Solubilization of Proteins in 2DE: An Outline
Protein solubilization for two-dimensional electrophoresis (2DE) has to break molecular interactions to separate the biological contents of the material of interest into isolated and intact polypeptides. This must be carried out in conditions compatible with the first dimension of 2DE, namely isoelectric focusing. In addition, the extraction process must enable easy removal of any nonprotein component interfering with the isoelectric focusing. The constraints brought in this process by the peculiar features of isoelectric focusing are discussed, as well as their consequences in terms of possible solutions and limits for the solubilization process.
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Recording of Ion Channel Activity in Planar Lipid Bilayer Experiments
Planar lipid bilayer is an electrophysiological technique th...
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Application of Microscope-Based FRET to Study Molecular Interactions in Focal Adhesions of Live Cell
This chapter describes the use of microscope-based fluoresce...