| Literature DB >> 32027819 |
Amy K Kendall1, Boyang Xie1, Peng Xu2, Jue Wang3, Rodger Burcham1, Meredith N Frazier1, Elad Binshtein4, Hui Wei5, Todd R Graham2, Terunaga Nakagawa6, Lauren P Jackson7.
Abstract
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.Entities:
Keywords: cell biology; coat proteins; membrane trafficking; single-particle cryo-EM; structural biology
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Year: 2020 PMID: 32027819 PMCID: PMC7145723 DOI: 10.1016/j.str.2020.01.009
Source DB: PubMed Journal: Structure ISSN: 0969-2126 Impact factor: 5.006