Literature DB >> 24088629

Interaction of Pseudomonas aeruginosa Exotoxin A with the human Sec61 complex suppresses passive calcium efflux from the endoplasmic reticulum.

Nico Schäuble1, Adolfo Cavalié2, Richard Zimmermann1, Martin Jung1.   

Abstract

According to live-cell calcium-imaging experiments, the Sec61 complex is a passive calcium-leak channel in the human endoplasmic reticulum (ER) membrane that is regulated by ER luminal immunoglobulin heavy chain binding protein (BiP) and cytosolic Ca(2+)-calmodulin. In single channel measurements, the open Sec61 complex is Ca(2+) permeable. It can be closed not only by interaction with BiP or Ca(2+)-calmodulin, but also with Pseudomonas aeruginosa Exotoxin A which can enter human cells by retrograde transport. Exotoxin A has been shown to interact with the Sec61 complex and, thereby, inhibit ER export of immunogenic peptides into the cytosol. Here, we show that Exotoxin A also inhibits passive Ca(2+) leakage from the ER in human cells, and we characterized the N-terminus of the Sec61 α-subunit as the relevant binding site for Exotoxin A.

Entities:  

Keywords:  ER calcium leakage; Pseudomonas aeruginosa Exotoxin A; Sec61 complex; calcium homeostasis; endoplasmic reticulum

Mesh:

Substances:

Year:  2013        PMID: 24088629      PMCID: PMC4048345          DOI: 10.4161/chan.26526

Source DB:  PubMed          Journal:  Channels (Austin)        ISSN: 1933-6950            Impact factor:   3.493


  19 in total

1.  Reaction diffusion modeling of calcium dynamics with realistic ER geometry.

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2.  Peptide arrays on cellulose support: SPOT synthesis, a time and cost efficient method for synthesis of large numbers of peptides in a parallel and addressable fashion.

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3.  BiP mutants that are unable to interact with endoplasmic reticulum DnaJ proteins provide insights into interdomain interactions in BiP.

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4.  Different effects of Sec61α, Sec62 and Sec63 depletion on transport of polypeptides into the endoplasmic reticulum of mammalian cells.

Authors:  Sven Lang; Julia Benedix; Sorin V Fedeles; Stefan Schorr; Claudia Schirra; Nico Schäuble; Carolin Jalal; Markus Greiner; Sarah Hassdenteufel; Jörg Tatzelt; Birgit Kreutzer; Ludwig Edelmann; Elmar Krause; Jens Rettig; Stefan Somlo; Richard Zimmermann; Johanna Dudek
Journal:  J Cell Sci       Date:  2012-02-28       Impact factor: 5.285

5.  Sec61 complexes form ubiquitous ER Ca2+ leak channels.

Authors:  Sven Lang; Frank Erdmann; Martin Jung; Richard Wagner; Adolfo Cavalie; Richard Zimmermann
Journal:  Channels (Austin)       Date:  2011-05-01       Impact factor: 2.581

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Authors:  J E Wedekind; C B Trame; M Dorywalska; P Koehl; T M Raschke; M McKee; D FitzGerald; R J Collier; D B McKay
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8.  Live cell calcium imaging combined with siRNA mediated gene silencing identifies Ca²⁺ leak channels in the ER membrane and their regulatory mechanisms.

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10.  Expression and secretion of the cloned Pseudomonas aeruginosa exotoxin A by Escherichia coli.

Authors:  S Lory; M S Strom; K Johnson
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  12 in total

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Review 3.  Complexity and Specificity of Sec61-Channelopathies: Human Diseases Affecting Gating of the Sec61 Complex.

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5.  Eeyarestatin Compounds Selectively Enhance Sec61-Mediated Ca2+ Leakage from the Endoplasmic Reticulum.

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6.  Amino Acids 563-566 of the Na+/H+ Exchanger Isoform 1 C-Terminal Cytosolic Tail Prevent Protein Degradation and Stabilize Protein Expression and Activity.

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7.  Amino Acids 785, 787 of the Na+/H+ Exchanger Cytoplasmic Tail Modulate Protein Activity and Tail Conformation.

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8.  Toxin instability and its role in toxin translocation from the endoplasmic reticulum to the cytosol.

Authors:  Ken Teter
Journal:  Biomolecules       Date:  2013-12-10

Review 9.  Let's talk about Secs: Sec61, Sec62 and Sec63 in signal transduction, oncology and personalized medicine.

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Journal:  Signal Transduct Target Ther       Date:  2017-04-28

Review 10.  The signal peptide as a new target for drug design.

Authors:  Liezel A Lumangtad; Thomas W Bell
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