Expanding the mouse embryonic stem cell proteome: Combining three proteomic approaches

被引:17
作者
Gundry, Rebekah L. [1 ,2 ]
Tchernyshyov, Irina [1 ]
Sheng, Shijun [1 ]
Tarasova, Yelena [2 ]
Raginski, Kimberly [2 ]
Boheler, Kenneth R. [2 ]
Van Eyk, Jennifer E. [1 ,3 ,4 ]
机构
[1] Johns Hopkins Univ, Dept Med, Baltimore, MD 21224 USA
[2] NIA, NIH, Baltimore, MD 21224 USA
[3] Johns Hopkins Univ, Dept Biol Chem, Baltimore, MD 21224 USA
[4] Johns Hopkins Univ, Dept Biomed Engn, Baltimore, MD 21224 USA
关键词
1-D gel electrophoresis; 2-D chromatography; Cell biology; Embryonic stem cell; Isoforms; Shotgun proteomics; TRANSCRIPTIONAL NETWORK; STATISTICAL-MODEL; PLURIPOTENCY; DATABASE; IDENTIFICATIONS; PROTEINS;
D O I
10.1002/pmic.201000039
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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, Rl. 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.
引用
收藏
页码:2728 / 2732
页数:5
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