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 J. Thompson,Lorena Mendive‐Tapia,Jamie I. Scott,Sam Benson,Takanori Kitamura,Ana Senan‐Salinas,Youhani Samarakoon,Edward W. 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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