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AbstractAbstract
[en] The composition and structure of the complex oligosaccharides of thyrotropin (TSH) and free alpha-subunits are not well established, but are believed to be important determinants of the biological properties of these glycoproteins. We employed a simple double-label technique to learn the relative fucose content of mouse thyrotropin and free alpha-subunits. Thyrotropic tumor minces were incubated simultaneously with [35S]methionine and [3H]fucose. Thyrotropin and free alpha-subunits were labeled with both isotopes, and the ratio of 3H/35S was higher in free alpha-subunits than in thyrotropin; free alpha-subunits were approximately fivefold richer in fucose than was thyrotropin. The 3H/35S ratio was not substantially altered in TSH or free alpha-subunits secreted after a brief incubation with 10(-7) M thyrotropin-releasing hormone. Species which incorporated [3H]fucose were resistant to endoglycosidase H. Thus, mouse free alpha-subunits secreted by thyrotropic tumor are relatively rich in fucose. Double-isotope labeling using an amino acid and a sugar appears to be a useful technique for studies of the glycoprotein hormones
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Journal Article
Journal
Proceedings of the Society for Experimental Biology and Medicine; ISSN 0037-9727; ; CODEN PSEBA; (no.2); p. 237-240
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ANIMALS, BETA DECAY RADIOISOTOPES, BETA-MINUS DECAY RADIOISOTOPES, CARBOHYDRATES, DAYS LIVING RADIOISOTOPES, EVEN-ODD NUCLEI, HORMONES, HYDROGEN COMPOUNDS, ISOTOPE APPLICATIONS, ISOTOPES, LABELLING, LIGHT NUCLEI, MAMMALS, MONOSACCHARIDES, NUCLEI, ORGANIC COMPOUNDS, PEPTIDE HORMONES, PITUITARY HORMONES, RADIOISOTOPES, RODENTS, SACCHARIDES, SULFUR ISOTOPES, VERTEBRATES
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