4.8 Article

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

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NATL ACAD SCIENCES
DOI: 10.1073/pnas.1533294100

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  1. NIGMS NIH HHS [R37 GM038361, R01 GM038361, R01 GM037537, GM37537, GM38361] Funding Source: Medline

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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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