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钒单原子配位人工过氧化物酶用于生物催化剂联免疫吸附测定法检测高灵敏度癌胚抗原

Vanadium single-atoms coordinated artificial peroxidases as biocatalyst-linked immunosorbent assay for highly-sensitive carcinoembryonic antigen immunoassay.

作者信息

Yuan Minjia, Yan Rui, Zhao Zhenyang, Wen Qinlong, Xie Xiaodong, Adeli Mohsen, Li Shuang, Cheng Chong

机构信息

College of Polymer Science and Engineering, State Key Laboratory of Polymer Materials Engineering, Sichuan University, Chengdu, 610065, China.

Department of Biotherapy, Cancer Center, West China Hospital, Sichuan University, Chengdu, 610041, China.

出版信息

Biomaterials. 2025 May;316:123008. doi: 10.1016/j.biomaterials.2024.123008. Epub 2024 Dec 14.

Abstract

In medical and biomedical fields, enzyme-mimetic nanomaterials have garnered significant interest as efficacious signal enhancers for biocatalyst-linked immunosorbent assays (BLISA). Despite the burgeoning enthusiasm, engineering artificial biocatalysts that exhibit both exceptional catalytic proficiency and pronounced colorimetric signal output remains a formidable challenge. Inspired by the heme structures and biocatalytic activities of horseradish peroxidase, we introduce the synthesis of vanadium single-atoms (SAV) coordinated artificial peroxidases as BLISA for highly sensitive and selective carcinoembryonic antigen (CEA) immunoassay. Our synthesized SAV exhibits peroxidase (POD)-like activity that is both efficacious and highly specific, surpassing the performance of many other single-atom-structured materials. The SAV-linked immunoassay demonstrates an ultrasensitive response to the target antigen (CEA), with a linear detection range spanning 0.03-10 ng/mL and an impressively low detection limit of 0.335 ng/mL. This straightforward and robust immunoassay technique not only achieves superior signal amplification compared to traditional natural enzymes but also boasts high precision, commendable reproducibility, and remarkable specificity, aligning closely with conventional enzyme-linked immunosorbent assay for CEA detection in serum samples. This study offers a blueprint for designing artificial peroxidase-based colorimetric nanosystems, promoting the evolution of ultrasensitive BLISA applications for the early diagnosis and intervention of cancer.

摘要

在医学和生物医学领域,模拟酶纳米材料作为生物催化剂联免疫吸附测定法(BLISA)的有效信号增强剂已引起广泛关注。尽管热情高涨,但设计出兼具卓越催化能力和显著比色信号输出的人工生物催化剂仍然是一项艰巨的挑战。受辣根过氧化物酶的血红素结构和生物催化活性的启发,我们介绍了钒单原子(SAV)配位人工过氧化物酶的合成,用于高灵敏度和选择性癌胚抗原(CEA)免疫测定的BLISA。我们合成的SAV表现出高效且高度特异性的过氧化物酶(POD)样活性,超过了许多其他单原子结构材料的性能。SAV联免疫测定对目标抗原(CEA)表现出超灵敏响应,线性检测范围为0.03 - 10 ng/mL,检测限低至0.335 ng/mL。这种简单而稳健的免疫测定技术不仅与传统天然酶相比实现了卓越的信号放大,还具有高精度、良好的重现性和显著的特异性,与血清样本中CEA检测的传统酶联免疫吸附测定法非常吻合。本研究为设计基于人工过氧化物酶的比色纳米系统提供了蓝图,推动了用于癌症早期诊断和干预的超灵敏BLISA应用的发展。

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