TY - JOUR
T1 - Detection of Active Granzyme A in NK92 Cells with Fluorescent Activity-Based Probe
AU - Kołt, Sonia
AU - Janiszewski, Tomasz
AU - Kaiserman, Dion
AU - Modrzycka, Sylwia
AU - Snipas, Scott J.
AU - Salvesen, Guy
AU - Dra¸g, Marcin
AU - Bird, Phillip I.
AU - Kasperkiewicz, Paulina
PY - 2020/3/26
Y1 - 2020/3/26
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85082542531&partnerID=8YFLogxK
U2 - 10.1021/acs.jmedchem.9b02042
DO - 10.1021/acs.jmedchem.9b02042
M3 - Article
C2 - 32142286
AN - SCOPUS:85082542531
SN - 0022-2623
VL - 63
SP - 3359
EP - 3369
JO - Journal of Medicinal Chemistry
JF - Journal of Medicinal Chemistry
IS - 6
ER -