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pubmed-article:20386969pubmed:dateCreated2010-5-7lld:pubmed
pubmed-article:20386969pubmed:abstractTextDopachrome tautomerase (DCT) plays a critical role in lowering the oxidative stress resulting from melanogenesis. Levels of DCT are elevated in melanoma cell lines that are especially resistant to chemotherapy and radiation. DCT is processed as a melanoma antigen and is a potential target for immunotherapy. In order to establish a more complete understanding of the role that DCT may play in the etiology and treatment of melanoma skin cancer, isolation of highly pure and properly processed protein is necessary. Purification of native DCT has been problematic due to a hydrophobic transmembrane anchor and interactions with melanin. In this study, DCT was expressed, without its carboxy-terminal transmembrane region using an Sf9 insect cell protein expression system and its recombinant protein was purified by various chromatographic techniques. Analysis of DCT tryptic peptides by MALDI-TOF/TOF determined N-glycosylation as a primary post-translational modification. Our success in the expression of soluble mammalian DCT and the characterization of N-glycosylation sites is a useful reference toward the comprehensive understanding of the structure/function relationship of mammalian DCT.lld:pubmed
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pubmed-article:20386969pubmed:authorpubmed-author:LiJianyongJlld:pubmed
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pubmed-article:20386969pubmed:authorpubmed-author:RayKeith WKWlld:pubmed
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pubmed-article:20386969pubmed:volume29lld:pubmed
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pubmed-article:20386969pubmed:pagination204-12lld:pubmed
pubmed-article:20386969pubmed:dateRevised2011-1-4lld:pubmed
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pubmed-article:20386969pubmed:articleTitlePurification and N-glycosylation analysis of melanoma antigen dopachrome tautomerase.lld:pubmed
pubmed-article:20386969pubmed:affiliationDepartment of Biochemistry, Virginia Tech, 111 Engel Hall, West Campus Drive, Blacksburg, VA 24061, USA. cjv@vt.edulld:pubmed
pubmed-article:20386969pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:20386969pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
pubmed-article:20386969pubmed:publicationTypeResearch Support, N.I.H., Extramurallld:pubmed
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