Proteome profile of human urine with two-dimensional liquid phase fractionation
| Autor: | Monica Soldi, Paolo Mocarelli, Cecilia Sarto, Cristina Valsecchi, Fulvio Magni, Vanessa Proserpio, Davide Ticozzi |
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| Přispěvatelé: | Soldi, M, Sarto, C, Valsecchi, C, Magni, F, Proserpio, V, Ticozzi, D, Mocarelli, P |
| Jazyk: | angličtina |
| Rok vydání: | 2005 |
| Předmět: |
Resolution (mass spectrometry)
Proteome Molecular Sequence Data Analytical chemistry Fractionation Urine Mass spectrometry Biochemistry Absorbance Automation Peptide Fragment Humans Electrophoresis Gel Two-Dimensional Trypsin Amino Acid Sequence Molecular Biology Gel electrophoresis Chromatography Chromatofocusing Chemistry Protein Proteins Reproducibility of Results BIO/10 - BIOCHIMICA Peptide Fragments Proteinuria Two-dimensional chromatography Spectrometry Mass Matrix-Assisted Laser Desorption-Ionization Human |
| Popis: | Two-dimensional liquid chromatography separation (2-DL), based on chromatofocusing for first dimension and hydrophobicity for second, can be used as a complementary method to two-dimensional gel electrophoresis (2-DE). A platform now available, ProteomeLab PF 2D provided by Beckman Coulter, (Fullerton, CA, USA), assembles these methods in automation. This system was applied to resolve large numbers of urine proteins. Reproducibility and sensitivity in protein resolution were evaluated in this study using urines collected from male blood donors. About 1000 peaks were detected at a pH range of 4.0-8.5 by applying 1 mg of proteins. Furthermore, the same fractions showing peaks with high absorbance intensities in second dimension were collected and subjected to matrix-assisted laser desorption/ionization-time of flight/mass spectrometry analysis for identification. The results showed that the 2-DL provides high reproducibility of two-dimensional protein map, and lends fractions to subsequent mass spectrometry analysis without the further need for extraction or solubilization of samples as required for spots excised from 2-DE gels. In addition, this system also allows to separate particularly proteins with 40-9 kDa molecular weight. |
| Databáze: | OpenAIRE |
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