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Retriever is a multiprotein complex for retromer-independent endosomal cargo recycling.
McNally, Kerrie E; Faulkner, Rebecca; Steinberg, Florian; Gallon, Matthew; Ghai, Rajesh; Pim, David; Langton, Paul; Pearson, Neil; Danson, Chris M; Nägele, Heike; Morris, Lindsey L; Singla, Amika; Overlee, Brittany L; Heesom, Kate J; Sessions, Richard; Banks, Lawrence; Collins, Brett M; Berger, Imre; Billadeau, Daniel D; Burstein, Ezra; Cullen, Peter J.
Affiliation
  • McNally KE; School of Biochemistry, Biomedical Sciences Building, University of Bristol, Bristol BS8 1TD, UK.
  • Faulkner R; Department of Internal Medicine and Department of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA.
  • Steinberg F; Center for Biological Systems Analysis, Albert Ludwigs Universitaet Freiburg, 79104 Freiburg, Germany.
  • Gallon M; School of Biochemistry, Biomedical Sciences Building, University of Bristol, Bristol BS8 1TD, UK.
  • Ghai R; Institute for Molecular Bioscience, the University of Queensland, St. Lucia, Queensland 4072, Australia.
  • Pim D; International Centre for Genetic Engineering and Biotechnology, Padriciano 99, I-34149 Trieste, Italy.
  • Langton P; School of Biochemistry, Biomedical Sciences Building, University of Bristol, Bristol BS8 1TD, UK.
  • Pearson N; School of Biochemistry, Biomedical Sciences Building, University of Bristol, Bristol BS8 1TD, UK.
  • Danson CM; School of Biochemistry, Biomedical Sciences Building, University of Bristol, Bristol BS8 1TD, UK.
  • Nägele H; Center for Biological Systems Analysis, Albert Ludwigs Universitaet Freiburg, 79104 Freiburg, Germany.
  • Morris LL; Department of Internal Medicine and Department of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA.
  • Singla A; Department of Internal Medicine and Department of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA.
  • Overlee BL; Department of Biochemistry and Molecular Biology, and Department of Immunology, Mayo Clinic, Rochester, Minnesota 55905, USA.
  • Heesom KJ; Proteomics Facility, School of Biochemistry, University of Bristol, Bristol BS8 1TD, UK.
  • Sessions R; School of Biochemistry, Biomedical Sciences Building, University of Bristol, Bristol BS8 1TD, UK.
  • Banks L; International Centre for Genetic Engineering and Biotechnology, Padriciano 99, I-34149 Trieste, Italy.
  • Collins BM; Institute for Molecular Bioscience, the University of Queensland, St. Lucia, Queensland 4072, Australia.
  • Berger I; School of Biochemistry, Biomedical Sciences Building, University of Bristol, Bristol BS8 1TD, UK.
  • Billadeau DD; Department of Biochemistry and Molecular Biology, and Department of Immunology, Mayo Clinic, Rochester, Minnesota 55905, USA.
  • Burstein E; Department of Internal Medicine and Department of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA.
  • Cullen PJ; School of Biochemistry, Biomedical Sciences Building, University of Bristol, Bristol BS8 1TD, UK.
Nat Cell Biol ; 19(10): 1214-1225, 2017 Oct.
Article in En | MEDLINE | ID: mdl-28892079
ABSTRACT
Following endocytosis into the endosomal network, integral membrane proteins undergo sorting for lysosomal degradation or are retrieved and recycled back to the cell surface. Here we describe the discovery of an ancient and conserved multiprotein complex that orchestrates cargo retrieval and recycling and, importantly, is biochemically and functionally distinct from the established retromer pathway. We have called this complex 'retriever'; it is a heterotrimer composed of DSCR3, C16orf62 and VPS29, and bears striking similarity to retromer. We establish that retriever associates with the cargo adaptor sorting nexin 17 (SNX17) and couples to CCC (CCDC93, CCDC22, COMMD) and WASH complexes to prevent lysosomal degradation and promote cell surface recycling of α5ß1 integrin. Through quantitative proteomic analysis, we identify over 120 cell surface proteins, including numerous integrins, signalling receptors and solute transporters, that require SNX17-retriever to maintain their surface levels. Our identification of retriever establishes a major endosomal retrieval and recycling pathway.
Subject(s)

Full text: 1 Database: MEDLINE Main subject: Endosomes / Proteins / Cell Membrane / Vesicular Transport Proteins / Neoplasm Proteins Limits: Animals / Humans Language: En Year: 2017 Type: Article

Full text: 1 Database: MEDLINE Main subject: Endosomes / Proteins / Cell Membrane / Vesicular Transport Proteins / Neoplasm Proteins Limits: Animals / Humans Language: En Year: 2017 Type: Article