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关于在含有[32P]磷酸盐的培养基中孵育的脂肪组织和其他组织制剂中[γ-32P]ATP比活性的研究。

Studies on the specific activity of [gamma-32P]ATP in adipose and other tissue preparations incubated with medium containing [32P]phosphate.

作者信息

Hopkirk T J, Denton R M

出版信息

Biochim Biophys Acta. 1986 Feb 21;885(2):195-205. doi: 10.1016/0167-4889(86)90089-3.

Abstract

The specific activity of the gamma-32P position of ATP was measured in various tissue preparations by two methods. One employed HPLC and the enzymatic conversion of ATP to glucose 6-phosphate and ADP. The other was based on the phosphorylation of histone by catalytic subunit of cAMP-dependent protein kinase (Hawkins, P.T., Michell, R.H. and Kirk, C.J. (1983) Biochem. J. 210, 717-720). The HPLC method also allowed the incorporation of 32P into the (alpha + beta)-positions of ATP to be determined. In rat epididymal fat-pad pieces and fat-cell preparations the specific activity of [gamma-32P]ATP attained a steady-state value after 1-2 h incubation in medium containing 0.2 mM [32P]phosphate. Addition of insulin or the beta-agonist isoprenaline increased this value by 5-10% within 15 min. Under these conditions the steady-state specific activity of [gamma-32P]ATP was 30-40% of the initial specific activity of the medium [32P]phosphate. However, if allowance was made for the change in medium phosphate specific activity during incubations the equilibration of the gamma-phosphate position of ATP with medium phosphate was greater than 80% in both preparations. The change in medium phosphate specific activity was a combination of the expected equilibration of [32P]phosphate with exchangeable intracellular phosphate pools plus the net release of substantial amounts of tissue phosphate. At external phosphate concentrations of less than 0.6 mM the loss of tissue phosphate to the medium was the major factor in the change in medium phosphate specific activity. It is concluded that little advantage is gained in employing external phosphate concentrations of less than 0.6 mM in experiments concerned with the incorporation of phosphate into proteins and other intracellular constituents. Indeed, a low external phosphate concentration may cause depletion of important intracellular phosphorus-containing components.

摘要

通过两种方法测定了各种组织制剂中ATP的γ-32P位的比活性。一种方法采用高效液相色谱法(HPLC)以及将ATP酶促转化为6-磷酸葡萄糖和ADP。另一种方法基于环磷酸腺苷(cAMP)依赖性蛋白激酶催化亚基对组蛋白的磷酸化作用(霍金斯,P.T.,米歇尔,R.H.和柯克,C.J.(1983年)《生物化学杂志》210卷,717 - 720页)。HPLC方法还能测定32P掺入ATP的(α + β)位的情况。在大鼠附睾脂肪垫碎片和脂肪细胞制剂中,在含有0.2 mM [32P]磷酸盐的培养基中孵育1 - 2小时后,[γ-32P]ATP的比活性达到稳态值。添加胰岛素或β-激动剂异丙肾上腺素在15分钟内使该值增加5 - 10%。在这些条件下,[γ-32P]ATP的稳态比活性是培养基[32P]磷酸盐初始比活性的30 - 40%。然而,如果考虑到孵育过程中培养基磷酸盐比活性的变化,在两种制剂中ATP的γ-磷酸位与培养基磷酸盐的平衡均大于80%。培养基磷酸盐比活性的变化是[32P]磷酸盐与可交换细胞内磷酸盐池预期平衡以及大量组织磷酸盐净释放的综合结果。在外部磷酸盐浓度低于0.6 mM时,组织磷酸盐向培养基的流失是培养基磷酸盐比活性变化的主要因素。得出的结论是,在涉及磷酸盐掺入蛋白质和其他细胞内成分的实验中,采用低于0.6 mM的外部磷酸盐浓度几乎没有优势。实际上,低外部磷酸盐浓度可能导致重要的细胞内含磷成分耗竭。

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