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- Publisher Website: 10.1002/pmic.201000039
- Scopus: eid_2-s2.0-77954732858
- PMID: 20512790
- WOS: WOS:000280615200015
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Article: Expanding the mouse embryonic stem cell proteome: Combining three proteomic approaches
Title | Expanding the mouse embryonic stem cell proteome: Combining three proteomic approaches |
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Authors | |
Keywords | 1-D gel electrophoresis 2-D chromatography Cell biology Embryonic stem cell Isoforms Shotgun proteomics |
Issue Date | 2010 |
Citation | Proteomics, 2010, v. 10 n. 14, p. 2728-2732 How to Cite? |
Abstract | The current study used three different proteomic strategies, which differed by their extent of intact protein separation, to examine the proteome of a pluripotent mouse embryonic stem cell line, R1. Proteins from whole-cell lysates were subjected either to 2-D-LC, or 1-DE, or were unfractionated prior to enzymatic digestion and subsequent analysis by MS. The results yielded 1895 identified non-redundant proteins and, for 128 of these, the specific isoform could be determined based on detection of an isoform-specific peptide. When compared with two previously published proteomic studies that used the same cell line, the current study reveals 612 new proteins. © 2010 Wiley-VCH Verlag GmbH & Co. KGaA. |
Persistent Identifier | http://hdl.handle.net/10722/195127 |
ISSN | 2023 Impact Factor: 3.4 2023 SCImago Journal Rankings: 1.011 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Gundry, RL | - |
dc.contributor.author | Tchernyshyov, I | - |
dc.contributor.author | Sheng, S | - |
dc.contributor.author | Tarasova, Y | - |
dc.contributor.author | Raginski, K | - |
dc.contributor.author | Boheler, KR | - |
dc.contributor.author | Van Eyk, JE | - |
dc.date.accessioned | 2014-02-25T01:40:12Z | - |
dc.date.available | 2014-02-25T01:40:12Z | - |
dc.date.issued | 2010 | - |
dc.identifier.citation | Proteomics, 2010, v. 10 n. 14, p. 2728-2732 | - |
dc.identifier.issn | 1615-9853 | - |
dc.identifier.uri | http://hdl.handle.net/10722/195127 | - |
dc.description.abstract | The current study used three different proteomic strategies, which differed by their extent of intact protein separation, to examine the proteome of a pluripotent mouse embryonic stem cell line, R1. Proteins from whole-cell lysates were subjected either to 2-D-LC, or 1-DE, or were unfractionated prior to enzymatic digestion and subsequent analysis by MS. The results yielded 1895 identified non-redundant proteins and, for 128 of these, the specific isoform could be determined based on detection of an isoform-specific peptide. When compared with two previously published proteomic studies that used the same cell line, the current study reveals 612 new proteins. © 2010 Wiley-VCH Verlag GmbH & Co. KGaA. | - |
dc.language | eng | - |
dc.relation.ispartof | Proteomics | - |
dc.subject | 1-D gel electrophoresis | - |
dc.subject | 2-D chromatography | - |
dc.subject | Cell biology | - |
dc.subject | Embryonic stem cell | - |
dc.subject | Isoforms | - |
dc.subject | Shotgun proteomics | - |
dc.title | Expanding the mouse embryonic stem cell proteome: Combining three proteomic approaches | - |
dc.type | Article | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1002/pmic.201000039 | - |
dc.identifier.pmid | 20512790 | - |
dc.identifier.scopus | eid_2-s2.0-77954732858 | - |
dc.identifier.volume | 10 | - |
dc.identifier.issue | 14 | - |
dc.identifier.spage | 2728 | - |
dc.identifier.epage | 2732 | - |
dc.identifier.isi | WOS:000280615200015 | - |
dc.identifier.issnl | 1615-9853 | - |