pubmed-article:18413313 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:18413313 | lifeskim:mentions | umls-concept:C0020792 | lld:lifeskim |
pubmed-article:18413313 | lifeskim:mentions | umls-concept:C0332307 | lld:lifeskim |
pubmed-article:18413313 | lifeskim:mentions | umls-concept:C0338106 | lld:lifeskim |
pubmed-article:18413313 | lifeskim:mentions | umls-concept:C0205384 | lld:lifeskim |
pubmed-article:18413313 | lifeskim:mentions | umls-concept:C0022954 | lld:lifeskim |
pubmed-article:18413313 | lifeskim:mentions | umls-concept:C1524075 | lld:lifeskim |
pubmed-article:18413313 | lifeskim:mentions | umls-concept:C0599748 | lld:lifeskim |
pubmed-article:18413313 | lifeskim:mentions | umls-concept:C0936012 | lld:lifeskim |
pubmed-article:18413313 | lifeskim:mentions | umls-concept:C1561491 | lld:lifeskim |
pubmed-article:18413313 | lifeskim:mentions | umls-concept:C0337112 | lld:lifeskim |
pubmed-article:18413313 | pubmed:issue | 24 | lld:pubmed |
pubmed-article:18413313 | pubmed:dateCreated | 2008-6-9 | lld:pubmed |
pubmed-article:18413313 | pubmed:abstractText | Mammalian glycan chain elongation is mostly based on extending the type 2 chain, Galbeta1-4GlcNAc, whereas the corresponding type 1 chain, Galbeta1-3GlcNAc, is not normally extended. In a broader context of developing high sensitivity mass spectrometry methodologies for glycomic identification of Le(a) versus Le(x) and linear versus branched poly-N-acetyllactosamine (polyLacNAc), we have now shown that the dimeric type 1 glycan chain, as carried on the lactosylceramides of a human colonic adenocarcinoma cell line, Colo205, not only can be further extended linearly but can likewise be branched at C6 of 3-linked Gal in a manner similar to polyLacNAc. A combination of chemical and enzymatic derivatization coupled with advanced mass spectrometry analyses afforded unambiguous identification of a complex mixture of type 1 and 2 hybrids as well as those fucosylated variants founded exclusively on linear and branched trimeric type 1 chain. We further showed by in vitro enzymatic synthesis that extended type 1 and the hybrid chains can be branched by all three forms of the human I branching enzymes (IGnT) currently identified but with lower efficiency and stringency with respect to branching site preference. Importantly, it was found that a better substrate is one that carries a Gal site for branching that is extended at the non-reducing end by a type 2 and not a type 1 unit, whereas the IGnTs are less discriminative with respect to whether the targeted Gal site is itself beta3- or beta4-linked to GlcNAc at the reducing end. | lld:pubmed |
pubmed-article:18413313 | pubmed:language | eng | lld:pubmed |
pubmed-article:18413313 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18413313 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:18413313 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18413313 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18413313 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18413313 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18413313 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18413313 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:18413313 | pubmed:month | Jun | lld:pubmed |
pubmed-article:18413313 | pubmed:issn | 0021-9258 | lld:pubmed |
pubmed-article:18413313 | pubmed:author | pubmed-author:NarimatsuHisa... | lld:pubmed |
pubmed-article:18413313 | pubmed:author | pubmed-author:SatoTakashiT | lld:pubmed |
pubmed-article:18413313 | pubmed:author | pubmed-author:LinChi-HungCH | lld:pubmed |
pubmed-article:18413313 | pubmed:author | pubmed-author:KhooKay-HooiK... | lld:pubmed |
pubmed-article:18413313 | pubmed:author | pubmed-author:ItoHiromiH | lld:pubmed |
pubmed-article:18413313 | pubmed:author | pubmed-author:YuLung-ChihLC | lld:pubmed |
pubmed-article:18413313 | pubmed:author | pubmed-author:KameyamaAkihi... | lld:pubmed |
pubmed-article:18413313 | pubmed:author | pubmed-author:YuShin-YiSY | lld:pubmed |
pubmed-article:18413313 | pubmed:author | pubmed-author:FanYao-YunYY | lld:pubmed |
pubmed-article:18413313 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:18413313 | pubmed:day | 13 | lld:pubmed |
pubmed-article:18413313 | pubmed:volume | 283 | lld:pubmed |
pubmed-article:18413313 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:18413313 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:18413313 | pubmed:pagination | 16455-68 | lld:pubmed |
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pubmed-article:18413313 | pubmed:meshHeading | pubmed-meshheading:18413313... | lld:pubmed |
pubmed-article:18413313 | pubmed:year | 2008 | lld:pubmed |
pubmed-article:18413313 | pubmed:articleTitle | Identification of further elongation and branching of dimeric type 1 chain on lactosylceramides from colonic adenocarcinoma by tandem mass spectrometry sequencing analyses. | lld:pubmed |
pubmed-article:18413313 | pubmed:affiliation | Institute of Biochemical Sciences, National Taiwan University, Taipei 106, Taiwan. | lld:pubmed |
pubmed-article:18413313 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:18413313 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |