Rathert Philipp, Cheng Xiaodong, Jeltsch Albert
Jacobs University Bremen, Bremen, Germany.
Biotechniques. 2007 Nov;43(5):602, 604, 606 passim. doi: 10.2144/000112623.
We describe a continuous peptide methylation assay using the Neurospora crassa Dim-5 histone H3 lysine 9 (H3K9) methyltransferase as a model system. The assay uses streptavidin FlashPlates coated with target peptide. Since no washing and pipeting steps were required after the addition of the enzyme/S-adenosyl-L-methionine (AdoMet) mixture to the microplate, a continuous readout of the reaction progress was possible. We show that this assay is highly reproducible (with errors in the order of +/- 3%). The continuous assay is well suited for the simultaneous analysis of up to 384 samples, thus allowing for a rapid screening of methylation rates of different substrates under different conditions or in the presence of inhibitors.
我们描述了一种连续肽甲基化测定法,该方法使用粗糙脉孢菌Dim-5组蛋白H3赖氨酸9(H3K9)甲基转移酶作为模型系统。该测定法使用包被有靶肽的链霉亲和素FlashPlates。由于在向微孔板中加入酶/S-腺苷-L-甲硫氨酸(AdoMet)混合物后无需洗涤和移液步骤,因此可以对反应进程进行连续读数。我们表明该测定法具有高度可重复性(误差在±3%左右)。这种连续测定法非常适合同时分析多达384个样品,从而能够在不同条件下或存在抑制剂的情况下快速筛选不同底物的甲基化率。