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An ultrasensitive enzymatic method for measuring mevalonic acid in serum

机译:测定血清中甲羟戊酸的超灵敏酶法

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摘要

We have developed a simple, precise, and ultrasensitive enzymatic method for measuring serum mevalonic acid (MVA) concentration, which is thought to be a good indicator of the in vivo cholesterol biosynthesis rate. This assay is based on an enzyme cycling reaction and makes use of HMG-CoA reductase (HMGR), thio-NAD, NADH, and CoA. MVA participates in the HMGR cycling reaction, and its level is measured based on the production of thio-NADH, which is determined from the change in absorbance at 405 nm. To achieve high specificity, we used mevalonate kinase (MVK) in addition to HMGR. Only substrates able to participate in both the HMGR cycling reaction and the MVK reaction are measured as MVA. The detection limit for MVA is 0.4 ng/ml (2.7 nmol/l), and the calibration curve for MVA is linear up to 44 ng/ml (300 nmol/l). Regression analysis with 40 serum samples showed the accuracy of quantifying MVA with this enzymatic assay to be comparable to that using LC-MS/MS (correlation: y = 0.83x + 0.24; r = 0.97). This procedure is simple, precise, and robust. It is also rapid and has a high throughput, making it potentially useful for clinical applications.
机译:我们已经开发出一种简单,精确和超灵敏的酶法测定血清甲羟戊酸(MVA)的浓度,该方法被认为是体内胆固醇生物合成速率的良好指标。该测定基于酶循环反应,并利用了HMG-CoA还原酶(HMGR),硫代NAD,NADH和CoA。 MVA参与HMGR循环反应,其水平是根据硫代NADH的产生来测量的,硫代NADH的产生是由405 nm处吸光度的变化确定的。为了实现高特异性,我们除了使用HMGR外还使用了甲羟戊酸激酶(MVK)。仅将能够参与HMGR循环反应和MVK反应的底物测量为MVA。 MVA的检出限为0.4 ng / ml(2.7 nmol / l),MVA的校正曲线为线性,最高可达44 ng / ml(300 nmol / l)。用40个血清样品进行的回归分析表明,用这种酶法测定MVA的准确性与使用LC-MS / MS的准确性相当(相关性:y = 0.83x + 0.24; r = 0.97)。此过程简单,精确且可靠。它也快速并且具有高通量,使其潜在地可用于临床应用。

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