The mechanism of tail-anchored protein insertion into the ER membrane.
Tail-anchored (TA) proteins access the secretory pathway via posttranslational insertion of their C-terminal transmembrane domain into the endoplasmic reticulum (ER). Get3 is an ATPase that delivers TA proteins to the ER by interacting with the Get1-Get2 transmembrane complex, but how Get3's nucleotide cycle drives TA protein insertion remains unclear. Here, ... we establish that nucleotide binding to Get3 promotes Get3-TA protein complex formation by recruiting Get3 to a chaperone that hands over TA proteins to Get3. Biochemical reconstitution and mutagenesis reveal that the Get1-Get2 complex comprises the minimal TA protein insertion machinery with functionally critical cytosolic regions. By engineering a soluble heterodimer of Get1-Get2 cytosolic domains, we uncover the mechanism of TA protein release from Get3: Get2 tethers Get3-TA protein complexes into proximity with the ATPase-dependent, substrate-releasing activity of Get1. Lastly, we show that ATP enhances Get3 dissociation from the membrane, thus freeing Get1-Get2 for new rounds of substrate insertion.
Mesh Terms:
Adaptor Proteins, Vesicular Transport, Adenosine Triphosphatases, Endoplasmic Reticulum, Guanine Nucleotide Exchange Factors, Liposomes, Membrane Proteins, Protein Transport, Saccharomyces cerevisiae, Saccharomyces cerevisiae Proteins
Adaptor Proteins, Vesicular Transport, Adenosine Triphosphatases, Endoplasmic Reticulum, Guanine Nucleotide Exchange Factors, Liposomes, Membrane Proteins, Protein Transport, Saccharomyces cerevisiae, Saccharomyces cerevisiae Proteins
Mol. Cell
Date: Sep. 02, 2011
PubMed ID: 21835666
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