| pubmed-article:11680897 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:11680897 | lifeskim:mentions | umls-concept:C0237868 | lld:lifeskim |
| pubmed-article:11680897 | lifeskim:mentions | umls-concept:C0872252 | lld:lifeskim |
| pubmed-article:11680897 | lifeskim:mentions | umls-concept:C0936012 | lld:lifeskim |
| pubmed-article:11680897 | lifeskim:mentions | umls-concept:C0678632 | lld:lifeskim |
| pubmed-article:11680897 | pubmed:issue | 1 | lld:pubmed |
| pubmed-article:11680897 | pubmed:dateCreated | 2001-10-29 | lld:pubmed |
| pubmed-article:11680897 | pubmed:abstractText | Current methods of proteome analysis rely almost solely on two-dimensional polyacrylamide gel electrophoresis (2-D PAGE) followed by the excision of individual spots and protein identification using mass spectrometry (MS) and database searching. 2-D PAGE is denaturing in both dimensions and, thus, cannot indicate functional associations between individual proteins. Moreover, less abundant proteins are difficult to identify. To simplify the proteome, and explore functional associations, nondenaturing anion exchange column chromatography was used to separate a soluble protein extract from Escherichia coli. Successive fractions were then analysed using 2-D PAGE and selected spots from both the gels for the start material and the fractionated material were quantified and identified by peptide mass fingerprinting using a MALDI-TOF mass spectrometer. Enrichments of up to 13-fold were attained for individual protein spots and peptide mass fingerprints were of significantly higher quality after chromatographic separation. The marked anomalies between predicted p/and column elution position contrasted with the almost perfect correlation with migration distance on isoelectric focusing (IEF) and were explored further for basic proteins. | lld:pubmed |
| pubmed-article:11680897 | pubmed:language | eng | lld:pubmed |
| pubmed-article:11680897 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:11680897 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:11680897 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:11680897 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:11680897 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:11680897 | pubmed:month | Jan | lld:pubmed |
| pubmed-article:11680897 | pubmed:issn | 1615-9853 | lld:pubmed |
| pubmed-article:11680897 | pubmed:author | pubmed-author:SmithG JGJ | lld:pubmed |
| pubmed-article:11680897 | pubmed:author | pubmed-author:BeynonR JRJ | lld:pubmed |
| pubmed-article:11680897 | pubmed:author | pubmed-author:GaskellS JSJ | lld:pubmed |
| pubmed-article:11680897 | pubmed:author | pubmed-author:YoungJ AJA | lld:pubmed |
| pubmed-article:11680897 | pubmed:author | pubmed-author:OliverS GSG | lld:pubmed |
| pubmed-article:11680897 | pubmed:author | pubmed-author:ButtAA | lld:pubmed |
| pubmed-article:11680897 | pubmed:author | pubmed-author:DavisonM DMD | lld:pubmed |
| pubmed-article:11680897 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:11680897 | pubmed:volume | 1 | lld:pubmed |
| pubmed-article:11680897 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:11680897 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:11680897 | pubmed:pagination | 42-53 | lld:pubmed |
| pubmed-article:11680897 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
| pubmed-article:11680897 | pubmed:meshHeading | pubmed-meshheading:11680897... | lld:pubmed |
| pubmed-article:11680897 | pubmed:meshHeading | pubmed-meshheading:11680897... | lld:pubmed |
| pubmed-article:11680897 | pubmed:meshHeading | pubmed-meshheading:11680897... | lld:pubmed |
| pubmed-article:11680897 | pubmed:meshHeading | pubmed-meshheading:11680897... | lld:pubmed |
| pubmed-article:11680897 | pubmed:meshHeading | pubmed-meshheading:11680897... | lld:pubmed |
| pubmed-article:11680897 | pubmed:meshHeading | pubmed-meshheading:11680897... | lld:pubmed |
| pubmed-article:11680897 | pubmed:meshHeading | pubmed-meshheading:11680897... | lld:pubmed |
| pubmed-article:11680897 | pubmed:meshHeading | pubmed-meshheading:11680897... | lld:pubmed |
| pubmed-article:11680897 | pubmed:year | 2001 | lld:pubmed |
| pubmed-article:11680897 | pubmed:articleTitle | Chromatographic separations as a prelude to two-dimensional electrophoresis in proteomics analysis. | lld:pubmed |
| pubmed-article:11680897 | pubmed:affiliation | Department of Biomolecular Sciences, UMIST, School of Biological Sciences, University of Manchester, Manchester, UK. | lld:pubmed |
| pubmed-article:11680897 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:11680897 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:11680897 | lld:pubmed |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:11680897 | lld:pubmed |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:11680897 | lld:pubmed |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:11680897 | lld:pubmed |
