Molecular & Cellular Proteomics · 2004 · 133 citations · 47 references
Life SciencesBiochemistryMolecular BiologyMembrane BiochemistryProtein BiochemistryProteomicsMass Spectrometry-based ProteomicsMembrane ProteinsMembrane ProteomicsProtein IdentificationProtein PurificationProtein SeparationChloroplast ProteomicsMembrane Protein AnalysisMembrane Protein IdentificationMembrane Protein PurificationOuter Membrane ProteinsPorin ProteinsSignal PeptidesTwo-dimensional Gel Electrophoresis
In this report, we describe a newly developed method for isolating outer membranes from Synechocystis sp. PCC 6803 cells. The purity of the outer membrane fraction was verified by immunoblot analysis using antibodies against membrane-specific marker proteins. We investigated the protein composition of the outer membrane using two-dimensional gel electrophoresis and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry followed by database identification. Forty-nine proteins were identified corresponding to 29 different gene products. All of the identified proteins have a putative N-terminal signal peptide. About 40% of the proteins identified represent hypothetical proteins with unknown function. Among the proteins identified are a Toc75 homologue, a protein that was initially found in the outer envelope of chloroplasts in pea, as well as TolC, putative porins, and a pilus protein. Other proteins identified include ABC transporters and GumB, which has a suggested function in carbohydrate export. A number of proteases such as HtrA were also found in the outer membrane of Synechocystis sp. PCC 6803.
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Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4
Ulrich K. Laemmli · Nature · 1970 · 251.6K citations
Takakazu Kaneko, Shusei Sato, Haruru Kotani et al. · DNA Research · 1996 · 2.4K citations · Full text