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MRPAND: A one-tube multiplex ago-mediated nucleic acid detection platform for visualized EGFR genotyping in point-of-care settings.

Talanta 2026 Vol.306() p. 129696 Biosensors and Analytical Detection
OpenAlex 토픽 · Biosensors and Analytical Detection Gene expression and cancer classification Advanced Biosensing Techniques and Applications

Fu J, Yang J, Shang Q, Si W, Shi S

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Current nucleic detection techniques suffer from prolonged timelines, high false-positive amplification, and poor point-of-care testing (POCT) compatibility, especially for multiplex assays.

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APA Jinyu Fu, Jiaming Yang, et al. (2026). MRPAND: A one-tube multiplex ago-mediated nucleic acid detection platform for visualized EGFR genotyping in point-of-care settings.. Talanta, 306, 129696. https://doi.org/10.1016/j.talanta.2026.129696
MLA Jinyu Fu, et al.. "MRPAND: A one-tube multiplex ago-mediated nucleic acid detection platform for visualized EGFR genotyping in point-of-care settings.." Talanta, vol. 306, 2026, pp. 129696.
PMID 41903381

Abstract

Current nucleic detection techniques suffer from prolonged timelines, high false-positive amplification, and poor point-of-care testing (POCT) compatibility, especially for multiplex assays. This highlights an urgent need for efficient diagnostics, particularly for the Epidermal Growth Factor Receptor (EGFR), a critical biomarker for non-small cell lung cancer (NSCLC) assessment, therapy, and postoperative monitoring. In this study, we established a one-tube detection platform, termed MRPAND, that integrates Multiplex Recombinant Polymerase Amplification (RPA) with Pyrococcus furiosus Argonaute-mediated Nucleic Acid Detection (PAND) for the identification of EGFR mutations. Capitalizing on the cleavage principle of PfAgo, the system enables simultaneous discrimination of two distinct mutations with high specificity. By integrating RPA with a lateral flow strip (LFS), the system achieves a sensitivity of 1 copy/μL with naked-eye visual readout, requires no sophisticated instrumentation, and is therefore well-suited for POCT applications. We further validated the clinical applicability of MRPAND using clinical samples, demonstrating its capability to identify EGFR mutations. These results underscore the potential of MRPAND as a promising diagnostic tool in lung cancer care.

MeSH Terms

ErbB Receptors; Humans; Lung Neoplasms; Pyrococcus furiosus; Point-of-Care Systems; Point-of-Care Testing; Carcinoma, Non-Small-Cell Lung; Argonaute Proteins; Mutation; Nucleic Acid Amplification Techniques; Nucleic Acids; Genotyping Techniques; Genotype

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