Department of Biochemistry, University of Utah, Salt Lake City, UT 84112, USA.
Methods. 2017 Aug 15;126:54-65. doi: 10.1016/j.ymeth.2017.07.012. Epub 2017 Jul 16.
The Dicer family of ribonucleases plays a key role in small RNA-based regulatory pathways by generating short dsRNA fragments that modulate expression of endogenous genes, or protect the host from invasive nucleic acids. Beginning with its initial discovery, biochemical characterization of Dicer has provided insight about its catalytic properties. However, a comprehensive understanding of how Dicer's domains contribute to substrate-specific recognition and catalysis is lacking. One reason for this void is the lack of high-resolution structural information for a metazoan Dicer in the apo- or substrate-bound state. Both biochemical and structural studies are facilitated by large amounts of highly purified, active protein, and Dicer enzymes have historically been recalcitrant to overexpression and purification. Here we describe optimized procedures for the large-scale expression of Dicer in baculovirus-infected insect cells. We then outline a three-step protocol for the purification of large amounts (3-4mg of Dicer per liter of insect cell culture) of highly purified and active Dicer protein, suitable for biochemical and structural studies. Our methods are general and are extended to enable overexpression, purification and biochemical characterization of accessory dsRNA binding proteins that interact with Dicer and modulate its catalytic activity.
核糖核酸酶家族的 Dicer 在基于小 RNA 的调控途径中发挥着关键作用,通过生成短双链 RNA 片段来调节内源性基因的表达,或保护宿主免受入侵核酸的侵害。从最初的发现开始,Dicer 的生化特性研究就为其催化特性提供了深入的了解。然而,对于 Dicer 的结构域如何有助于底物特异性识别和催化,我们仍然缺乏全面的理解。造成这种空白的一个原因是缺乏原核生物或底物结合状态下的后生动物 Dicer 的高分辨率结构信息。大量高度纯化、活性的蛋白质有助于生化和结构研究,而 Dicer 酶在历史上一直难以过表达和纯化。在这里,我们描述了在杆状病毒感染的昆虫细胞中大规模表达 Dicer 的优化程序。然后,我们概述了一个三步法方案,用于从昆虫细胞培养物中纯化大量(每升 3-4 毫克)高度纯化和活性的 Dicer 蛋白,该方法适用于生化和结构研究。我们的方法具有通用性,并扩展到能够过表达、纯化和生化表征与 Dicer 相互作用并调节其催化活性的辅助双链 RNA 结合蛋白。