4.8 Article

Structure of the mitochondrial import gate reveals distinct preprotein paths

Journal

NATURE
Volume 575, Issue 7782, Pages 395-+

Publisher

NATURE RESEARCH
DOI: 10.1038/s41586-019-1680-7

Keywords

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Funding

  1. JSPS KAKENHI [15H05705, 2222703, 16K21680, 18K11543, 19K16077, 18KK0197, 26119003]
  2. JST CREST [JPMJCR12M1, JPMJCR14M1]
  3. European Research Council (ERC) [648235]
  4. Deutsche Forschungsgemeinschaft [BE 4679/2-2, PF 202/9-1]
  5. Germany's Excellence Strategy [390939984]
  6. Takeda Science Foundation
  7. Platform Project for Supporting Drug Discovery and Life Science Research (Basis for Supporting Innovative Drug Discovery and Life Science Research (BINDS)) from AMED [JP19am01011115, JP19am0101114]
  8. Ichiro Kanehara Foundation for the Promotion of Medical Sciences and Medical Care, Waksman Foundation of Japan, Tokyo Biochemical Research Foundation
  9. Sumitomo Foundation
  10. Naito Foundation
  11. Uehara Memorial Foundation
  12. Australian Research Council [DP160100227]
  13. Research Fellowship for Young Scientists from the Japan Society of the Promotion of Science [15J07687]
  14. Grants-in-Aid for Scientific Research [19K16077, 15J07687, 16K21680, 18K11543, 18KK0197, 26119003] Funding Source: KAKEN

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The translocase of the outer mitochondrial membrane (TOM) is the main entry gate for proteins(1-4). Here we use cryo-electron microscopy to report the structure of the yeast TOM core complex(5-9) at 3.8-angstrom resolution. The structure reveals the high-resolution architecture of the translocator consisting of two Tom40 beta-barrel channels and a-helical transmembrane subunits, providing insight into critical features that are conserved in all eukaryotes(1-3). Each Tom40 beta-barrel is surrounded by small TOM subunits, and tethered by two Tom22 subunits and one phospholipid. The N-terminal extension of Tom40 forms a helix inside the channel; mutational analysis reveals its dual role in early and late steps in the biogenesis of intermembrane-space proteins in cooperation with Tom5. Each Tom40 channel possesses two precursor exit sites. Tom22, Tom40 and Tom7 guide presequence-containing preproteins to the exit in the middle of the dimer, whereas Tom5 and the Tom40 N extension guide preproteins lacking a presequence to the exit at the periphery of the dimer.

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