Detection of Active Granzyme A in NK92 Cells with Fluorescent Activity-Based Probe.
Sonia KoltTomasz JaniszewskiDion KaisermanSylwia ModrzyckaScott J SnipasGuy SalvesenMarcin Dra GPhillip I BirdPaulina Kasperkiewicz-WasilewskaPublished in: Journal of medicinal chemistry (2020)
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.
Keyphrases
- cell cycle arrest
- cell death
- induced apoptosis
- nk cells
- quantum dots
- living cells
- natural killer cells
- endoplasmic reticulum stress
- cell therapy
- signaling pathway
- stem cells
- immune response
- dendritic cells
- peripheral blood
- label free
- cell proliferation
- amino acid
- oxidative stress
- mesenchymal stem cells
- anti inflammatory
- sensitive detection
- real time pcr