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磷脂酰乙醇胺甲基化研究中的陷阱与问题。

Pitfalls and problems in studies on the methylation of phosphatidylethanolamine.

作者信息

Audubert F, Vance D E

出版信息

J Biol Chem. 1983 Sep 10;258(17):10695-701.

PMID:6885797
Abstract

Recent articles have confused the steady state concentration of radioactivity in N-methylphosphatidylethanolamine (PME) and N,N-dimethylphosphatidylethanolamine (PDE) with the amount of these products formed during the conversion of phosphatidylethanolamine (PE) to phosphatidylcholine (PC). This paper clarifies this problem and reports the apparent Km values for AdoMet and pH optima for the conversion of PE to PME, PDE, and PC by rat liver microsomes. We purified AdoMet and [methyl-3H]AdoMet and measured the transfer of tritium to PME, PDE, and PC as a function of time. There was an initial lag in the formation of [3H]PC followed by linear incorporation of isotope. In contrast, labeled PME and PDE reached and maintained steady state levels within 1 to 2 min. Hence, calculations of the rate of formation of PME, PDE, and PC must take into account the subsequent conversion of PME and PDE to PC. The PE N-methyltransferase was assayed at pH 6.6, 9.2, and 10.25 and the apparent Km for AdoMet for the three methylation reactions was calculated. The formation of PME was best estimated by the dpm in PME + 1/2 dpm in PDE + 1/3 dpm in PC. The synthesis of PDE from PME was estimated from 1/2 dpm in PDE and 1/3 dpm in PC, and the formation of PC from PDE estimated by 1/3 dpm in PC. The apparent Km for AdoMet at pH 10.25 for the conversion of PE to PME was 58 microM, PME to PDE was 65 microM, and PDE to PC was 96 microM. The pH optimum for each of these methylation reactions was 10.25. This high value was not due to alkaline degradation of AdoMet or denaturation of the enzyme. The apparent Km for AdoMet was also estimated for the conversion of exogenous PME to PDE (50 microM) and exogenous PDE to PC (45 microM). Since recent studies on the methylation of PE have not taken into account the conversion of newly formed PME and PDE to PC, the results and conclusions about apparent Km values for AdoMet, pH optima, and the number of enzymes involved must be re-evaluated.

摘要

近期的文章将N-甲基磷脂酰乙醇胺(PME)和N,N-二甲基磷脂酰乙醇胺(PDE)中放射性的稳态浓度与磷脂酰乙醇胺(PE)转化为磷脂酰胆碱(PC)过程中形成的这些产物的量混淆了。本文澄清了这个问题,并报道了大鼠肝微粒体将PE转化为PME、PDE和PC时,腺苷甲硫氨酸(AdoMet)的表观Km值和pH最适值。我们纯化了AdoMet和[甲基-3H]AdoMet,并测量了氚向PME、PDE和PC的转移随时间的变化。[3H]PC的形成最初有一个延迟期,随后同位素呈线性掺入。相比之下,标记的PME和PDE在1至2分钟内达到并维持稳态水平。因此,计算PME、PDE和PC的形成速率时必须考虑PME和PDE随后向PC的转化。在pH 6.6、9.2和10.25下测定了PE N-甲基转移酶,并计算了三个甲基化反应中AdoMet的表观Km值。PME的形成最好通过PME中的每分钟衰变数(dpm)+ 1/2 PDE中的dpm + 1/3 PC中的dpm来估计。由PME合成PDE可根据PDE中的1/2 dpm和PC中的1/3 dpm来估计,由PDE合成PC可根据PC中的1/3 dpm来估计。在pH 10.25下,PE转化为PME时AdoMet的表观Km值为58 microM,PME转化为PDE时为65 microM,PDE转化为PC时为96 microM。这些甲基化反应各自的pH最适值为10.25。这个高值并非由于AdoMet的碱性降解或酶的变性。还估计了外源性PME转化为PDE(50 microM)和外源性PDE转化为PC(45 microM)时AdoMet的表观Km值。由于近期关于PE甲基化的研究没有考虑新形成的PME和PDE向PC的转化,因此关于AdoMet的表观Km值、pH最适值以及所涉及酶的数量的结果和结论必须重新评估。

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