Ciesielski Grzegorz L, Hytönen Vesa P, Kaguni Laurie S
Institute of Biosciences and Medical Technology, University of Tampere, Tampere, 33014, Finland.
Fimlab Laboratories, Biokatu 4, Tampere, 33101, Finland.
Methods Mol Biol. 2016;1351:223-31. doi: 10.1007/978-1-4939-3040-1_17.
A lack of effective treatment for mitochondrial diseases prompts scientists to investigate the molecular processes that underlie their development. The major cause of mitochondrial diseases is dysfunction of the sole mitochondrial DNA polymerase, DNA polymerase γ (Pol γ). The development of treatment strategies will require a detailed characterization of the molecular properties of Pol γ. A novel technique, biolayer interferometry, allows one to monitor molecular interactions in real time, thus providing an insight into the kinetics of the process. Here, we present an application of the biolayer interferometry technique to characterize the fundamental reactions that Pol γ undergoes during the initiation phase of mitochondrial DNA replication: holoenzyme formation and binding to the primer-template.
线粒体疾病缺乏有效的治疗方法,这促使科学家们去研究其发病背后的分子过程。线粒体疾病的主要原因是唯一的线粒体DNA聚合酶——DNA聚合酶γ(Pol γ)功能障碍。治疗策略的开发需要对Pol γ的分子特性进行详细表征。一种新技术——生物层干涉术,能够实时监测分子间相互作用,从而深入了解该过程的动力学。在此,我们展示了生物层干涉术在表征Pol γ在线粒体DNA复制起始阶段所经历的基本反应中的应用:全酶形成以及与引物模板的结合。