Nitration of Tryptophan 372 in Succinyl-CoA:3-Ketoacid CoA Transferase during Aging in Rat Heart Mitochondria

• Published in: Biochemistry (Easton) Vol. 46; no. 35; pp. 10130 - 10144
• Main Authors: Rebrin, Igor, Brégère, Catherine, Kamzalov, Sergey, Gallaher, Timothy K, Sohal, Rajindar S
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 04.09.2007
• Subjects: Acyl Coenzyme A - chemistry; Acyl Coenzyme A - metabolism; Aged; Aging - metabolism; Animals; Coenzyme A-Transferases - chemistry; Coenzyme A-Transferases - metabolism; Humans; Male; Mitochondria - chemistry; Mitochondria - metabolism; Myocardium - chemistry; Myocardium - metabolism; Nitrates - chemistry; Rats; Rats, Inbred F344; Tryptophan - chemistry
• ISSN: 0006-2960; 1520-4995
• DOI: 10.1021/bi7001482

The main objective of this study was to test the hypothesis that in vivo post-translational modifications in proteins, induced by the endogenously generated reactive oxygen and nitrogen molecules, can alter protein function and thereby have an effect on metabolic pathways during the aging process. Succinyl-CoA:3-ketoacid coenzyme A transferase (SCOT), the mitochondrial enzyme involved in the breakdown of ketone bodies in the extrahepatic tissues, was identified in rat heart to undergo age-associated increase in a novel, nitro-hydroxy, addition to tryptophan 372, located in close proximity (∼10 Å) of the enzyme active site. Between 4 and 24 months of age, the molar content of nitration was more than doubled while specific enzyme activity increased significantly. The amount of SCOT protein, however, remained unchanged. In vitro treatment of heart mitochondrial soluble proteins with relatively low concentrations of peroxynitrite enhanced the nitration as well as specific activity of SCOT. Results of this study identify tryptophan to be a specific target of nitration in vivo, for the first time. We hypothesize that increases in tryptophan nitration of SCOT and catalytic activity constitute a plausible mechanism for the age-related metabolic shift toward enhanced ketone body consumption as an alternative source of energy supply in the heart.