| pubmed-article:12566452 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:12566452 | lifeskim:mentions | umls-concept:C0035334 | lld:lifeskim |
| pubmed-article:12566452 | lifeskim:mentions | umls-concept:C0443147 | lld:lifeskim |
| pubmed-article:12566452 | lifeskim:mentions | umls-concept:C0332281 | lld:lifeskim |
| pubmed-article:12566452 | lifeskim:mentions | umls-concept:C0596988 | lld:lifeskim |
| pubmed-article:12566452 | lifeskim:mentions | umls-concept:C0205464 | lld:lifeskim |
| pubmed-article:12566452 | lifeskim:mentions | umls-concept:C0185026 | lld:lifeskim |
| pubmed-article:12566452 | lifeskim:mentions | umls-concept:C1515655 | lld:lifeskim |
| pubmed-article:12566452 | pubmed:issue | 16 | lld:pubmed |
| pubmed-article:12566452 | pubmed:dateCreated | 2003-4-14 | lld:pubmed |
| pubmed-article:12566452 | pubmed:abstractText | Protein conformational disorders, which include certain types of retinitis pigmentosa, are a set of inherited human diseases in which mutant proteins are misfolded and often aggregated. Many opsin mutants associated with retinitis pigmentosa, the most common being P23H, are misfolded and retained within the cell. Here, we describe a pharmacological chaperone, 11-cis-7-ring retinal, that quantitatively induces the in vivo folding of P23H-opsin. The rescued protein forms pigment, acquires mature glycosylation, and is transported to the cell surface. Additionally, we determined the temperature stability of the rescued protein as well as the reactivity of the retinal-opsin Schiff base to hydroxylamine. Our study unveils novel properties of P23H-opsin and its interaction with the chromophore. These properties suggest that 11-cis-7-ring retinal may be a useful therapeutic agent for the rescue of P23H-opsin and the prevention of retinal degeneration. | lld:pubmed |
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| pubmed-article:12566452 | pubmed:language | eng | lld:pubmed |
| pubmed-article:12566452 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:12566452 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:12566452 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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| pubmed-article:12566452 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:12566452 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:12566452 | pubmed:month | Apr | lld:pubmed |
| pubmed-article:12566452 | pubmed:issn | 0021-9258 | lld:pubmed |
| pubmed-article:12566452 | pubmed:author | pubmed-author:PalczewskiKrz... | lld:pubmed |
| pubmed-article:12566452 | pubmed:author | pubmed-author:ImanishiYoshi... | lld:pubmed |
| pubmed-article:12566452 | pubmed:author | pubmed-author:FilipekSlawom... | lld:pubmed |
| pubmed-article:12566452 | pubmed:author | pubmed-author:LiZhuZ | lld:pubmed |
| pubmed-article:12566452 | pubmed:author | pubmed-author:KuksaVladimir... | lld:pubmed |
| pubmed-article:12566452 | pubmed:author | pubmed-author:NoorwezSyed... | lld:pubmed |
| pubmed-article:12566452 | pubmed:author | pubmed-author:KaushalShales... | lld:pubmed |
| pubmed-article:12566452 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:12566452 | pubmed:day | 18 | lld:pubmed |
| pubmed-article:12566452 | pubmed:volume | 278 | lld:pubmed |
| pubmed-article:12566452 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:12566452 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:12566452 | pubmed:pagination | 14442-50 | lld:pubmed |
| pubmed-article:12566452 | pubmed:dateRevised | 2010-12-3 | lld:pubmed |
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