Source:http://linkedlifedata.com/resource/pubmed/id/12963710
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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
48
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| pubmed:dateCreated |
2003-11-24
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| pubmed:abstractText |
Follicle-stimulating hormone (FSH) comprises an alpha subunit and a beta subunit, whereas the FSH receptor consists of two halves with distinct functions: the N-terminal extracellular exodomain and C-terminal membrane-associated endodomain. FSH initially binds to exodomain, and the resulting FSH/exodomain complex modulates the endodomain and generates signal. However, it has been difficult to determine which subunit of FSH contacts the exodomain or endodomain and in what orientation FSH interacts with them. To address these crucial issues, the receptor was Ala-scanned and the hormone subunits were probed with photoaffinity labeling with receptor peptides corresponding to the N-terminal region of the exodomain and exoloop 3 of the endodomain. Our results show that both regions of the receptors are important for hormone binding and signal generation. In addition, the FSH beta subunit is specifically labeled with the N-terminal peptide, whereas the alpha subunit is labeled with the exoloop 3 peptide. These contrasting results show that the FSH beta subunit is close to the N-terminal region and that the alpha subunit is projected toward exoloop 3 in the endodomain. The results raise the fundamental question whether the alpha subunit, common among the glycoprotein hormones, plays a major role in generating the hormone signal common to all glycoprotein hormones.
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| pubmed:grant | |
| pubmed:language |
eng
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| pubmed:journal | |
| pubmed:citationSubset |
IM
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| pubmed:chemical | |
| pubmed:status |
MEDLINE
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| pubmed:month |
Nov
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| pubmed:issn |
0021-9258
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| pubmed:author | |
| pubmed:issnType |
Print
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| pubmed:day |
28
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| pubmed:volume |
278
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| pubmed:owner |
NLM
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| pubmed:authorsComplete |
Y
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| pubmed:pagination |
47868-76
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| pubmed:dateRevised |
2007-11-14
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| pubmed:meshHeading |
pubmed-meshheading:12963710-Amino Acid Sequence,
pubmed-meshheading:12963710-Cell Line,
pubmed-meshheading:12963710-Crystallography, X-Ray,
pubmed-meshheading:12963710-Cyclic AMP,
pubmed-meshheading:12963710-Dose-Response Relationship, Drug,
pubmed-meshheading:12963710-Follicle Stimulating Hormone,
pubmed-meshheading:12963710-Glycoproteins,
pubmed-meshheading:12963710-Glycosylation,
pubmed-meshheading:12963710-Humans,
pubmed-meshheading:12963710-Immunoblotting,
pubmed-meshheading:12963710-Kinetics,
pubmed-meshheading:12963710-Light,
pubmed-meshheading:12963710-Models, Molecular,
pubmed-meshheading:12963710-Molecular Sequence Data,
pubmed-meshheading:12963710-Mutagenesis,
pubmed-meshheading:12963710-Peptides,
pubmed-meshheading:12963710-Protein Binding,
pubmed-meshheading:12963710-Protein Conformation,
pubmed-meshheading:12963710-Protein Structure, Secondary,
pubmed-meshheading:12963710-Protein Structure, Tertiary,
pubmed-meshheading:12963710-Sequence Homology, Amino Acid,
pubmed-meshheading:12963710-Transfection,
pubmed-meshheading:12963710-Ultraviolet Rays
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| pubmed:year |
2003
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| pubmed:articleTitle |
Orientation of follicle-stimulating hormone (FSH) subunits complexed with the FSH receptor. Beta subunit toward the N terminus of exodomain and alpha subunit to exoloop 3.
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| pubmed:affiliation |
Department of Chemistry, University of Kentucky, Lexington, Kentucky 40506-0055, USA.
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| pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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