Fig 1.
iTRAQ workflow for differential protein profiling in mitochondria from 3-month-old wild type and TazKD mice.
(A) Sample preparation workflow from a preparative SDS-PAGE gel, trypsin digestion, iTRAQ labeling, fractionation by strong cation exchange, followed by nanoLC-MS/MS to produce both protein identification by peptide fragmentation data and relative quantitation from the iTRAQ reporter fragment ions. (B) The preparative SDS-PAGE gel with pre-stained molecular weight markers showing the gel regions collected for trypsin digestion. (C) Overlay of the nano-LC-MS total ion current (TIC) from each of the 20 SCX fractions.
Table 1.
Oligonucleotides used for quantitative PCR analyses.
Fig 2.
(A) Representative 2D-DIGE image of differentially labeled proteins in mitochondria from 3-month-old wild type and TazKD mice.
Proteins with changes in expression levels of at least 1.5-fold are marked with red (decreased) and green (increased) circles. Spot numbers correspond to those in Table 1. (B) Top-rated network of proteins involved in lipid metabolism and associated with altered mitochondrial proteins in TazKD hearts. Shapes denote functional classes of proteins. Shapes in green depict down-regulated proteins; red-colored symbols indicate up-regulated proteins. Proteins in white are theoretically identified by Ingenuity Pathway Knowledge Base analysis. Solid and dashed lines depict direct and indirect interactions, respectively.
Table 2.
Differentially expressed mitochondrial proteins identified by 2D-DIGE and iTRAQ analyses TazKD mice.
Fig 3.
Quantitative analysis of mitochondrial ETC enzymes, myoglobin (MB) and MTHFD2 in cardiac mitochondria of TazKD mice.
(A) Quantification of Taz mRNA levels in hearts of 3 weeks old (P21) and 3 months old (3M) WT and TazKD mice. The expression levels were determined by quantitative RT-PCR and represented as relative normalized expression. (B) Representative Western blots of mitochondrial proteins from TazKD and WT hearts. Mitochondrial proteins (30 μg) were separated by SDS-electrophoresis and subjected to Western blot analysis using a cocktail of monoclonal antibodies specific to individual polypeptides of ETC complexes NDUFA9 (C-I), SDHB (C-II), UQCRC (C-III), COX4 (C-IV) and ATP5A (C-V). Additionally, blots were probed with antibodies specific to Rieske Fe-S cluster protein (UQCRFS1) and myoglobin (MB). Myoglobin content was analyzed in mitochondrial fraction (Mito) and the total cardiac tissue protein extract (T.E.) fractions. Antibodies specific to mitochondrial malate dehydrogenase (MDH) were used as a loading control. The entire (uncropped) images of Western blots are shown in S1 Fig. (C) Quantitative assessments of Western blot analyses. Bars represent fold-changes in band intensities in TazKD samples compared to WT controls. For A and C: Data shown are means ± standard error of mean (SEM). Number of experiments per group is denoted in the corresponding bar. Asterisks indicate significant differences of P≤0.05 (Student’s t-test) between WT and TazKD.
Fig 4.
Evidence of destabilization of mitochondrial supercomplexes in cardiolipin-depleted cardiac mitochondria from TazKD mice.
(A and D) Mitochondria from WT and TazKD hearts were solubilized with digitonin and subjected to blue-native gel electrophoresis (BNGE, first dimension) and then to SDS-gel electrophoresis under denaturing conditions (SDS-PAGE, second dimension). Gels were subjected to western blot analyses with an antibody cocktail specific to subunits of mitochondrial ETC complexes (Anti-OxPhos Cocktail). Bands representing the individual polypeptides that correspond to ETC complexes are marked. In a separate set of experiments, mitochondria from WT (B and C) and TazKD (E and F) hearts were solubilized with lauryl maltoside and subjected to sucrose gradient ultracentrifugation. Individual fractions of the gradient were subjected to western blot analyses using Anti-OxPhos Cocktail (B and E) or FAO enzyme-specific antibodies LCHAD, VLCAD and MCAD (C and F). P—pellet; I—input material (i.e. the solubilized mitochondria preparation that was applied to the sucrose gradient). The scales on the right side depict molecular masses in kilodaltons (kDa).
Fig 5.
Altered Mthfd2 expression in adult TazKD heart.
(A) Quantification of Mthfd2 mRNA levels in hearts of WT and TazKD mice during development. (B) Immunoblots of total protein extracts from 3 month-old WT and TazKD hearts with anti-MTHFD2 antibodies (green). Antibodies specific to mitochondrial malate dehydrogenase (MDH) were used as a loading control (red). (C) Immunofluorescent staining of MTHFD2 in LV sections of 3 month-old WT and TazKD mice revealing localization of MTHFD2 protein (green) in intercalated disks (arrowheads) and myofilaments (MF). Mitochondria were visualized with antibodies specific to complex I subunit NDUFA9 (red). Nuclei were stained with DAPI (blue).
Fig 6.
Structures of mitochondrial respiratory chain complexes that are affected in TazKD mice.
Polypeptides that are quantitatively reduced in TazKD cardiac mitochondria are highlighted with colors. Structurally integrated cardiolipin (CL) molecules within complex III are highlighted in yellow.
Fig 7.
Hypothetical pathophysiological mechanism of Barth syndrome.
In normal mitochondria with high content of CL in the IMM, respiratory complexes are assembled into supercomplexes and form even higher-order structures (hypercomplexes) by interacting with FAO enzymes. In contrast, in CL-depleted mitochondria from BTHS hearts, supercomplexes are destabilized, and the relative quantities of NDUFA5 (C-I), SDHA (C-II), UQCRFS1 and CYC1 (C-III) and ATPA (C-V) are reduced. Defects in respiratory chain complexes would likely induce overproduction of reactive oxygen species (ROS). In CL-deficient mitochondria, disassociation of FAO enzymes from RC complexes would reduce the efficiency of metabolic channeling through these pathways. Reduced oxygen availability at the outer mitochondrial membrane (OMM) due to low myoglobin binding to mitochondria would further diminish aerobic ATP synthesis, but might also reduce generation of ROS.