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Structure and function in rhodopsin: Mass spectrometric identification of the abnormal intradiscal disulfide bond in misfolded retinitis pigmentosa mutants

Retinitis pigmentosa (RP) point mutations in both the intradiscal (ID) and transmembrane domains of rhodopsin cause partial or complete misfolding of rhodopsin, resulting in loss of 11-cis-retinal binding. Previous work has shown that misfolding is caused by the formation of a disulfide bond in the...

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Autori principali: Hwa, John, Klein-Seetharaman, Judith, Khorana, H. Gobind
Natura: Artigo
Lingua:Inglês
Pubblicazione: The National Academy of Sciences 2001
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC33130/
https://ncbi.nlm.nih.gov/pubmed/11320236
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.061632798
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