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Mammalian Retromer Is an Adaptable Scaffold for Cargo Sorting from Endosomes.
Kendall, Amy K; Xie, Boyang; Xu, Peng; Wang, Jue; Burcham, Rodger; Frazier, Meredith N; Binshtein, Elad; Wei, Hui; Graham, Todd R; Nakagawa, Terunaga; Jackson, Lauren P.
Affiliation
  • Kendall AK; Department of Biological Sciences, Vanderbilt University, Nashville, TN 37232, USA; Center for Structural Biology, Vanderbilt University, Nashville, TN 37232, USA.
  • Xie B; Department of Biological Sciences, Vanderbilt University, Nashville, TN 37232, USA; Center for Structural Biology, Vanderbilt University, Nashville, TN 37232, USA.
  • Xu P; Department of Biological Sciences, Vanderbilt University, Nashville, TN 37232, USA.
  • Wang J; Center for Structural Biology, Vanderbilt University, Nashville, TN 37232, USA; Department of Biochemistry, Vanderbilt University, Nashville, TN 37205, USA.
  • Burcham R; Department of Biological Sciences, Vanderbilt University, Nashville, TN 37232, USA; Center for Structural Biology, Vanderbilt University, Nashville, TN 37232, USA.
  • Frazier MN; Department of Biological Sciences, Vanderbilt University, Nashville, TN 37232, USA; Center for Structural Biology, Vanderbilt University, Nashville, TN 37232, USA.
  • Binshtein E; Center for Structural Biology, Vanderbilt University, Nashville, TN 37232, USA.
  • Wei H; National Resource for Automated Molecular Microscopy, New York Structural Biology Center, New York, NY 10027, USA.
  • Graham TR; Department of Biological Sciences, Vanderbilt University, Nashville, TN 37232, USA.
  • Nakagawa T; Center for Structural Biology, Vanderbilt University, Nashville, TN 37232, USA; Department of Molecular Physiology & Biophysics, Vanderbilt University, Nashville, TN 37212, USA.
  • Jackson LP; Department of Biological Sciences, Vanderbilt University, Nashville, TN 37232, USA; Center for Structural Biology, Vanderbilt University, Nashville, TN 37232, USA; Department of Biochemistry, Vanderbilt University, Nashville, TN 37205, USA. Electronic address: lauren.p.jackson@vanderbilt.edu.
Structure ; 28(4): 393-405.e4, 2020 04 07.
Article in En | MEDLINE | ID: mdl-32027819
Metazoan retromer (VPS26/VPS35/VPS29) associates with sorting nexins on endosomal tubules to sort proteins to the trans-Golgi network or plasma membrane. Mechanisms of metazoan retromer assembly remain undefined. We combine single-particle cryoelectron microscopy with biophysical methods to uncover multiple oligomer structures. 2D class averages reveal mammalian heterotrimers; dimers of trimers; tetramers of trimers; and flat chains. These species are further supported by biophysical solution studies. We provide reconstructions of all species, including key sub-structures (∼5 Å resolution). Local resolution variation suggests that heterotrimers and dimers adopt multiple conformations. Our structures identify a flexible, highly conserved electrostatic dimeric interface formed by VPS35 subunits. We generate structure-based mutants to disrupt this interface in vitro. Equivalent mutations in yeast demonstrate a mild cargo-sorting defect. Our data suggest the metazoan retromer is an adaptable and plastic scaffold that accommodates interactions with different sorting nexins to sort multiple cargoes from endosomes their final destinations.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Endosomes / Vesicular Transport Proteins / Protein Multimerization Limits: Animals / Humans Language: En Journal: Structure Journal subject: BIOLOGIA MOLECULAR / BIOQUIMICA / BIOTECNOLOGIA Year: 2020 Document type: Article Affiliation country: Estados Unidos Country of publication: Estados Unidos

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Endosomes / Vesicular Transport Proteins / Protein Multimerization Limits: Animals / Humans Language: En Journal: Structure Journal subject: BIOLOGIA MOLECULAR / BIOQUIMICA / BIOTECNOLOGIA Year: 2020 Document type: Article Affiliation country: Estados Unidos Country of publication: Estados Unidos