School of Chemistry, University of Edinburgh, The King's Buildings, Edinburgh, EH9 3JJ, UK.
Biochem Biophys Res Commun. 2010 Jul 23;398(2):254-9. doi: 10.1016/j.bbrc.2010.06.069. Epub 2010 Jun 19.
We describe the fusion of enhanced green fluorescent protein to the C-terminus of the HsdS DNA sequence-specificity subunit of the Type I DNA modification methyltransferase M.EcoKI. The fusion expresses well in vivo and assembles with the two HsdM modification subunits. The fusion protein functions as a sequence-specific DNA methyltransferase protecting DNA against digestion by the EcoKI restriction endonuclease. The purified enzyme shows Förster resonance energy transfer to fluorescently-labelled DNA duplexes containing the target sequence and to fluorescently-labelled ocr protein, a DNA mimic that binds to the M.EcoKI enzyme. Distances determined from the energy transfer experiments corroborate the structural model of M.EcoKI.
我们描述了将增强型绿色荧光蛋白融合到 I 型 DNA 修饰甲基转移酶 M.EcoKI 的 HsdS DNA 序列特异性亚基的 C 末端。融合蛋白在体内表达良好,并与两个 HsdM 修饰亚基组装。融合蛋白作为一种序列特异性 DNA 甲基转移酶,可保护 DNA 免受 EcoKI 限制内切酶的消化。纯化的酶与含有靶序列的荧光标记 DNA 双链体和荧光标记的 ocr 蛋白(一种与 M.EcoKI 酶结合的 DNA 模拟物)发生Förster 共振能量转移。从能量转移实验中确定的距离证实了 M.EcoKI 的结构模型。