School of Biochemistry, University of Bristol, Bristol BS8 1TD, UK. Electronic address: https://twitter.com/hopeneeds.
School of Biochemistry, University of Bristol, Bristol BS8 1TD, UK. Electronic address: https://twitter.com/JamesLorriman.
J Mol Biol. 2023 Jul 1;435(13):168129. doi: 10.1016/j.jmb.2023.168129. Epub 2023 Apr 25.
Mitochondrial protein import is critical for organelle biogenesis, bioenergetic function, and health. The mechanism of which is poorly understood, particularly of the mammalian system. To address this problem we have established an assay to quantitatively monitor mitochondrial import inside mammalian cells. The reporter is based on a split luciferase, whereby the large fragment is segregated in the mitochondrial matrix and the small complementary fragment is fused to the C-terminus of a purified recombinant precursor protein destined for import. Following import the complementary fragments combine to form an active luciferase-providing a sensitive, accurate and continuous measure of protein import. This advance allows detailed mechanistic examination of the transport process in live cells, including the analysis of import breakdown associated with disease, and high-throughput drug screening. Furthermore, the set-up has the potential to be adapted for the analysis of alternative protein transport systems within different cell types, and multicellular model organisms.
线粒体蛋白的输入对于细胞器的生物发生、生物能量功能和健康至关重要。然而,这一机制在很大程度上仍未被理解,特别是在哺乳动物系统中。为了解决这个问题,我们建立了一种定量监测哺乳动物细胞内线粒体输入的测定方法。该报告基于一种分裂的荧光素酶,其中大片段在线粒体基质中分离,而小的互补片段融合到纯化的重组前体蛋白的 C 末端,该蛋白注定要进行输入。输入后,互补片段结合形成活性荧光素酶,提供了一种敏感、准确和连续的蛋白输入测量方法。这一进展使得可以在活细胞中对运输过程进行详细的机制研究,包括分析与疾病相关的输入中断,并进行高通量药物筛选。此外,该设置有可能适用于不同细胞类型和多细胞模式生物中替代蛋白运输系统的分析。