Literature DB >> 10611978

The translocon: a dynamic gateway at the ER membrane.

A E Johnson1, M A van Waes.   

Abstract

Cotranslational protein translocation across and integration into the membrane of the endoplasmic reticulum (ER) occur at sites termed translocons. Translocons are composed of several ER membrane proteins that associate to form an aqueous pore through which secretory proteins and lumenal domains of membrane proteins pass from the cytoplasm to the ER lumen. These sites are not passive holes in the bilayer, but instead are quite dynamic both structurally and functionally. Translocons cycle between ribosome-bound and ribosome-free states, and convert between translocation and integration modes of operation. These changes in functional state are accompanied by structural rearrangements that alter translocon conformation, composition, and interactions with ligands such as the ribosome and BiP. Recent studies have revealed that the translocon is a complex and sophisticated molecular machine that regulates the movement of polypeptides through the bilayer, apparently in both directions as well as laterally into the bilayer, all while maintaining the membrane permeability barrier.

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Year:  1999        PMID: 10611978     DOI: 10.1146/annurev.cellbio.15.1.799

Source DB:  PubMed          Journal:  Annu Rev Cell Dev Biol        ISSN: 1081-0706            Impact factor:   13.827


  167 in total

1.  An essential amino acid residue in the protein translocation channel revealed by targeted random mutagenesis of SecY.

Authors:  H Mori; K Ito
Journal:  Proc Natl Acad Sci U S A       Date:  2001-04-17       Impact factor: 11.205

2.  Cross-talk between catalytic and regulatory elements in a DEAD motor domain is essential for SecA function.

Authors:  G Sianidis; S Karamanou; E Vrontou; K Boulias; K Repanas; N Kyrpides; A S Politou; A Economou
Journal:  EMBO J       Date:  2001-03-01       Impact factor: 11.598

3.  Sec63p and Kar2p are required for the translocation of SRP-dependent precursors into the yeast endoplasmic reticulum in vivo.

Authors:  B P Young; R A Craven; P J Reid; M Willer; C J Stirling
Journal:  EMBO J       Date:  2001-01-15       Impact factor: 11.598

4.  Location of a constriction in the lumen of a transmembrane pore by targeted covalent attachment of polymer molecules.

Authors:  L Movileanu; S Cheley; S Howorka; O Braha; H Bayley
Journal:  J Gen Physiol       Date:  2001-03       Impact factor: 4.086

5.  Proteins of the endoplasmic-reticulum-associated degradation pathway: domain detection and function prediction.

Authors:  C P Ponting
Journal:  Biochem J       Date:  2000-10-15       Impact factor: 3.857

6.  SRP-dependent co-translational targeting and SecA-dependent translocation analyzed as individual steps in the export of a bacterial protein.

Authors:  C Neumann-Haefelin; U Schäfer; M Müller; H G Koch
Journal:  EMBO J       Date:  2000-12-01       Impact factor: 11.598

7.  Identification of a membrane targeting and degradation signal in the p42 protein of influenza C virus.

Authors:  A Pekosz; R A Lamb
Journal:  J Virol       Date:  2000-11       Impact factor: 5.103

8.  The central cytoplasmic loop of the major facilitator superfamily of transport proteins governs efficient membrane insertion.

Authors:  A B Weinglass; H R Kaback
Journal:  Proc Natl Acad Sci U S A       Date:  2000-08-01       Impact factor: 11.205

9.  Visualization of the ER-to-cytosol dislocation reaction of a type I membrane protein.

Authors:  Edda Fiebiger; Craig Story; Hidde L Ploegh; Domenico Tortorella
Journal:  EMBO J       Date:  2002-03-01       Impact factor: 11.598

10.  Translocation of a functional protein by a voltage-dependent ion channel.

Authors:  Stephen L Slatin; Angèle Nardi; Karen S Jakes; Daniel Baty; Denis Duché
Journal:  Proc Natl Acad Sci U S A       Date:  2002-02-05       Impact factor: 11.205

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