@article{e46a7aa503724f29b17ad7a95a4b9b4d,
title = "Retriever is a multiprotein complex for retromer-independent endosomal cargo recycling",
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 α 5 β 1 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.",
author = "McNally, {Kerrie E.} and Rebecca Faulkner and Florian Steinberg and Matthew Gallon and Rajesh Ghai and David Pim and Paul Langton and Neil Pearson and Danson, {Chris M.} and Heike N{\"a}gele and Morris, {Lindsey L.} and Amika Singla and Overlee, {Brittany L.} and Heesom, {Kate J.} and Richard Sessions and Lawrence Banks and Collins, {Brett M.} and Imre Berger and Billadeau, {Daniel D.} and Ezra Burstein and Cullen, {Peter J.}",
note = "Funding Information: We thank the Wolfson Bioimaging Facility at the University of Bristol and also the Life Imaging Center (LIC) of the University of Freiburg for their support. P.J.C. is supported by the Medical Research Council (MR/K018299/1 and MR/P018807/1) and the Wellcome Trust (089928 and 104568). Funding to B.M.C. from the Australian Research Council (ARC) (DP160101743) and National Health and Medical Research Council (NHMRC) (APP1058734) is acknowledged. The NIH (R01DK073639, R01DK107733) supported E.B. and (R01AI65474) D.D.B. L.B. gratefully acknowledges research support from the Associazione Italiana per la Ricerca sul Cancro. L.B. acknowledges research support from the Associazione Italiana per la Ricerca sul Cancro grant no. 18578. Wellcome Trust PhD Studentships from the Dynamic Cell Biology programme (083474) supported K.E.M. and M.G. An NHMRC Dementia Fellowship (APP1097185) supported R.G., and B.M.C. is supported by an NHMRC Career Development Fellowship (APP1061574). F.S. is funded by the German Research Council (DFG) Emmy Noether grant (STE2310/1-1). Publisher Copyright: {\textcopyright} 2017 Macmillan Publishers Limited, part of Springer Nature. All rights reserved.",
year = "2017",
month = sep,
day = "29",
doi = "10.1038/ncb3610",
language = "English (US)",
volume = "19",
pages = "1214--1225",
journal = "Nature Cell Biology",
issn = "1465-7392",
publisher = "Nature Publishing Group",
number = "10",
}