Granzyme B-mimetic nanozyme for nanovesicle targeted anticancer applications

Cytotoxic T lymphocytes play a crucial role in anti-tumour immunity, with granzyme B (GrB) being a decisive factor in this process. Developing a GrB-based delivery system to mimic T cell-based immunotherapy holds promise but remains challenging. Here, we present an artificial metalloenzyme (nanozyme) with GrB-like protease activity capable of inducing caspase-dependent cell apoptosis. The nanozyme is based on the site-specific binding of Pd(II) ions to recombinant human heavy chain apo-ferritin nanocages to generate a binuclear catalytic centre consisting of two Pd atoms with bridging cysteine ligands, monodentate methionine and histidine residues, and two water molecules. We show that encapsulation of the Pd-ferritin complex within membrane-fused lipid nanoparticles comprising surface-displayed single-chain antibodies affords GrB-mimicking nanozyme-based nanovesicles capable of receptor-mediated delivery of the nanozyme into the cytoplasm of tumour cells and induction of caspase-dependent apoptosis. This study provides valuable insights into the construction of nano-delivery systems with artificial GrB activity and presents a promising therapeutic option for solid tumours.

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Publication Details

Journal
Nature Communications
Published
2026-01-26
DOI
https://doi.org/10.1038/s41467-026-68773-x
Primary Topic
Advanced Nanomaterials in Catalysis
Type
article
Field-Weighted Citation Impact
0.00

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article

Granzyme B-mimetic nanozyme for nanovesicle targeted anticancer applications

Helong Kang, Yijin Liu, Xueyan Hu, Weicheng Peng et al.
Nature Communications
Advanced Nanomaterials in Catalysis
article

Granzyme B-mimetic nanozyme for nanovesicle targeted anticancer applications

Helong Kang, Yijin Liu, Xueyan Hu, Weicheng Peng, Tianyi Qi, Jie Zhuang, Ming Zhao, Yuanke Li, Ruming Liu, Qiqi Liu, Zheng Zhou, Xinglu Huang, Stephen Mann, Li Jiao
article en

Abstract

Cytotoxic T lymphocytes play a crucial role in anti-tumour immunity, with granzyme B (GrB) being a decisive factor in this process. Developing a GrB-based delivery system to mimic T cell-based immunotherapy holds promise but remains challenging. Here, we present an artificial metalloenzyme (nanozyme) with GrB-like protease activity capable of inducing caspase-dependent cell apoptosis. The nanozyme is based on the site-specific binding of Pd(II) ions to recombinant human heavy chain apo-ferritin nanocages to generate a binuclear catalytic centre consisting of two Pd atoms with bridging cysteine ligands, monodentate methionine and histidine residues, and two water molecules. We show that encapsulation of the Pd-ferritin complex within membrane-fused lipid nanoparticles comprising surface-displayed single-chain antibodies affords GrB-mimicking nanozyme-based nanovesicles capable of receptor-mediated delivery of the nanozyme into the cytoplasm of tumour cells and induction of caspase-dependent apoptosis. This study provides valuable insights into the construction of nano-delivery systems with artificial GrB activity and presents a promising therapeutic option for solid tumours.

Nature CommunicationsVol. 17(1)
Shanghai Jiao Tong University (CN), Nankai University (CN), At Bristol (GB), University of Bristol (GB)
National Natural Science Foundation of China
Openalex Percentile: Top 78%
Advanced Nanomaterials in Catalysis
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Granzyme B-mimetic nanozyme for nanovesicle targeted anticancer applications — Helong Kang, Yijin Liu, et al. · Nature Communications (2026) | TGRS Research Map | TGRS