| pubmed-article:2196996 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:2196996 | lifeskim:mentions | umls-concept:C0019629 | lld:lifeskim |
| pubmed-article:2196996 | lifeskim:mentions | umls-concept:C1879748 | lld:lifeskim |
| pubmed-article:2196996 | lifeskim:mentions | umls-concept:C1706853 | lld:lifeskim |
| pubmed-article:2196996 | lifeskim:mentions | umls-concept:C1533691 | lld:lifeskim |
| pubmed-article:2196996 | lifeskim:mentions | umls-concept:C0936012 | lld:lifeskim |
| pubmed-article:2196996 | pubmed:issue | 2 | lld:pubmed |
| pubmed-article:2196996 | pubmed:dateCreated | 1990-8-30 | lld:pubmed |
| pubmed-article:2196996 | pubmed:abstractText | Recent evidence suggests that peptide ligands take part in the assembly of class I molecules in living cells. We now describe a simple system for studying class I assembly in vitro. Detergent extracts of the mutant cells RMA-S and .174, in which class I assembly does not occur spontaneously, will support assembly in vitro when specific peptides are added. Peptides stabilize a conformational change in the class I heavy chain and association with beta 2-microglobulin, at concentrations approximately 100-fold lower than required in "peptide feeding" experiments with whole cells. We show that peptides bind class I molecules during assembly and demonstrate that the conformational change induced in the heavy chain is influenced by the concentrations of both peptide and beta 2-microglobulin. | lld:pubmed |
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| pubmed-article:2196996 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:2196996 | pubmed:language | eng | lld:pubmed |
| pubmed-article:2196996 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:2196996 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:2196996 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:2196996 | pubmed:month | Jul | lld:pubmed |
| pubmed-article:2196996 | pubmed:issn | 0092-8674 | lld:pubmed |
| pubmed-article:2196996 | pubmed:author | pubmed-author:BarberBB | lld:pubmed |
| pubmed-article:2196996 | pubmed:author | pubmed-author:TownsendAA | lld:pubmed |
| pubmed-article:2196996 | pubmed:author | pubmed-author:FosterLL | lld:pubmed |
| pubmed-article:2196996 | pubmed:author | pubmed-author:TseAA | lld:pubmed |
| pubmed-article:2196996 | pubmed:author | pubmed-author:ElliottTT | lld:pubmed |
| pubmed-article:2196996 | pubmed:author | pubmed-author:CerundoloVV | lld:pubmed |
| pubmed-article:2196996 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:2196996 | pubmed:day | 27 | lld:pubmed |
| pubmed-article:2196996 | pubmed:volume | 62 | lld:pubmed |
| pubmed-article:2196996 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:2196996 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:2196996 | pubmed:pagination | 285-95 | lld:pubmed |
| pubmed-article:2196996 | pubmed:dateRevised | 2009-9-29 | lld:pubmed |
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| pubmed-article:2196996 | pubmed:year | 1990 | lld:pubmed |
| pubmed-article:2196996 | pubmed:articleTitle | Assembly of MHC class I molecules analyzed in vitro. | lld:pubmed |
| pubmed-article:2196996 | pubmed:affiliation | Institute of Molecular Medicine, John Radcliffe Hospital, Headington, Oxford, England. | lld:pubmed |
| pubmed-article:2196996 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:2196996 | pubmed:publicationType | In Vitro | lld:pubmed |
| pubmed-article:2196996 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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