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Retromer-mediated endosomal protein sorting: The role of unstructured domains.
Mukadam, Aamir S; Seaman, Matthew N J.
Affiliation
  • Mukadam AS; Cambridge Institute for Medical Research, Dept. of Clinical Biochemistry, University of Cambridge, Wellcome Trust/MRC Building, Addenbrookes Hospital, Cambridge CB2 0XY, United Kingdom.
  • Seaman MN; Cambridge Institute for Medical Research, Dept. of Clinical Biochemistry, University of Cambridge, Wellcome Trust/MRC Building, Addenbrookes Hospital, Cambridge CB2 0XY, United Kingdom. Electronic address: mnjs100@cam.ac.uk.
FEBS Lett ; 589(19 Pt A): 2620-6, 2015 Sep 14.
Article in En | MEDLINE | ID: mdl-26072290
ABSTRACT
The retromer complex is a key element of the endosomal protein sorting machinery that is conserved through evolution and has been shown to play a role in diseases such as Alzheimer's disease and Parkinson's disease. Through sorting various membrane proteins (cargo), the function of retromer complex has been linked to physiological processes such as lysosome biogenesis, autophagy, down regulation of signalling receptors and cell spreading. The cargo-selective trimer of retromer recognises membrane proteins and sorts them into two distinct pathways; endosome-to-Golgi retrieval and endosome-to-cell surface recycling and additionally the cargo-selective trimer functions as a hub to recruit accessory proteins to endosomes where they may regulate and/or facilitate retromer-mediated endosomal proteins sorting. Unstructured domains present in cargo proteins or accessory factors play key roles in both these aspects of retromer function and will be discussed in this review.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Endosomes / Multiprotein Complexes / Golgi Apparatus / Membrane Proteins Type of study: Prognostic_studies Limits: Animals / Humans Language: En Journal: FEBS Lett Year: 2015 Document type: Article Affiliation country: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Endosomes / Multiprotein Complexes / Golgi Apparatus / Membrane Proteins Type of study: Prognostic_studies Limits: Animals / Humans Language: En Journal: FEBS Lett Year: 2015 Document type: Article Affiliation country: United kingdom