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SHR Neuro Krebs Kardio Lipid Stoffw Microb

Becker, JC; Houben, R; Vetter, CS; Brocker, EB.
2-D differential membrane proteome analysis of scarce protein samples.
Proteomics. 2006; 6(16):4506-4513 Doi: 10.1002/pmic.200600169 [OPEN ACCESS]
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Führende Autor*innen der Med Uni Graz
Becker Jürgen Christian
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Abstract:
Proteome studies with small sample amounts are difficult to perform, especially when membrane proteins are the focus of interest. In our study a new method for the analysis of scarce membrane protein samples combining large gel 2-D-CTAB/SDS-PAGE with fluorescence dye saturation labelling (satDIGE) was developed, allowing a highly sensitive differential analysis of different cell states. After Triton X-114 phase partitioning, enriched membrane protein samples of T cells were labelled at cysteine residues using fluorescence dyes and separated by large gel 2D-CTAB/SDS-PAGE. For a differential analysis 3 mug protein was found to be sufficient to detect proteins in a widespread well-separated diagonal spot pattern.
Find related publications in this database (using NLM MeSH Indexing)
Amino Acid Sequence -
Animals -
Cells, Cultured -
Electrophoresis, Gel, Two-Dimensional -
Fluorescent Dyes - chemistry
Humans -
Membrane Proteins - analysis Membrane Proteins - isolation and purification
Mice -
Molecular Sequence Data -
Proteome -
Spectrometry, Mass, Electrospray Ionization -

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