Key result
LC-MS/MS analysis of Trypanosoma brucei mitochondrial membranes reveals ~50% of transmembrane proteins lack known function.
Why the study?
The protein composition of Trypanosoma brucei mitochondrial membranes was not comprehensively characterized to understand their specific functions and structures.
The study provides a comprehensive profile of the composition and sub-organellar location of proteins in the T. brucei mitochondrion.
May inform antiparasitic target discovery; leaves open functional roles of ~100 uncharacterized proteins.
Mitochondria consist of four compartments, outer membrane, intermembrane space, inner membrane, and matrix; each harboring specific functions and structures. In this study, we used LC-MS/MS to characterize the protein composition of Trypanosoma brucei mitochondrial (mt) membranes, which were enriched by different biochemical fractionation techniques. The analyses identified 202 proteins that contain one or more transmembrane domain(s) and/or positive GRAVY scores. Of these, various criteria were used to assign 72 proteins to mt membranes with high confidence, and 106 with moderate-to-low confidence. The sub-cellular localization of a selected subset of 13 membrane assigned proteins was confirmed by tagging and immunofluorescence analysis. While most proteins assigned to mt membrane have putative roles in metabolic, energy generating, and transport processes, approximately 50% have no known function. These studies result in a comprehensive profile of the composition and sub-organellar location of proteins in the T. brucei mitochondrion thus, providing useful information on mt functions.
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Acestor et al. (2009) studied Trypanosoma brucei. LC-MS/MS biochemical fractionation was evaluated on Protein composition of mitochondrial membranes. LC-MS/MS analysis of Trypanosoma brucei mitochondrial membranes identified 202 proteins with transmembrane domains, of which approximately 50% have no known function.
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