Toward a Protein Profile of Escherichia coli: Comparison to Its Transcription Profile
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 108cells, at least four different tryptic peptides were detected for each...
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Published in | Proceedings of the National Academy of Sciences - PNAS Vol. 100; no. 16; pp. 9232 - 9237 |
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Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
National Academy of Sciences
05.08.2003
National Acad Sciences |
Subjects | |
Online Access | Get full text |
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Summary: | 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 108cells, 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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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 ObjectType-Article-1 ObjectType-Feature-2 R.W.C. and O.P. contributed equally to this work. To whom correspondence may be addressed at: Department of Plant and Microbial Biology, University of California, 111 Koshland Hall, Berkeley, CA 94720-3102. E-mail: kustu@nature.berkeley.edu, or Department of Chemistry, University of Virginia, McCormick Road, Charlottesville, VA 22901. E-mail: dfh@virginia.edu. Contributed by Sydney Kustu, May 30, 2003 Abbreviation: MS/MS, tandem MS. |
ISSN: | 0027-8424 1091-6490 |
DOI: | 10.1073/pnas.1533294100 |