Seglen P O, Solheim A E
Biochim Biophys Acta. 1978 Oct 24;520(3):630-41. doi: 10.1016/0005-2787(78)90148-x.
Protein synthesis in isolated rat hepatocytes has been measured by the incorporation of [14C]valine at high concentration and constant specific activity (5 mmol/l and 315 muCi/l). Protein synthesis was stimulated by the addition of an amino acid mixture, and by a number of individual amino acids alone, most notably alanine. Energy substrates (lactate, pyruvate) stimulated protein synthesis to the same extent as alanine, suggesting that a major part of the amino acid effect could be due to the provision of energy. Aminooxyacetate, an inhibitor of glutamate transaminases, inhibited protein synthesis strongly (70%), and abolished the stimulatory effects of alanine and energy substrates. This could indicate that hepatocytic protein synthesis is subject to positive control by a transamination-dependent agent.
通过在高浓度和恒定比活度(5 mmol/L和315 μCi/L)下掺入[14C]缬氨酸来测定分离的大鼠肝细胞中的蛋白质合成。添加氨基酸混合物以及单独的多种个别氨基酸(最显著的是丙氨酸)可刺激蛋白质合成。能量底物(乳酸、丙酮酸)刺激蛋白质合成的程度与丙氨酸相同,这表明氨基酸效应的主要部分可能归因于能量的提供。谷氨酸转氨酶抑制剂氨基氧乙酸强烈抑制蛋白质合成(70%),并消除丙氨酸和能量底物的刺激作用。这可能表明肝细胞蛋白质合成受转氨依赖性因子的正向调控。