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Succinyl-CoA:3-ketoacid coenzyme A transferase (SCOT): development of an antibody to human SCOT and diagnostic use in hereditary SCOT deficiency.

作者信息

Song X Q, Fukao T, Mitchell G A, Kassovska-Bratinova S, Ugarte M, Wanders R J, Hirayama K, Shintaku H, Churchill P, Watanabe H, Orii T, Kondo N

机构信息

Department of Pediatrics, Gifu University School of Medicine, Japan.

出版信息

Biochim Biophys Acta. 1997 Apr 12;1360(2):151-6. doi: 10.1016/s0925-4439(96)00074-9.

Abstract

Succinyl-CoA:3-ketoacid CoA transferase (SCOT) is a key enzyme for ketone body utilization. Hereditary SCOT deficiency in humans (McKusick catalogue number 245050) is characterized by intermittent ketoacidotic attacks and permanent hyperketonemia. Since previously-available antibody to rat SCOT did not crossreact with human SCOT, we developed an antibody against recombinant human SCOT expressed in a bacterial system. The recombinant SCOT was insoluble except under denaturing conditions. Antibody raised to this polypeptide recognized denatured SCOT and proved useful for immunoblot analysis. On immunoblots, SCOT was easily detectable in control fibroblasts and lymphocytes but was detected neither in fibroblast extracts from four SCOT-deficient patients, nor in lymphocytes from two SCOT-deficient patients. These data indicate that immunoblot analysis is useful for diagnosis of SCOT deficiency in combination with enzyme assay.

摘要

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