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人肝脏中的磷酸烯醇式丙酮酸羧激酶活性

Phosphoenolpyruvate carboxykinase activity in human liver.

作者信息

McGraw C A, Vawter G F, Hug G

出版信息

Forensic Sci Int. 1986 Feb-Mar;30(2-3):143-54. doi: 10.1016/0379-0738(86)90009-5.

Abstract

The activity of phosphoenolpyruvate carboxykinase (EC 4.1.1.32) (PEPCK), a rate-limiting gluconeogenic enzyme, was found decreased by others in genetically determined disorders and in Sudden Infant Death Syndrome (SIDS). To understand these findings, we made a systematic study of normal human hepatic PEPCK activities in specimens obtained under various conditions from patients not suspected of having SIDS. PEPCK was assayed by the method of Ballard and Hanson [J. Biol. Chem., 244 (1969) 5625] and activity reported as units (1 mumol/min) per gram protein. Intra-assay precision was 4.1% (n = 1094); inter-assay precision using the same homogenate was 10.4% (n = 51); and inter-assay precision using different homogenates of the same tissue specimen was 16.3% (n = 17). The assay was linear with time and enzyme concentration for at least 60 min up to 1.3 mU/assay and for at least 5 min up to 20 mU/assay. Biopsy specimens had significantly (P = 0.015) higher PEPCK activity, 12.60 +/- 3.01 U/g (range 3.5-10.4, n = 9) compared to specimens obtained at autopsy, 3.20 +/- 0.45 U/g (range 0-8.6, n = 33). Specific activity was not significantly correlated with the patient's age, fresh vs. frozen tissue, postmortem intervals up to 68 h, or length of storage at -70 degrees C up to 21 years. One patient had activity at autopsy (tissue obtained less than 2 h postmortem) 26% less than was observed in his biopsy specimen. Autopsy samples separated by differential centrifugation into mitochondrial and cytosolic fractions and checked with marker enzymes ornithine transcarbamylase (mitochondrial) and arginase (cytosolic) had considerable cross-contamination between the two fractions in fresh and frozen specimens.

摘要

磷酸烯醇式丙酮酸羧激酶(EC 4.1.1.32)(PEPCK)是糖异生途径中的限速酶,在遗传性疾病和婴儿猝死综合征(SIDS)中,其他人发现其活性降低。为了理解这些发现,我们对从无SIDS嫌疑患者在各种条件下获取的标本中的正常人类肝脏PEPCK活性进行了系统研究。PEPCK采用Ballard和Hanson的方法进行测定[《生物化学杂志》,244 (1969) 5625],活性以每克蛋白质的单位数(1微摩尔/分钟)报告。批内精密度为4.1%(n = 1094);使用相同匀浆的批间精密度为10.4%(n = 51);使用同一组织标本的不同匀浆的批间精密度为16.3%(n = 17)。该测定在长达1.3 mU/测定时至少60分钟内以及在长达20 mU/测定时至少5分钟内与时间和酶浓度呈线性关系。活检标本的PEPCK活性显著更高(P = 0.015),为12.60±3.01 U/g(范围3.5 - 10.4,n = 9),而尸检获得的标本为3.20±0.45 U/g(范围0 - 8.6,n = 33)。比活性与患者年龄、新鲜组织与冷冻组织、长达68小时的死后间隔或在-70℃下长达21年的储存时间均无显著相关性。一名患者尸检时(死后不到2小时获取的组织)的活性比其活检标本中观察到的活性低26%。通过差速离心将尸检样本分离成线粒体和胞质部分,并用鸟氨酸转氨甲酰酶(线粒体)和精氨酸酶(胞质)这两种标记酶进行检查,结果显示新鲜和冷冻标本中这两部分之间存在相当程度的交叉污染。

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