1 Lead Discovery Center GmbH, Dortmund, Germany.
2 Institute of Biomedicine, University of Gothenburg, Goteborg, Sweden.
SLAS Discov. 2017 Apr;22(4):378-386. doi: 10.1177/2472555217690326. Epub 2017 Jan 31.
Mitochondria harbor the oxidative phosphorylation (OXPHOS) system, which under aerobic conditions produces the bulk of cellular adenosine triphosphate (ATP). The mitochondrial genome encodes key components of the OXPHOS system, and it is transcribed by the mitochondrial RNA polymerase, POLRMT. The levels of mitochondrial transcription correlate with the respiratory activity of the cell. Therefore, compounds that can increase or decrease mitochondrial gene transcription may be useful for fine-tuning metabolism and could be used to treat metabolic diseases or certain forms of cancer. We here report the establishment of a novel high-throughput assay technology that has allowed us to screen a library of 430,000 diverse compounds for effects on mitochondrial transcription in vitro. Following secondary screens facilitated by the same assay principle, we identified 55 compounds that efficiently and selectively inhibit mitochondrial transcription and that are active also in cell culture. Our method is easily adaptable to other RNA or DNA polymerases and varying spectroscopic detection technologies.
线粒体拥有氧化磷酸化(OXPHOS)系统,该系统在有氧条件下生成细胞三磷酸腺苷(ATP)的大部分。线粒体基因组编码 OXPHOS 系统的关键组成部分,由线粒体 RNA 聚合酶 POLRMT 转录。线粒体转录的水平与细胞的呼吸活性相关。因此,能够增加或减少线粒体基因转录的化合物可能有助于精细调节代谢,可用于治疗代谢疾病或某些形式的癌症。我们在此报告建立了一种新型高通量检测技术,使我们能够筛选 430,000 种不同化合物对体外线粒体转录的影响。通过相同检测原理的二次筛选,我们确定了 55 种能够有效且选择性地抑制线粒体转录的化合物,它们在细胞培养中也具有活性。我们的方法很容易适应其他 RNA 或 DNA 聚合酶和不同的光谱检测技术。