Zhang Zhengyao, Li Zhi, Jin Yuhang, Gao Xu, Zhu Zekai, Zhang Hangyu, Wu Bin, Liu Bo
Department of Clinical Laboratory, Central Hospital of Dalian University of Technology, Dalian 116033, China.
School of Chemical Engineering, Ocean and Life Sciences, Dalian University of Technology, Panjin 124221, China.
ACS Omega. 2025 Jun 24;10(26):28083-28091. doi: 10.1021/acsomega.5c02356. eCollection 2025 Jul 8.
Colloidal gold immunochromatography has emerged as a pivotal platform for point-of-care diagnostics, yet challenges persist in stabilizing nanoparticle-antibody interactions and ensuring batch-to-batch reproducibility. To address these limitations, we engineered a nanogold-affinity peptide probe for the rapid detection of the lung cancer biomarker carcinoembryonic antigen (CEA), leveraging phage-display-derived peptides as biorecognition elements. The probe was synthesized by conjugating CEA-specific affinity peptides to polyethylene glycol (PEG)-functionalized gold nanoparticles (AuNPs) via covalent amide bonding, ensuring precise orientation and enhanced colloidal stability. Systematic optimization of reaction parameters, including the PEGylation time, peptide-to-nanoparticle ratios, and centrifugation conditions, yielded a robust preparation protocol. The resulting immunochromatographic test strip demonstrated a detection limit of 2.5 ng/mL for CEA, surpassing the clinical threshold of 5 ng/mL, and exhibited 91.7% accuracy in clinical serum samples. Notably, the substitution of antibodies with synthetic affinity peptides reduced costs by approximately 8-fold while maintaining high specificity and resistance to nonspecific binding. This work not only advances the integration of biomolecular engineering and nanotechnology for diagnostic applications but also establishes a scalable framework for developing stable, low-cost biosensors targeting macromolecular biomarkers.
胶体金免疫层析已成为即时诊断的关键平台,但在稳定纳米颗粒与抗体的相互作用以及确保批次间的可重复性方面仍存在挑战。为解决这些局限性,我们设计了一种纳米金亲和肽探针,用于快速检测肺癌生物标志物癌胚抗原(CEA),利用噬菌体展示衍生的肽作为生物识别元件。该探针通过将CEA特异性亲和肽通过共价酰胺键与聚乙二醇(PEG)功能化的金纳米颗粒(AuNPs)偶联合成,确保了精确的取向并增强了胶体稳定性。对反应参数进行系统优化,包括聚乙二醇化时间、肽与纳米颗粒的比例以及离心条件,得到了一个稳健的制备方案。所得的免疫层析试纸条对CEA的检测限为2.5 ng/mL,超过了5 ng/mL的临床阈值,并且在临床血清样本中表现出91.7%的准确率。值得注意的是,用合成亲和肽替代抗体可将成本降低约8倍,同时保持高特异性和抗非特异性结合能力。这项工作不仅推动了生物分子工程和纳米技术在诊断应用中的整合,还建立了一个可扩展的框架,用于开发针对大分子生物标志物的稳定、低成本生物传感器。