<p>Carcinoembryonic antigen (CEA) is a clinically significant biomarker for early-stage cancer diagnosis and therapeutic monitoring. Conventional immunoassays, while effective, suffer from limitations in stability, sensitivity, and procedural complexity. In this work, we report a label-free nanozyme electrochemical biosensor (nanoE-EB) integrating self-assembled peptide-templated Au/Cu bimetallic nanozymes for selective and sensitive CEA detection, eliminating labeling steps. The amphiphilic peptide i<sub>3</sub>k self-assembles into nanofibers that serve as biocompatible scaffolds for the uniform anchoring of Au/Cu nanoparticles with an optimized 4:1 molar ratio. This architecture enhances peroxidase-like catalytic activity through synergistic redox interactions between Cu<sup>2+</sup>/Cu<sup>+</sup> and Au0 sites. A ferrocene-functionalized chitosan matrix facilitates rapid electron transfer, augmenting signal transduction. The resulting biosensor displays a wide dynamic range (1.25–200&#xa0;ng/mL), a low detection limit (0.15&#xa0;ng/mL), and excellent specificity and reproducibility in protein-rich matrices, achieving recoveries&#xa0;of 87.05–115.85% in spiked serum samples. This integrated platform demonstrates catalytic amplification, structural precision, and electrochemical reliability, offering a sustainable and scalable strategy for point-of-care cancer diagnostics.&#xa0;</p> Graphical Abstract <p></p>

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Development of a label-free electrochemical immunosensor based on self-assembled peptide-templated Au/Cu bimetallic nanozymes for sensitive detection of carcinoembryonic antigen (CEA)

  • Linyou Mao,
  • Mengfei Li,
  • Zihao Li,
  • Yonghai Feng,
  • Lei Liu,
  • Rong Qin,
  • Liang Yuan

摘要

Carcinoembryonic antigen (CEA) is a clinically significant biomarker for early-stage cancer diagnosis and therapeutic monitoring. Conventional immunoassays, while effective, suffer from limitations in stability, sensitivity, and procedural complexity. In this work, we report a label-free nanozyme electrochemical biosensor (nanoE-EB) integrating self-assembled peptide-templated Au/Cu bimetallic nanozymes for selective and sensitive CEA detection, eliminating labeling steps. The amphiphilic peptide i3k self-assembles into nanofibers that serve as biocompatible scaffolds for the uniform anchoring of Au/Cu nanoparticles with an optimized 4:1 molar ratio. This architecture enhances peroxidase-like catalytic activity through synergistic redox interactions between Cu2+/Cu+ and Au0 sites. A ferrocene-functionalized chitosan matrix facilitates rapid electron transfer, augmenting signal transduction. The resulting biosensor displays a wide dynamic range (1.25–200 ng/mL), a low detection limit (0.15 ng/mL), and excellent specificity and reproducibility in protein-rich matrices, achieving recoveries of 87.05–115.85% in spiked serum samples. This integrated platform demonstrates catalytic amplification, structural precision, and electrochemical reliability, offering a sustainable and scalable strategy for point-of-care cancer diagnostics. 

Graphical Abstract