颗粒酶B
化学
颗粒酶
纳米笼
细胞生物学
重组DNA
组氨酸
免疫疗法
生物化学
细胞毒性T细胞
内化
细胞质
蛋白酶
肽
CTL公司*
半胱氨酸蛋白酶
半胱氨酸
抗体
内体
免疫系统
内吞作用
蛋白酵素
丝氨酸蛋白酶
氨基酸
癌症研究
肽序列
微泡
纳米载体
颗粒酶A
药物输送
细胞毒性
作者
Xueyan Hu,Qiqi Liu,Helong Kang,Ming Zhao,Zheng Zhou,Yuanke Li,Weicheng Peng,Tianyi Qi,Ruming Liu,Li Jiao,Jie Zhuang,Yijin Liu,Stephen Mann,Xinglu Huang
标识
DOI:10.1038/s41467-026-68773-x
摘要
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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