AI-Augmented Fluorescence Imaging of Non-Small Cell Lung Cancer Protease Activity via a Dual-Enzyme Nanoprobe

Protease activity mapping plays a vital role in understanding tumor microenvironments and developing diagnostic tools. However, simultaneous quantification of multiple protease activities in complex biological systems remains challenging due to probe instability, signal overlap, and limited analytical throughput. Here, we present a dual-enzyme-responsive Au–Se nanoprobe functionalized with two orthogonally labeled peptide substrates for kallikrein 6 (KLK6) and urokinase-type plasminogen activator (uPA), two proteases implicated in nonsmall cell lung cancer (NSCLC). The use of gold–selenium bonds enhances resistance to glutathione-induced degradation and maintains fluorescence quenching stability in physiological conditions. To augment signal analysis, we integrate deep learning-based segmentation using Cellpose and U-Net to extract quantitative data from single-cell and in vivo imaging, respectively. This AI-assisted workflow significantly improved measurement reproducibility and enabled high-content quantification of protease activity distributions and tumor-to-background ratios, establishing a robust platform for dual-protease sensing in complex biological systems.

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Publication Details

Journal
Analytical Chemistry
Published
2026-06-30
DOI
https://doi.org/10.1021/acs.analchem.6c01259
Primary Topic
Nanoplatforms for cancer theranostics
Type
article
Field-Weighted Citation Impact
0.00

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article

AI-Augmented Fluorescence Imaging of Non-Small Cell Lung Cancer Protease Activity via a Dual-Enzyme Nanoprobe

Xiaonan Gao, Xi Zhang, Bo Tang, Yan He et al.
Analytical Chemistry
Nanoplatforms for cancer theranostics
article

AI-Augmented Fluorescence Imaging of Non-Small Cell Lung Cancer Protease Activity via a Dual-Enzyme Nanoprobe

Xiaonan Gao, Xi Zhang, Bo Tang, Yan He, Wenjun Cui, Chen Pang, Y J Tang, Jialin Chang, Lei Lyu
article en

Abstract

Protease activity mapping plays a vital role in understanding tumor microenvironments and developing diagnostic tools. However, simultaneous quantification of multiple protease activities in complex biological systems remains challenging due to probe instability, signal overlap, and limited analytical throughput. Here, we present a dual-enzyme-responsive Au–Se nanoprobe functionalized with two orthogonally labeled peptide substrates for kallikrein 6 (KLK6) and urokinase-type plasminogen activator (uPA), two proteases implicated in nonsmall cell lung cancer (NSCLC). The use of gold–selenium bonds enhances resistance to glutathione-induced degradation and maintains fluorescence quenching stability in physiological conditions. To augment signal analysis, we integrate deep learning-based segmentation using Cellpose and U-Net to extract quantitative data from single-cell and in vivo imaging, respectively. This AI-assisted workflow significantly improved measurement reproducibility and enabled high-content quantification of protease activity distributions and tumor-to-background ratios, establishing a robust platform for dual-protease sensing in complex biological systems.

Analytical Chemistry
Qingdao Binhai University (CN), Shandong Normal University (CN), Ministry of Education (ME), Qilu Hospital of Shandong University (CN)
National Natural Science Foundation of China, Natural Science Foundation of Shandong Province, Taishan Scholar Foundation of Shandong Province, Key Technology Research and Development Program of Shandong
Good health and well-being
Openalex Percentile: Top 13%
Nanoplatforms for cancer theranostics
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