Structural basis for Rab6 activation by the Ric1-Rgp1 complex

被引:1
作者
Feathers, J. Ryan [1 ,2 ,3 ]
Vignogna, Ryan C. [1 ,2 ]
Fromme, J. Christopher [1 ,2 ]
机构
[1] Cornell Univ, Dept Mol Biol & Genet, Ithaca, NY 14850 USA
[2] Cornell Univ, Weill Inst Cell & Mol Biol, Ithaca, NY 14850 USA
[3] Princeton Univ, 201 Schultz Lab, Princeton, NJ 08544 USA
关键词
GUANINE-NUCLEOTIDE-EXCHANGE; GTP-BINDING PROTEINS; C-TERMINAL DOMAIN; CRYO-EM; SACCHAROMYCES-CEREVISIAE; GTPASES; MECHANISM; VESICLES; EFFECTOR; INSIGHTS;
D O I
10.1038/s41467-024-54869-9
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Rab GTPases act as molecular switches to regulate organelle homeostasis and membrane trafficking. Rab6 plays a central role in regulating cargo flux through the Golgi and is activated via nucleotide exchange by the Ric1-Rgp1 protein complex. Ric1-Rgp1 is conserved throughout eukaryotes but the structural and mechanistic basis for its function has not been established. Here we report the cryoEM structure of a Ric1-Rgp1-Rab6 complex representing a key intermediate of the nucleotide exchange reaction. Ric1-Rgp1 interacts with the nucleotide-binding domain of Rab6 using an uncharacterized helical domain, which we establish as a RabGEF domain by identifying residues required for Rab6 activation. Unexpectedly, the complex uses an arrestin fold to interact with the Rab6 hypervariable domain, indicating that interactions with the unstructured C-terminal regions of Rab GTPases may be a common binding mechanism used by their activators. Collectively, our findings provide a detailed mechanistic understanding of regulated Rab6 activation at the Golgi.
引用
收藏
页数:13
相关论文
共 83 条
  • [1] New tools for the analysis and validation of cryo-EM maps and atomic models
    Afonine, Pavel V.
    Klaholz, Bruno P.
    Moriarty, Nigel W.
    Poon, Billy K.
    Sobolev, Oleg V.
    Terwilliger, Thomas C.
    Adams, Paul D.
    Urzhumtsev, Alexandre
    [J]. ACTA CRYSTALLOGRAPHICA SECTION D-STRUCTURAL BIOLOGY, 2018, 74 : 814 - 840
  • [2] Real-space refinement in PHENIX for cryo-EM and crystallography
    Afonine, Pavel V.
    Poon, Billy K.
    Read, Randy J.
    Sobolev, Oleg V.
    Terwilliger, Thomas C.
    Urzhumtsev, Alexandre
    Adams, Paul D.
    [J]. ACTA CRYSTALLOGRAPHICA SECTION D-STRUCTURAL BIOLOGY, 2018, 74 : 531 - 544
  • [3] Multiple regions contribute to membrane targeting of Rab GTPases
    Ali, BR
    Wasmeier, C
    Lamoreux, L
    Strom, M
    Seabra, MC
    [J]. JOURNAL OF CELL SCIENCE, 2004, 117 (26) : 6401 - 6412
  • [4] Rab6 promotes insulin receptor and cathepsin trafficking to regulate autophagy induction and activity in Drosophila
    Ayala, Carlos I.
    Kim, Jung
    Neufeld, Thomas P.
    [J]. JOURNAL OF CELL SCIENCE, 2018, 131 (17)
  • [5] The TRAPP complexes: discriminating GTPases in context
    Bagde, Saket R.
    Fromme, J. Christopher
    [J]. FEBS LETTERS, 2023, 597 (06) : 721 - 733
  • [6] Structure of a TRAPPII-Rab11 activation intermediate reveals GTPase substrate selection mechanisms
    Bagde, Saket R.
    Fromme, J. Christopher
    [J]. SCIENCE ADVANCES, 2022, 8 (19)
  • [7] Phenotypic characterisation of RAB6A knockout mouse embryonic fibroblasts
    Bardin, Sabine
    Miserey-Lenkei, Stephanie
    Hurbain, Ilse
    Garcia-Castillo, Daniela
    Raposo, Graca
    Goud, Bruno
    [J]. BIOLOGY OF THE CELL, 2015, 107 (12) : 427 - 439
  • [8] Rab GTPases and membrane identity: Causal or inconsequential?
    Barr, Francis A.
    [J]. JOURNAL OF CELL BIOLOGY, 2013, 202 (02) : 191 - 199
  • [9] THE EFFECTOR DOMAIN OF RAB6, PLUS A HIGHLY HYDROPHOBIC-C TERMINUS, IS REQUIRED FOR GOLGI-APPARATUS LOCALIZATION
    BERANGER, F
    PATERSON, H
    POWERS, S
    DEGUNZBURG, J
    HANCOCK, JF
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (01) : 744 - 758
  • [10] BERANGER F, 1994, J BIOL CHEM, V269, P13637