| Autor: |
Laczkó-Dobos H; Institute of Genetics, HUN-REN Biological Research Centre Szeged, Szeged, Hungary., Bhattacharjee A; Institute of Genetics, HUN-REN Biological Research Centre Szeged, Szeged, Hungary., Maddali AK; Institute of Genetics, HUN-REN Biological Research Centre Szeged, Szeged, Hungary.; Doctoral School of Biology, University of Szeged, Szeged, Hungary., Kincses A; Institute of Biophysics, HUN-REN Biological Research Centre Szeged, Szeged, Hungary., Abuammar H; Institute of Genetics, HUN-REN Biological Research Centre Szeged, Szeged, Hungary.; Doctoral School of Biology, University of Szeged, Szeged, Hungary., Sebők-Nagy K; Institute of Biophysics, HUN-REN Biological Research Centre Szeged, Szeged, Hungary., Páli T; Institute of Biophysics, HUN-REN Biological Research Centre Szeged, Szeged, Hungary., Dér A; Institute of Biophysics, HUN-REN Biological Research Centre Szeged, Szeged, Hungary., Hegedűs T; Department of Biophysics and Radiation Biology, Semmelweis University, Budapest, Hungary.; HUN-REN Biophysical Virology Research Group, Budapest, Hungary., Csordás G; Institute of Genetics, HUN-REN Biological Research Centre Szeged, Szeged, Hungary., Juhász G; Institute of Genetics, HUN-REN Biological Research Centre Szeged, Szeged, Hungary.; Department of Anatomy, Cell and Developmental Biology, Eötvös Loránd University, Budapest, Hungary. |
| Abstrakt: |
The autophagosomal SNARE STX17 (syntaxin 17) promotes lysosomal fusion and degradation, but its autophagosomal recruitment is incompletely understood. Notably, PtdIns4P is generated on autophagosomes and promotes fusion through an unknown mechanism. Here we show that soluble recombinant STX17 is spontaneously recruited to negatively charged liposomes and adding PtdIns4P to liposomes containing neutral lipids is sufficient for its recruitment. Consistently, STX17 colocalizes with PtdIns4P-positive autophagosomes in cells, and specific inhibition of PtdIns4P synthesis on autophagosomes prevents its loading. Molecular dynamics simulations indicate that C-terminal positively charged amino acids establish contact with membrane bilayers containing negatively charged PtdIns4P. Accordingly, Ala substitution of Lys and Arg residues in the C terminus of STX17 abolishes membrane binding and impairs its autophagosomal recruitment. Finally, only wild type but not Ala substituted STX17 expression rescues the autophagosome-lysosome fusion defect of STX17 loss-of-function cells. We thus identify a key step of autophagosome maturation that promotes lysosomal fusion. Abbreviations: Cardiolipin: 1',3'-bis[1-palmitoyl-2-oleoyl-sn-glycero-3-phospho]-glycerol; DMSO: dimethyl sulfoxide; GST: glutathione S-transferase; GUV: giant unilamellar vesicles; LAMP1: lysosomal associated membrane protein 1; MAP1LC3/LC3: microtubule associated protein 1 light chain 3; PA: 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphate; PC/POPC: 1-palmitoyl-2-oleoyl-glycero-3-phosphocholine; PG: 1-palmitoyl-2-linoleoyl-sn-glycero-3-phospho-(1'-rac-glycerol); PI: L-α-phosphatidylinositol; PI4K2A: phosphatidylinositol 4-kinase type 2 alpha; PIK3C3/VPS34: phosphatidylinositol 3-kinase catalytic subunit type 3; POPE/PE: 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphoethanolamine; PS: 1-stearoyl-2-linoleoyl-sn-glycero-3-phospho-L-serine; PtdIns(3,5)P 2 : 1,2-dioleoyl-sn-glycero-3-phospho-(1"-myo-inositol-3',5'-bisphosphate); PtdIns3P: 1,2- dioleoyl-sn-glycero-3-phospho-(1'-myo-inositol-3'-phosphate); PtdIns4P: 1,2-dioleoyl-sn-glycero-3-phospho-(1"-myo-inositol-4'-phosphate); SDS-PAGE: sodium dodecyl sulfate-polyacrylamide gel electrophoresis; STX17: syntaxin 17. |
