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利用冷冻电镜技术对 Twinkle 线粒体 DNA 解旋酶进行结构分析的方法。

Method for the structural analysis of Twinkle mitochondrial DNA helicase by cryo-EM.

机构信息

Mitochondrial DNA Replication Group, Genome Integrity and Structural Biology Laboratory, National Institute of Environmental Health Sciences, NIH, Research Triangle Park, NC 27709, USA.

Molecular Microscopy Consortium, Genome Integrity and Structural Biology Laboratory, National Institute of Environmental Health Sciences, NIH, Research Triangle Park, NC 27709, USA.

出版信息

Methods. 2022 Sep;205:263-270. doi: 10.1016/j.ymeth.2022.06.012. Epub 2022 Jun 30.

Abstract

The mitochondrial replisome replicates the 16.6 kb mitochondria DNA (mtDNA). The proper functioning of this multicomponent protein complex is vital for the integrity of the mitochondrial genome. One of the critical protein components of the mitochondrial replisome is the Twinkle helicase, a member of the Superfamily 4 (SF4) helicases. Decades of research has uncovered common themes among SF4 helicases including self-assembly, ATP-dependent translocation, and formation of protein-protein complexes. Some of the molecular details of these processes are still unknown for the mitochondria SF4 helicase, Twinkle. Here, we describe a protocol for expression, purification, and single-particle cryo-electron microscopy of the Twinkle helicase clinical variant, W315L, which resulted in the first high-resolution structure of Twinkle helicase. The methods described here serve as an adaptable protocol to support future high-resolution studies of Twinkle helicase or other SF4 helicases.

摘要

线粒体复制体复制 16.6kb 的线粒体 DNA(mtDNA)。这个多成分蛋白复合物的正常功能对于线粒体基因组的完整性至关重要。线粒体复制体的关键蛋白成分之一是 Twinkle 解旋酶,它是 Superfamily 4(SF4)解旋酶家族的成员。数十年的研究揭示了 SF4 解旋酶之间的一些共同主题,包括自组装、ATP 依赖性易位和蛋白质-蛋白质复合物的形成。对于线粒体 SF4 解旋酶 Twinkle,这些过程的一些分子细节仍然未知。在这里,我们描述了一种表达、纯化和单颗粒冷冻电子显微镜技术的方案,用于 W315L 临床变异型 Twinkle 解旋酶,这是首次获得 Twinkle 解旋酶的高分辨率结构。这里描述的方法可以作为一个适应性的方案,以支持未来对 Twinkle 解旋酶或其他 SF4 解旋酶的高分辨率研究。

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