Isolation and incubation conditions to study heart mitochondrial protein synthesis.

Although much is now known with regard to the processes of mammalian mitochondrial gene expression, relatively little is known concerning the quantitative regulation of this pathway in response to hormones or other physiological stimuli. This has been caused, in large part, by the lack of adequate assay systems in which such processes can be meaningfully measured. The purpose of this and the companion paper [E. E. McKee, B. L. Grier, G. S. Thompson, A. C. F. Leung, and J. D. McCourt. Am. J. Physiol. 258 [Endocrinol. Metab. 21):E503-E510, 1990] is to describe a system in which the quantitative regulation of mitochondrial protein synthesis in rat heart can be investigated. In this report the conditions for mitochondrial isolation and labeling are described, and the importance of isolating intact, tightly coupled mitochondria in obtaining high and reliable rates of protein synthesis is demonstrated. The highest levels of protein synthesis are obtained in mitochondria isolated from hearts perfused and homogenized in the presence of subtilisin, conditions in which the fastest rates of state 3 respiration and the highest respiratory control ratios are also observed. Analysis of the free amino acid pools indicates that isolated heart mitochondria have a negligible level of endogenous methionine as well as other amino acids. As a result, the concentration and specific radioactivity of the [35S]methionine pool serving protein synthesis could be easily determined. Optimal translation occurred at 30 degrees C at a pH of 7.0-7.2 and required the addition of methionine (20 microM), the other 19 amino acids (0.1 mM each), K+ (60-90 mM), Cl- (30-90 mM), Mg2+ (0.5-5 mM), and bovine serum albumin (1 mg/ml). As shown in the companion paper, adenine nucleotide (0.5-4.0 mM) and oxidizable substrate (10-20 mM glutamate) are also required for isolated heart mitochondrial protein synthesis. Analysis of labeled mitochondrial translation products demonstrated that bona fide mitochondrial peptides were synthesized.

[1]  R. Yatscoff,et al.  Experimental approaches to the study of the biogenesis of mammalian mitochondrial proteins. , 1986, Biochemistry and cell biology = Biochimie et biologie cellulaire.

[2]  R. Doolittle,et al.  URF6, last unidentified reading frame of human mtDNA, codes for an NADH dehydrogenase subunit. , 1986, Science.

[3]  M. Renis,et al.  Mitochondrial DNA, RNA and protein synthesis in normal and hypothyroid developing rat liver. , 1986, Cell differentiation.

[4]  S. Hutson Branched chain alpha-keto acid oxidative decarboxylation in skeletal muscle mitochondria. Effect of isolation procedure and mitochondrial delta pH. , 1986, The Journal of biological chemistry.

[5]  B. Corkey,et al.  Regulation of free and bound magnesium in rat hepatocytes and isolated mitochondria. , 1986, The Journal of biological chemistry.

[6]  D. Boulet,et al.  The translation system of rat heart muscle mitochondria is stimulated following treatment with L-triiodothyronine. , 1985, Biochemical and biophysical research communications.

[7]  P. Watson,et al.  Wiggers Award lecture. Biochemical correlates of myocardial hypertrophy. , 1985, The Physiologist.

[8]  G. Attardi Animal mitochondrial DNA: an extreme example of genetic economy. , 1985, International review of cytology.

[9]  R. O. Poyton,et al.  Mitochondrial gene expression in saccharomyces cerevisiae. I. Optimal conditions for protein synthesis in isolated mitochondria. , 1984, The Journal of biological chemistry.

[10]  R. O. Poyton,et al.  Mitochondrial gene expression in saccharomyces cerevisiae. II. Fidelity of translation in isolated mitochondria from wild type and respiratory-deficient mutant cells. , 1984, The Journal of biological chemistry.

[11]  N. Mills,et al.  Optimization of in vitro protein synthesis by isolated mouse adrenal mitochondria. , 1984, Analytical biochemistry.

[12]  D. Clayton Transcription of the mammalian mitochondrial genome. , 1984, Annual review of biochemistry.

[13]  G. Attardi,et al.  High-resolution electrophoretic fractionation and partial characterization of the mitochondrial translation products from HeLa cells. , 1982, Biochemistry.

[14]  B. Nelson,et al.  Energy requirements for protein synthesis in isolated rat liver mitochondria. , 1982, Biochemical and biophysical research communications.

[15]  D. S. Beattie,et al.  The effect of diabetes on protein synthesis and the respiratory chain of rat skeletal muscle and kidney mitochondria. , 1982, Archives of biochemistry and biophysics.

[16]  D. A. Clayton,et al.  Sequence and gene organization of mouse mitochondrial DNA , 1981, Cell.

[17]  R. O. Poyton,et al.  Cooperative interaction between mitochondrial and nuclear genomes: cytochrome c oxidase assembly as a model. , 1980, Current topics in cellular regulation.

[18]  D. S. Beattie [2] Yeast versus mammalian mitochondrial protein synthesis , 1979 .

[19]  M. Harri Metabolic and cardiovascular responses to prolonged noradrenaline load and their antagonism by beta blockade in the rat. , 1978, Acta physiologica Scandinavica.

[20]  A. Wollenberger,et al.  Accelerated RNA and protein synthesis in mitochondria isolated from unperfused myocardium. Possible involvement of cyclic AMP. , 1978, Journal of molecular and cellular cardiology.

[21]  H. E. Morgan,et al.  Measurement of the rate of protein synthesis and compartmentation of heart phenylalanine. , 1978, The Journal of biological chemistry.

[22]  C. Hoppel,et al.  Biochemical properties of subsarcolemmal and interfibrillar mitochondria isolated from rat cardiac muscle. , 1977, The Journal of biological chemistry.

[23]  T. Mason,et al.  The Biosynthesis of Mitochondrial Proteins , 1974 .

[24]  A. Hochberg,et al.  Artifacts in protein synthesis by mitochondria in vitro , 1972, FEBS letters.

[25]  A. Wollenberger,et al.  Amino acid incorporation into mitochondria from hypertrophying hearts of rats with aortic constriction , 1970 .

[26]  A. Hamberger,et al.  The effect of acute exercise on amino acid incorporation into mitochondria of rabbit tissues. , 1969, Biochimica et biophysica acta.

[27]  R. Basford,et al.  Bacterial contamination and amino acid incorporation by isolated mitochondria. , 1967, The Journal of biological chemistry.

[28]  A. Kroon Protein synthesis in heart mitochondria. I. Amino acid incorporation into the protein of isolated beefheart mitochondria and fractions derived from them by sonic oscillation. , 1963, Biochimica et biophysica acta.

[29]  M. Simpson,et al.  Incorporation of labeled amino acids into the protein of muscle and liver mitochondria. , 1958, Journal of Biological Chemistry.

[30]  O. H. Lowry,et al.  Protein measurement with the Folin phenol reagent. , 1951, The Journal of biological chemistry.