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dc.contributor.authorAcestor, Nathalie
dc.contributor.authorZíková, Alena
dc.contributor.authorDalley, Rachel A.
dc.contributor.authorAnupama, Atashi
dc.contributor.authorPanigrahi, Aswini Kumar
dc.contributor.authorStuart, Kenneth D.
dc.date.accessioned2015-08-03T09:04:28Z
dc.date.available2015-08-03T09:04:28Z
dc.date.issued2011-05-24
dc.identifier.issn15359476
dc.identifier.pmid21610103
dc.identifier.doi10.1074/mcp.M110.006908
dc.identifier.urihttp://hdl.handle.net/10754/561781
dc.description.abstractThe mitochondrial respiratory chain is comprised of four different protein complexes (I-IV), which are responsible for electron transport and generation of proton gradient in the mitochondrial intermembrane space. This proton gradient is then used by F oF 1-ATP synthase (complex V) to produce ATP by oxidative phosphorylation. In this study, the respiratory complexes I, II, and III were affinity purified from Trypanosoma brucei procyclic form cells and their composition was determined by mass spectrometry. The results along with those that we previously reported for complexes IV and V showed that the respiratome of Trypanosoma is divergent because many of its proteins are unique to this group of organisms. The studies also identified two mitochondrial subunit proteins of respiratory complex IV that are encoded by edited RNAs. Proteomics data from analyses of complexes purified using numerous tagged component proteins in each of the five complexes were used to generate the first predicted protein-protein interaction network of the Trypanosoma brucei respiratory chain. These results provide the first comprehensive insight into the unique composition of the respiratory complexes in Trypanosoma brucei, an early diverged eukaryotic pathogen. © 2011 by The American Society for Biochemistry and Molecular Biology, Inc.
dc.description.sponsorshipThis work was supported by National Institutes of Health grant AI065935 to KS. AZ received support from grant 204/09/P563 from the Grant Agency of the Czech Republic. Research was conducted using equipment made possible by support from the Economic Development Administration - US Department of Commerce and the M.J. Murdock Charitable Trust.
dc.publisherAmerican Society for Biochemistry & Molecular Biology (ASBMB)
dc.relation.urlhttp://www.ncbi.nlm.nih.gov/pmc/articles/PMC3186196
dc.titleTrypanosoma brucei mitochondrial respiratome: Composition and organization in procyclic form
dc.typeArticle
dc.contributor.departmentBioscience Core Lab
dc.contributor.departmentCore Labs
dc.identifier.journalMolecular & Cellular Proteomics
dc.identifier.pmcidPMC3186196
dc.contributor.institutionSeattle Biomedical Research Institute, 307 Westlake Ave N, Seattle, WA 98109-5219, United States
dc.contributor.institutionBiology Center, Institute of Parasitology, University of South Bohemia, České Budějovice, Czech Republic
kaust.personPanigrahi, Aswini Kumar
dc.date.published-online2011-05-24
dc.date.published-print2011-09


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