4.8 Article

Ultrasensitive Electrochemical Detection of Mutated Viral RNAs with Single-Nucleotide Resolution Using a Nanoporous Electrode Array (NPEA)

Journal

ACS NANO
Volume 16, Issue 4, Pages 5764-5777

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsnano.1c10824

Keywords

electrochemical nanobiosensors; detection of nucleic acids; detection of single point mutation; mismatched nucleic acid-metal ion (MNM) nanocomplex; nanoporous electrode array (NPEA); multiplexed detection; SARS-CoV-2

Funding

  1. NSF [CHE-1429062]
  2. NJHF [PC16-21CV]
  3. Rutgers Global Health Grant
  4. National Research Foundation of Korea (NRF) - Korean government (MSIT) [2019R1A2C3002300]
  5. National R&D Program through the National Research Foundation of Korea (NRF) - Ministry of Science and ICT [NRF-2022M3H4A1A01005271]
  6. New Jersey Commission on Cancer Research [SNJ-CCR-DCHS20PPC043]
  7. National Research Foundation of Korea [2022M3H4A1A01005271] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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The detection of nucleic acids and their mutation derivatives is crucial in biomedical science and applications. Current nucleic acid biosensors often require pretreatment processes and cannot detect specific sequence mutations. To overcome these limitations, a novel electrochemical nano-biosensing system was developed using metal ion intercalation and a gold nanoporous electrode array. This system enables sensitive detection of viral RNA, determination of viral mutation occurrence, and multiplexed detection of multiple RNA targets simultaneously.
The detection of nucleic acids and their mutation derivatives is vital for biomedical science and applications. Although many nucleic acid biosensors have been developed, they often require pretreatment processes, such as target amplification and tagging probes to nucleic acids. Moreover, current biosensors typically cannot detect sequence-specific mutations in the targeted nucleic acids. To address the above problems, herein, we developed an electrochemical nano-biosensing system using a phenomenon comprising metal ion intercalation into the targeted mismatched double-stranded nucleic acids and a homogeneous Au nanoporous electrode array (Au NPEA) to obtain (i) sensitive detection of viral RNA without conventional tagging and amplifying processes, (ii) determination of viral mutation occurrence in a simple detection manner, and (iii) multiplexed detection of several RNA targets simultaneously. As a proof-of-concept demonstration, a SARS-CoV-2 viral RNA and its mutation derivative were used in this study. Our developed nanobiosensor exhibited highly sensitive detection of SARS-CoV-2 RNA (similar to 1 fM detection limit) without tagging and amplifying steps. In addition, a single point mutation of SARS-CoV-2 RNA was detected in a one-step analysis. Furthermore, multiplexed detection of several SARS-CoV-2 RNAs was successfully demonstrated using a single chip with four combinatorial NPEAs generated by a 3D printing technique. Collectively, our developed nanobiosensor provides a promising platform technology capable of detecting various nucleic acids and their mutation derivatives in highly sensitive, simple, and time-effective manners for point-of-care biosensing.

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