颗粒酶
细胞毒性T细胞
颗粒酶A
免疫系统
颗粒酶B
穿孔素
抗原
细胞生物学
分泌物
化学
生物
获得性免疫系统
T细胞
免疫学
CD8型
生物化学
体外
作者
Zhiming Cheng,Emily Thompson,Lorena Mendive‐Tapia,Jamie I. Scott,Sam Benson,Takanori Kitamura,Ana Senan-Salinas,Youhani Samarakoon,Edward Roberts,Maykel Arias,Julián Pardo,Eva M. Gálvez,Marc Vendrell
标识
DOI:10.1002/anie.202216142
摘要
Cytotoxic immune cells, including T lymphocytes (CTLs) and natural killer (NK) cells, are essential components of the host response against tumors. CTLs and NK cells secrete granzyme A (GzmA) upon recognition of cancer cells; however, there are very few tools that can detect physiological levels of active GzmA with high spatiotemporal resolution. Herein, we report the rational design of the near-infrared fluorogenic substrates for human GzmA and mouse GzmA. These activity-based probes display very high catalytic efficiency and selectivity over other granzymes, as shown in tissue lysates from wild-type and GzmA knock-out mice. Furthermore, we demonstrate that the probes can image how adaptive immune cells respond to antigen-driven recognition of cancer cells in real time.
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