Toward a protein profile of Escherichia coli:: Comparison to its transcription profile

被引:140
作者
Corbin, RW
Paliy, O
Yang, F
Shabanowitz, J
Platt, M
Lyons, CE
Root, K
McAuliffe, J
Jordan, MI
Kustu, S
Soupene, E
Hunt, DF
机构
[1] Univ Calif Berkeley, Dept Plant & Microbial Biol, Berkeley, CA 94720 USA
[2] Univ Virginia, Dept Chem, Charlottesville, VA 22901 USA
关键词
D O I
10.1073/pnas.1533294100
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
High-pressure liquid chromatography-tandem mass spectrometry was used to obtain a protein profile of Escherichia coli strain MG1655 grown in minimal medium with glycerol as the carbon source. By using cell lysate from only 3 x 10(8) cells, at least four different tryptic peptides were detected for each of 404 proteins in a short 4-h experiment. At least one peptide with a high reliability score was detected for 986 proteins. Because membrane proteins were under-represented, a second experiment was performed with a preparation enriched in membranes. An additional 161 proteins were detected, of which from half to two-thirds were membrane proteins. Overall, 1,147 different E coli proteins were identified, almost 4 times as many as had been identified previously by using other tools. The protein list was compared with the transcription profile obtained on Affymetrix GeneChips. Expression of 1,113 (97%) of the genes whose protein products were found was detected at the mRNA level. The arithmetic mean mRNA signal intensity for these genes was 3-fold higher than that for all 4,300 protein-coding genes of E coli. Thus, GeneChip data confirmed the high reliability of the protein list, which contains about one-fourth of the proteins of E coli. Detection of even those membrane proteins and proteins of undefined function that are encoded by the same operons (transcriptional units) encoding proteins on the list remained low.
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页码:9232 / 9237
页数:6
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