首页> 美国卫生研究院文献>Nucleic Acids Research >Determination of methylation specificity of sequence-specific DNA methyltransferases using matrix assisted laser desorption/ionization time-of-flight mass spectrometry.
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Determination of methylation specificity of sequence-specific DNA methyltransferases using matrix assisted laser desorption/ionization time-of-flight mass spectrometry.

机译:使用基质辅助激光解吸/电离飞行时间质谱测定序列特异性DNA甲基转移酶的甲基化特异性。

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摘要

We describe here a sensitive and straightforward method for characterizing the methylation specificity of type II DNA methyltransferase (MTase) using matrix-assisted laser desorption/ionization time-of-flight (MALDI-TOF) mass spectrometry. DNA substrate, prepared by ligation of a commercially available oligonucleotide, was modified by the subject MTase, and was derivatized to a mixture of single-stranded oligonucleotides through endonuclease treatment, heat-denaturation and limited digestion by 3'-terminus-specific phosphodiesterase I. MALDI-TOF mass spectrometry was used to determine the mass differences between the digestion products, and the methylated nucleotide was explicitly identified by the mass increase of 14 Da due to the base modification. The method was applicable to the three representative MTases M. Eco RI, M. Bam HI and M. Hae III.
机译:我们在这里描述了一种灵敏而简单的方法,用于使用基质辅助激光解吸/电离飞行时间(MALDI-TOF)质谱法表征II型DNA甲基转移酶(MTase)的甲基化特异性。通过连接市售的寡核苷酸制备的DNA底物经过主题MTase修饰,并通过内切核酸酶处理,热变性和3'-末端特异性磷酸二酯酶I的有限消化衍生化为单链寡核苷酸的混合物。 MALDI-TOF质谱用于确定消化产物之间的质量差异,通过碱基修饰使质量增加14 Da,从而明确鉴定出甲基化核苷酸。该方法适用于三个代表性的MTases M. Eco RI,M。Bam HI和M. Hae III。

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