Uhler Jay P, Alexandersson Ulrika, Falkenberg Maria
Department of Medical Biochemistry and Cell Biology, University of Gothenburg, Gothenburg, Sweden.
Methods Mol Biol. 2023;2615:191-201. doi: 10.1007/978-1-0716-2922-2_14.
TWINKLE is an essential helicase that unwinds the duplex mitochondrial genome during DNA replication. In vitro assays using purified recombinant forms of the protein have been an instrumental tool for gaining mechanistic insights about TWINKLE and its function at the replication fork. Here we present methods to probe the helicase and ATPase activities of TWINKLE. For the helicase assay, TWINKLE is incubated with a radiolabeled oligonucleotide annealed to an M13mp18 single-stranded DNA template. TWINKLE will displace the oligonucleotide, which is then visualized by gel electrophoresis and autoradiography. To measure the ATPase activity of TWINKLE, a colorimetric assay is used, which quantifies the release of phosphate upon ATP hydrolysis by TWINKLE.
TWINKLE是一种重要的解旋酶,在DNA复制过程中解开双链线粒体基因组。使用纯化的重组形式蛋白质进行的体外测定,一直是深入了解TWINKLE及其在复制叉处功能机制的重要工具。在此,我们介绍检测TWINKLE解旋酶和ATP酶活性的方法。对于解旋酶测定,将TWINKLE与退火到M13mp18单链DNA模板上的放射性标记寡核苷酸一起孵育。TWINKLE会置换寡核苷酸,然后通过凝胶电泳和放射自显影进行可视化。为了测量TWINKLE的ATP酶活性,使用比色测定法,该方法可量化TWINKLE水解ATP时释放的磷酸盐量。