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rdf:type |
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lifeskim:mentions |
umls-concept:C0017082,
umls-concept:C0034844,
umls-concept:C0332120,
umls-concept:C0439851,
umls-concept:C0449432,
umls-concept:C1179435,
umls-concept:C1524073,
umls-concept:C1548799,
umls-concept:C1552596,
umls-concept:C1705248,
umls-concept:C1947931
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pubmed:issue |
5
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pubmed:dateCreated |
1991-4-11
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pubmed:abstractText |
Gangliosides were extracted from purified human and porcine thyrotropin (TSH) receptors (TSH-R) and were detected by probing with an 125I-labeled sialic acid-specific lectin, Limax flavus agglutinin. Gangliosides copurified with human and porcine TSH-R migrated between monosialoganglioside GM1 and disialoganglioside GD1a. Ceramide glycanase digestion of the purified human TSH-R-associated glycolipid confirmed its ganglioside nature. It was resistant to Vibrio cholerae sialidase, which digests all gangliosides except GM1, but was sensitive to Arthrobacter ureafaciens sialidase, which digests all gangliosides including GM1. These findings indicate that the human TSH-R contains ganglioside that belongs to the galactosyl(beta 1----3)-N-acetylgalactosaminyl (beta 1----4)-[N-acetylneuraminyl(alpha 2----3)]galactosyl(beta 1----4) glucosyl(beta 1----1)ceramide (GM1) family. Its intimate association with receptor protein implies a key role for ganglioside in the structure and function of the TSH-R.
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pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/2000404-13436486,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2000404-17569488,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2000404-176657,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2000404-179095,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2000404-187196,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2000404-193492,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2000404-196600,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2000404-215191,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2000404-2302212,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2000404-2443507,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2000404-2471709,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2000404-2502842,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2000404-2502844,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2000404-2537177,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2000404-2556796,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2000404-2558651,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2000404-2673026,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2000404-2871067,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2000404-3527044,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2000404-3540954,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2000404-3668254,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2000404-3722160,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2000404-3801005,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2000404-3827921,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2000404-4005280,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2000404-4474010,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2000404-6088581,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2000404-6272516,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2000404-6301462,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2000404-6327695,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2000404-6762816,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2000404-7118850,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2000404-7381465,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2000404-942051
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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 |
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0027-8424
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:day |
1
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pubmed:volume |
88
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1991-5
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pubmed:dateRevised |
2009-11-18
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pubmed:meshHeading |
pubmed-meshheading:2000404-Adrenal Glands,
pubmed-meshheading:2000404-Amino Acid Sequence,
pubmed-meshheading:2000404-Animals,
pubmed-meshheading:2000404-Carbohydrate Sequence,
pubmed-meshheading:2000404-Cell Membrane,
pubmed-meshheading:2000404-Dogs,
pubmed-meshheading:2000404-Gangliosides,
pubmed-meshheading:2000404-Goiter, Nodular,
pubmed-meshheading:2000404-Graves Disease,
pubmed-meshheading:2000404-Humans,
pubmed-meshheading:2000404-Molecular Sequence Data,
pubmed-meshheading:2000404-Oligosaccharides,
pubmed-meshheading:2000404-Receptors, Thyrotropin,
pubmed-meshheading:2000404-Sequence Homology, Nucleic Acid,
pubmed-meshheading:2000404-Swine,
pubmed-meshheading:2000404-Thyroid Gland,
pubmed-meshheading:2000404-Thyrotropin
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pubmed:year |
1991
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pubmed:articleTitle |
Direct evidence that ganglioside is an integral component of the thyrotropin receptor.
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pubmed:affiliation |
Burnet Clinical Research Unit, Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia.
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, Non-U.S. Gov't
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