| Literature DB >> 19363302 |
Melanie Schwarten1, Jeannine Mohrlüder, Peixiang Ma, Matthias Stoldt, Yvonne Thielmann, Thomas Stangler, Nils Hersch, Bernd Hoffmann, Rudolf Merkel, Dieter Willbold.
Abstract
Autophagy, a pathway primarily relevant for cell survival, and apoptosis, a process invariably leading to cell death, are the two main mechanisms of cellular self-destruction, which are essential in cell growth, neurodegeneration, tumor suppression, stress and immune response. Currently, a potential crosstalk between apoptosis and autophagy is subject to intensive investigations since recently some direct junctions became obvious. The respective protein-protein interaction network, however, remains to be elucidated in detail. The gamma-aminobutyric acid type A (GABA(A)) receptor-associated protein GABARAP belongs to a family of proteins implicated in intracellular transport events and was shown to be associated to autophagic processes. Using a phage display screening against the target protein GABARAP, we identified the proapoptotic protein Nix/Bnip3L to be a potential GABARAP ligand. In vitro binding studies, pull-down analysis, coimmunoprecipitation assays and colocalization studies confirmed a direct interaction of both proteins in mammalian cells.Entities:
Mesh:
Substances:
Year: 2009 PMID: 19363302 DOI: 10.4161/auto.5.5.8494
Source DB: PubMed Journal: Autophagy ISSN: 1554-8627 Impact factor: 16.016