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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
18
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pubmed:dateCreated |
2002-4-29
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pubmed:abstractText |
The initial step of the intracellular transport of G protein-coupled receptors, their insertion into the membrane of the endoplasmic reticulum, follows one of two different pathways. Whereas one group uses the first transmembrane domain of the mature receptor as an uncleaved signal anchor sequence for this process, a second group possesses additional cleavable signal peptides. The reason this second subset requires the additional signal peptide is not known. Here we have assessed the functional significance of the signal peptide of the endothelin B (ET(B)) receptor in transiently transfected COS.M6 cells. A green fluorescent protein-tagged ET(B) receptor mutant lacking the signal peptide was nonfunctional and retained in the endoplasmic reticulum, suggesting that it has a folding defect. To determine the defect in more detail, ET(B) receptor fragments containing the N-terminal tail, first transmembrane domain, and first cytoplasmic loop were constructed. We assessed N tail translocation across the endoplasmic reticulum membrane in the presence and absence of a signal peptide and show that the signal peptide is necessary for N tail translocation. We postulate that signal peptides are necessary for those G protein-coupled receptors for which post-translational translocation of the N terminus is impaired or blocked by the presence of stably folded domains.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/DNA Primers,
http://linkedlifedata.com/resource/pubmed/chemical/Endothelin-1,
http://linkedlifedata.com/resource/pubmed/chemical/GTP-Binding Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Green Fluorescent Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Luminescent Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Protein Sorting Signals,
http://linkedlifedata.com/resource/pubmed/chemical/Receptor, Endothelin B,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Endothelin,
http://linkedlifedata.com/resource/pubmed/chemical/Recombinant Fusion Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Recombinant Proteins
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pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
0021-9258
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:day |
3
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pubmed:volume |
277
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
16131-8
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:11854280-Amino Acid Sequence,
pubmed-meshheading:11854280-Animals,
pubmed-meshheading:11854280-Base Sequence,
pubmed-meshheading:11854280-COS Cells,
pubmed-meshheading:11854280-Cercopithecus aethiops,
pubmed-meshheading:11854280-DNA Primers,
pubmed-meshheading:11854280-Endoplasmic Reticulum,
pubmed-meshheading:11854280-Endothelin-1,
pubmed-meshheading:11854280-GTP-Binding Proteins,
pubmed-meshheading:11854280-Green Fluorescent Proteins,
pubmed-meshheading:11854280-Humans,
pubmed-meshheading:11854280-Intracellular Membranes,
pubmed-meshheading:11854280-Kinetics,
pubmed-meshheading:11854280-Luminescent Proteins,
pubmed-meshheading:11854280-Models, Molecular,
pubmed-meshheading:11854280-Molecular Sequence Data,
pubmed-meshheading:11854280-Plasmids,
pubmed-meshheading:11854280-Polymerase Chain Reaction,
pubmed-meshheading:11854280-Protein Conformation,
pubmed-meshheading:11854280-Protein Sorting Signals,
pubmed-meshheading:11854280-Protein Transport,
pubmed-meshheading:11854280-Receptor, Endothelin B,
pubmed-meshheading:11854280-Receptors, Endothelin,
pubmed-meshheading:11854280-Recombinant Fusion Proteins,
pubmed-meshheading:11854280-Recombinant Proteins,
pubmed-meshheading:11854280-Transfection
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pubmed:year |
2002
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pubmed:articleTitle |
The signal peptide of the G protein-coupled human endothelin B receptor is necessary for translocation of the N-terminal tail across the endoplasmic reticulum membrane.
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pubmed:affiliation |
Forschungsinstitut für Molekulare Pharmakologie, Robert-Rössle-Strasse 10, 13125 Berlin, USA.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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