Department of Chemical Biology, Max Planck Institute for Medical Research, Heidelberg, Germany; Heidelberg University, Heidelberg, Germany.
Novartis Biomedical Research, Discovery Science, Basel, Switzerland.
Cell Chem Biol. 2024 Aug 15;31(8):1529-1541.e12. doi: 10.1016/j.chembiol.2024.05.002. Epub 2024 May 27.
Aspartate is crucial for nucleotide synthesis, ammonia detoxification, and maintaining redox balance via the malate-aspartate-shuttle (MAS). To disentangle these multiple roles of aspartate metabolism, tools are required that measure aspartate concentrations in real time and in live cells. We introduce AspSnFR, a genetically encoded green fluorescent biosensor for intracellular aspartate, engineered through displaying and screening biosensor libraries on mammalian cells. In live cells, AspSnFR is able to precisely and quantitatively measure cytosolic aspartate concentrations and dissect its production from glutamine. Combining high-content imaging of AspSnFR with pharmacological perturbations exposes differences in metabolic vulnerabilities of aspartate levels based on nutrient availability. Further, AspSnFR facilitates tracking of aspartate export from mitochondria through SLC25A12, the MAS' key transporter. We show that SLC25A12 is a rapidly responding and direct route to couple Ca signaling with mitochondrial aspartate export. This establishes SLC25A12 as a crucial link between cellular signaling, mitochondrial respiration, and metabolism.
天冬氨酸对于核苷酸合成、氨解毒以及通过苹果酸-天冬氨酸穿梭(MAS)维持氧化还原平衡至关重要。为了厘清天冬氨酸代谢的这些多重作用,需要能够实时且在活细胞中测量天冬氨酸浓度的工具。我们引入了 AspSnFR,这是一种用于细胞内天冬氨酸的基因编码绿色荧光生物传感器,通过在哺乳动物细胞上展示和筛选生物传感器文库来设计。在活细胞中,AspSnFR 能够精确和定量地测量细胞质中天冬氨酸的浓度,并从谷氨酰胺中剖析其产生过程。将 AspSnFR 的高内涵成像与药理学扰动相结合,根据营养物质的可用性揭示了天冬氨酸水平代谢脆弱性的差异。此外,AspSnFR 有助于通过 SLC25A12(MAS 的关键转运蛋白)追踪线粒体中天冬氨酸的输出。我们表明,SLC25A12 是一种快速响应的直接途径,可将 Ca 信号与线粒体天冬氨酸输出偶联。这确立了 SLC25A12 作为细胞信号转导、线粒体呼吸和代谢之间的关键联系。