AspSnFR:用于实时监测活细胞中天冬氨酸的基因编码生物传感器

IF 6.6 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Cell Chemical Biology Pub Date : 2024-08-15 DOI:10.1016/j.chembiol.2024.05.002
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引用次数: 0

摘要

天冬氨酸对核苷酸合成、氨解毒以及通过苹果酸-天冬氨酸转换器(MAS)维持氧化还原平衡至关重要。要厘清天冬氨酸代谢的这些多重作用,需要能在活细胞中实时测量天冬氨酸浓度的工具。我们介绍的 AspSnFR 是一种经基因编码的细胞内天冬氨酸绿色荧光生物传感器,它是通过在哺乳动物细胞上显示和筛选生物传感器文库而设计出来的。在活细胞中,AspSnFR 能够精确地定量测量细胞膜天冬氨酸的浓度,并从谷氨酰胺中分解出天冬氨酸。将 AspSnFR 的高含量成像与药理学扰动相结合,可揭示天冬氨酸水平在营养物质可用性基础上的代谢脆弱性差异。此外,AspSnFR 还有助于跟踪天门冬氨酸通过 MAS 的关键转运体 SLC25A12 从线粒体输出的情况。我们的研究表明,SLC25A12 是将 Ca2+ 信号与线粒体天冬氨酸输出结合起来的快速反应和直接途径。这证明 SLC25A12 是细胞信号、线粒体呼吸和新陈代谢之间的关键纽带。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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AspSnFR: A genetically encoded biosensor for real-time monitoring of aspartate in live cells

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 Ca2+ signaling with mitochondrial aspartate export. This establishes SLC25A12 as a crucial link between cellular signaling, mitochondrial respiration, and metabolism.

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来源期刊
Cell Chemical Biology
Cell Chemical Biology Biochemistry, Genetics and Molecular Biology-Molecular Medicine
CiteScore
14.70
自引率
2.30%
发文量
143
期刊介绍: Cell Chemical Biology, a Cell Press journal established in 1994 as Chemistry & Biology, focuses on publishing crucial advances in chemical biology research with broad appeal to our diverse community, spanning basic scientists to clinicians. Pioneering investigations at the chemistry-biology interface, the journal fosters collaboration between these disciplines. We encourage submissions providing significant conceptual advancements of broad interest across chemical, biological, clinical, and related fields. Particularly sought are articles utilizing chemical tools to perturb, visualize, and measure biological systems, offering unique insights into molecular mechanisms, disease biology, and therapeutics.
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