon resonance and piezoelectric measurements, which highlights the potential to serve as a generic platform for a wide range of biosensing applications.

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