Kołt Sonia, Janiszewski Tomasz, Kaiserman Dion, Modrzycka Sylwia, Snipas Scott J, Salvesen Guy, Dra G Marcin, Bird Phillip I, Kasperkiewicz Paulina
Wrocław University of Science and Technology, Department of Chemical Biology and Bioimaging, Wyb. Wyspiańskiego 29, 50-370 Wroclaw, Poland.
Monash University, Monash Biomedicine Discovery Institute, Department of Biochemistry and Molecular Biology, 23 Innovation Walk, Clayton, VIC 3800, Australia.
J Med Chem. 2020 Mar 26;63(6):3359-3369. doi: 10.1021/acs.jmedchem.9b02042. Epub 2020 Mar 16.
Cytotoxic T-lymphocytes (CTLs) and natural killer cells (NKs) kill compromised cells to defend against tumor and viral infections. Both effector cell types use multiple strategies to induce target cell death including Fas/CD95 activation and the release of perforin and a group of lymphocyte granule serine proteases called granzymes. Granzymes have relatively broad and overlapping substrate specificities and may hydrolyze a wide range of peptidic epitopes; it is therefore challenging to identify their natural and synthetic substrates and to distinguish their localization and functions. Here, we present a specific and potent substrate, an inhibitor, and an activity-based probe of Granzyme A (GrA) that can be used to follow functional GrA in cells.
细胞毒性T淋巴细胞(CTLs)和自然杀伤细胞(NKs)通过杀死受损细胞来抵御肿瘤和病毒感染。这两种效应细胞类型都使用多种策略诱导靶细胞死亡,包括Fas/CD95激活以及穿孔素和一组称为颗粒酶的淋巴细胞颗粒丝氨酸蛋白酶的释放。颗粒酶具有相对广泛且重叠的底物特异性,可能水解多种肽表位;因此,鉴定它们的天然和合成底物并区分它们的定位和功能具有挑战性。在这里,我们展示了一种颗粒酶A(GrA)的特异性强效底物、一种抑制剂和一种基于活性的探针,可用于追踪细胞中的功能性GrA。