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2-Mercaptoethanol (BME)

Company: Bio-Rad Laboratories
Catalog#: 1610710
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Expression and Purification of Recombinant Skd3 (Human ClpB) Protein and Tobacco Etch Virus (TEV) Protease from Escherichia coli
Author:
Date:
2020-12-05
[Abstract]  

Skd3 (encoded by human CLPB) is a mitochondrial AAA+ protein comprised of an N-terminal ankyrin-repeat domain and a C-terminal HCLR-clade nucleotide-binding domain. The function of Skd3 has long remained unknown due to challenges in purifying the protein to high quality and near homogeneity. Recently we described Skd3 as a human mitochondrial protein disaggregase that solubilizes proteins in the mitochondrial intermembrane space. This protocol overcomes the challenges associated with purifying Skd3 and allows for in depth in vitro study of Skd3 activity. Tobacco etch virus (TEV) protease is required in the purification of Skd3. Thus, we also describe how to purify high quality TEV protease for use in the purification of Skd3, other purification protocols, and in vitro assays requiring TEV

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[摘要]  [摘要] Skd3(由人类CLPB编码)是一种线粒体AAA +蛋白,由N末端锚蛋白重复域和C末端HCLR分支核苷酸结合域组成。由于在纯化蛋白质达到高质量和接近均质性方面的挑战,Skd3的功能长期未知。最近,我们描述Skd3作为人类线粒体蛋白disaggregase ,在线粒体膜间间隙增溶蛋白。该协议克服了与纯化Skd3相关的挑战,并允许对Skd3活性进行深入的体外研究。Skd3的纯化需要烟草蚀刻病毒(TEV)蛋白酶。因此,我们还描述了如何净化高质量TEV蛋白酶可用于纯化Skd3,其他纯化方案以及需要TEV蛋白酶的体外测定。


[背景] Skd3是一种线粒体AAA +蛋白,与多系统线粒体疾病VII型3-甲基谷氨酸酸尿症(MGCA7)有关(Capo-Chichi等人,2015; Kanabus等人,2015; Saunders等人,, 2015; Wortmann等人,2015 ; Kiykim等人,2016 )。由于在体外研究Skd3的能力有限,因此对生物学功能和这些突变对Skd3活性的影响的研究仍难以捉摸(Cupo和Shorter,2020; ...

Streptavidin Bead Pulldown Assay to Determine Protein Homooligomerization
Author:
Date:
2017-11-20
[Abstract]  Pulldown assay is a conventional method to determine protein-protein interactions in vitro. Expressing a protein of interest with two different tags allows testing whether both versions can be captured via one of the two tags as homooligomeric complex. This protocol is based on streptavidin bead capture of a biotinylated protein and co-associated Flag-tagged protein using Streptavidin MagBeads. [摘要]  Pulldown分析是一种常规的方法来确定蛋白质在体外的相互作用。 用两种不同的标签表达感兴趣的蛋白质可以检测两种标签是否可以通过两种标签之一作为同低聚体复合物来捕获。 该方案基于使用链霉抗生物素蛋白MagBeads的链霉抗生物素蛋白珠捕获生物素化蛋白质和共结合Flag标记蛋白质。
【背景】淀粉样前体蛋白(APP)可以通过其大的胞外结构域及其跨膜结构域形成同型二聚体,在生物学功能中起重要作用。 目前的方案已被用于表征APP跨膜C-末端99个氨基酸片段(C99)的同二聚化(Yan等人,2017)。 该检测的基本原理如图1所示:链霉亲和素包被的MagBeads可以捕获生物素化的蛋白质,这可以拉下相互作用蛋白质,并通过抗FLAG抗体检测。

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图1.基于MagBeads的pull-down测定的原理在该特定的方案中,使用生物素化的Avi-标记的C99蛋白和相关的C99-TEV位点-rTA-Flag蛋白质。

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