获取途径

作者

Gang Wang Wen Liang Noshin Afshan Yuxin Lei Haoyu Li Yang Xiang Jin Jiao

作者单位

¹State Key Laboratory of Pharmaceutical Biotechnology, School of Life Sciences, Nanjing University, Nanjing, 210023, China ³Shandong Cancer Hospital and Institute, Shandong First Medical University & Shandong Academy of Medical Sciences, Jinan, 250117, China ²G.W. and W.L. contributed equally to this work.

刊名

Chemical Engineering Journal

年份

2025

卷号

Vol.524

页码

169463

ISSN

1385-8947

摘要

The integration of in vivo detection and liquid biopsy through engineered artificial biomarkers has garnered significant attention. These biomarkers overcome limitations of traditional liquid biopsy, such as low abundance and rapid clearance of endogenous biomarkers, by enabling quantifiable detection of disease-specific targets in body fluids. Herein, we report a spherical peptide nucleic acid -based artificial biomarker system for ultrasensitive analysis of tumor-associated Cathepsin B . The ...更多

The integration of in vivo detection and liquid biopsy through engineered artificial biomarkers has garnered significant attention. These biomarkers overcome limitations of traditional liquid biopsy, such as low abundance and rapid clearance of endogenous biomarkers, by enabling quantifiable detection of disease-specific targets in body fluids. Herein, we report a spherical peptide nucleic acid -based artificial biomarker system for ultrasensitive analysis of tumor-associated Cathepsin B . The GPP system comprises AuNP-loaded tandem peptide-PNA probes, where the peptide serves as a CB-responsive substrate and linker, while the enzymatically stable PNA acts as a shielded reporter. Upon CB-mediated cleavage in tumor tissues, PNA probes are released into circulation, excreted via urine, and detected using an Nb.BbvCI-assisted DNA walker based electrochemical sensor. The sensor leverages competitive binding between PNA and a locked DNA walker to trigger methylene blue signal amplification. In vitro and in vivo studies demonstrated that GPP achieves a detection limit of 17.5 pg/ mL for CB, exhibits robust stability under enzymatic and physiological challenges, and enables tumor-specific fluorescence/electrochemical signal readouts within 2–3 h of post-injection. This work pioneers a multi-functional, enzyme-responsive nanoplatform for non-invasive tumor diagnosis, combining the programmability of PNA with the sensitivity of electrochemical sensing.收起

文献类型

期刊

浏览量

8