Newman Laura E, Schiavon Cara, Kahn Richard A
Department of Biochemistry, Emory University School of Medicine , Atlanta, GA, USA.
Cell Logist. 2016 Oct 13;6(4):e1247939. doi: 10.1080/21592799.2016.1247939. eCollection 2016.
We describe the construction and uses of a series of plasmids for directing expression to varied levels of exogenous proteins targeted to the mitochondrial matrix or intermembrane space. We found that the level of protein expression achieved, the kinetics of expression and mitochondrial import, and half-life after import can each vary with the protein examined. These factors should be considered when directing localization of an exogenous protein to mitochondria for rescue, proteomics, or other approaches. We describe the construction of a collection of plasmids for varied expression of proteins targeted to the mitochondrial matrix or intermembrane space, using previously defined targeting sequences and strength CMV promoters. The limited size of these compartments makes them particularly vulnerable to artifacts from over-expression. We found that different proteins display different kinetics of expression and import that should be considered when analyzing results from this approach. Finally, this collection of plasmids has been deposited in the Addgene plasmid repository to facilitate the ready access and use of these tools.
我们描述了一系列质粒的构建和用途,这些质粒用于将外源蛋白定向表达至线粒体基质或膜间隙的不同水平。我们发现,所实现的蛋白表达水平、表达和线粒体导入的动力学以及导入后的半衰期,均会因所检测的蛋白而异。当将外源蛋白定位于线粒体以进行拯救、蛋白质组学或其他方法时,应考虑这些因素。我们描述了一系列质粒的构建,这些质粒利用先前定义的靶向序列和不同强度的巨细胞病毒(CMV)启动子,实现靶向线粒体基质或膜间隙的蛋白的不同表达。这些区室的有限大小使其特别容易受到过表达产生的假象的影响。我们发现,不同的蛋白表现出不同的表达和导入动力学,在分析此方法的结果时应予以考虑。最后,这一系列质粒已保藏于Addgene质粒库,以方便这些工具的便捷获取和使用。