Abstract
The assembly of cytochrome-c oxidase was studied in human cells cultured in the presence of inhibitors of mitochondrial or cytosolic protein synthesis. Mitochondrial fractions were resolved using twodimensional PAGE (blue native PAGE and tricine/SDS/PAGE) and subsequent western blots were developed with monoclonal antibodies against specific subunits of cytochrome- c oxidase. Proteins were also visualized using metabolic labeling followed by two-dimensional electrophoresis and fluorography. These techniques allowed identification of two assembly intermediates of cytochrome-c oxidase. Assembly of the 13 subunits of cytochrome-c oxidase starts with the association of subunit I with subunit IV. Then a larger subcomplex is formed, lacking only subunits Via and either VIIa or VIIb.
Author supplied keywords
Cite
CITATION STYLE
Nijtmans, L. G. J., Taanman, J. W., Muijsers, A. O., Speijer, D., & Van Den Bogert, C. (1998). Assembly of cytochrome-c oxidase in cultured human cells. European Journal of Biochemistry, 254(2), 389–394. https://doi.org/10.1046/j.1432-1327.1998.2540389.x
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.