Abstract
Escherichia coli is a gram-negative bacterium that causes sepsis and infections of the nervous system, and the digestive and urinary tracts. The availability of the complete nucleotide sequence encoding the E. coli K-12 genome has made this organism an excellent model for proteomic studies. Semi-preparative two-dimensional electrophoresis, including liquid phase isoelectric focusing (IEF), one-dimensional sodium dodecyl sulfate (SDS) polyacrylamide gel electrophoresis (PAGE) and gel elution, have for the first time been used in combination with matrix-assisted laser desorption/ionisation time-of-flight mass spectrometry (MALDI-TOFMS), electrospray tandem mass spectrometry and database searching for rapid separation of proteins from a uropathogenic strain of E. coli. The identity of 30 proteins, including the membrane protein nmpC, was obtained using this approach.
| Original language | English |
|---|---|
| Pages (from-to) | 428-32 |
| Journal | Rapid Communications in Mass Spectrometry |
| Volume | 15 |
| Issue number | 6 |
| DOIs | |
| Publication status | Published - 2001 |
| Externally published | Yes |
Free keywords
- Bacterial Proteins
- Cell Fractionation
- Electrophoresis, Gel, Two-Dimensional
- Escherichia coli
- Isoelectric Focusing
- Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
- Journal Article
- Research Support, Non-U.S. Gov't
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