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Structure paper

TitleStepwise gating of the Sec61 protein-conducting channel by Sec63 and Sec62.
Journal, issue, pagesNat Struct Mol Biol, Vol. 28, Issue 2, Page 162-172, Year 2021
Publish dateJan 4, 2021
AuthorsSamuel Itskanov / Katie M Kuo / James C Gumbart / Eunyong Park /
PubMed AbstractMany proteins are transported into the endoplasmic reticulum by the universally conserved Sec61 channel. Post-translational transport requires two additional proteins, Sec62 and Sec63, but their ...Many proteins are transported into the endoplasmic reticulum by the universally conserved Sec61 channel. Post-translational transport requires two additional proteins, Sec62 and Sec63, but their functions are poorly defined. In the present study, we determined cryo-electron microscopy (cryo-EM) structures of several variants of Sec61-Sec62-Sec63 complexes from Saccharomyces cerevisiae and Thermomyces lanuginosus and show that Sec62 and Sec63 induce opening of the Sec61 channel. Without Sec62, the translocation pore of Sec61 remains closed by the plug domain, rendering the channel inactive. We further show that the lateral gate of Sec61 must first be partially opened by interactions between Sec61 and Sec63 in cytosolic and luminal domains, a simultaneous disruption of which completely closes the channel. The structures and molecular dynamics simulations suggest that Sec62 may also prevent lipids from invading the channel through the open lateral gate. Our study shows how Sec63 and Sec62 work together in a hierarchical manner to activate Sec61 for post-translational protein translocation.
External linksNat Struct Mol Biol / PubMed:33398175 / PubMed Central
MethodsEM (single particle)
Resolution3.0 - 4.4 Å
Structure data

EMDB-22770, PDB-7kah:
Cryo-EM structure of the Sec complex from S. cerevisiae, wild-type, class without Sec62
Method: EM (single particle) / Resolution: 3.1 Å

EMDB-22771, PDB-7kai:
Cryo-EM structure of the Sec complex from S. cerevisiae, wild-type, class with Sec62, conformation 1 (C1)
Method: EM (single particle) / Resolution: 3.2 Å

EMDB-22772, PDB-7kaj:
Cryo-EM structure of the Sec complex from S. cerevisiae, wild-type, class with Sec62, conformation 2 (C2)
Method: EM (single particle) / Resolution: 3.1 Å

EMDB-22773, PDB-7kak:
Cryo-EM structure of the Sec complex from T. lanuginosus, wild-type, class without Sec62
Method: EM (single particle) / Resolution: 3.9 Å

EMDB-22774, PDB-7kal:
Cryo-EM structure of the Sec complex from T. lanuginosus, wild-type, class with Sec62, plug-open conformation
Method: EM (single particle) / Resolution: 4.0 Å

EMDB-22775, PDB-7kam:
Cryo-EM structure of the Sec complex from T. lanuginosus, wild-type, class with Sec62, plug-closed conformation
Method: EM (single particle) / Resolution: 3.8 Å

EMDB-22776: Cryo-EM structure of the Sec complex from T. lanuginosus lacking Sec62
PDB-7kan: Cryo-EM structure of the Sec complex from T. lanuginosus, Sec62-lacking mutant (Delta Sec62)
Method: EM (single particle) / Resolution: 3.7 Å

EMDB-22777:
Cryo-EM structure of the Sec complex from T. lanuginosus, Sec62 anchor domain mutant (delta anchor)
Method: EM (single particle) / Resolution: 4.4 Å

EMDB-22778, PDB-7kao:
Cryo-EM structure of the Sec complex from S. cerevisiae, Sec61 pore mutant, class without Sec62
Method: EM (single particle) / Resolution: 4.0 Å

EMDB-22779, PDB-7kap:
Cryo-EM structure of the Sec complex from S. cerevisiae, Sec61 pore mutant, class with Sec62, conformation 1 (C1)
Method: EM (single particle) / Resolution: 4.1 Å

EMDB-22780, PDB-7kaq:
Cryo-EM structure of the Sec complex from S. cerevisiae, Sec61 pore mutant, class with Sec62, conformation 2 (C2)
Method: EM (single particle) / Resolution: 4.0 Å

EMDB-22781, PDB-7kar:
Cryo-EM structure of the Sec complex from S. cerevisiae, Sec63 FN3 mutant, class without Sec62
Method: EM (single particle) / Resolution: 4.0 Å

EMDB-22782, PDB-7kas:
Cryo-EM structure of the Sec complex from S. cerevisiae, Sec63 FN3 mutant, class with Sec62
Method: EM (single particle) / Resolution: 3.9 Å

EMDB-22783, PDB-7kat:
Cryo-EM structure of the Sec complex from S. cerevisiae, Sec61 pore ring and Sec63 FN3 double mutant, class without Sec62
Method: EM (single particle) / Resolution: 4.4 Å

EMDB-22784, PDB-7kau:
Cryo-EM structure of the Sec complex from S. cerevisiae, Sec61 pore ring and Sec63 FN3 double mutant, class with Sec62
Method: EM (single particle) / Resolution: 4.0 Å

EMDB-22785:
Cryo-EM structure of the Sec complex from S. cerevisiae, wild-type, consensus map
Method: EM (single particle) / Resolution: 3.0 Å

EMDB-22786:
Cryo-EM structure of the Sec complex from T. lanuginosus, wild-type, consensus map of classes with Sec62
Method: EM (single particle) / Resolution: 3.75 Å

EMDB-22787, PDB-7kb5:
Cryo-EM structure of the Sec complex from yeast, Sec63 FN3 and residues 210-216 mutated
Method: EM (single particle) / Resolution: 3.8 Å

Chemicals

ChemComp-PC1:
1,2-DIACYL-SN-GLYCERO-3-PHOSPHOCHOLINE / phospholipid*YM

Source
  • saccharomyces cerevisiae (strain atcc 204508 / s288c) (yeast)
  • saccharomyces cerevisiae by4741 (yeast)
  • thermomyces lanuginosus (fungus)
KeywordsPROTEIN TRANSPORT / Sec61 / translocon / endoplasmic reticulum / protein translocation / Sec62 / Sec63 / channel

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