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利用基因编码荧光生物传感器监测线粒体 GTP-to-GDP 比率的动态调控。

Monitoring the Dynamic Regulation of the Mitochondrial GTP-to-GDP Ratio with a Genetically Encoded Fluorescent Biosensor.

机构信息

State Key Laboratory of Natural and Biomimetic Drugs and Department of Chemical Biology, Department of Chemical Biology, School of Pharmaceutical Sciences, Peking University, Peking University, Beijing, 100191, China.

Wellcome Centre for Human Genetics, University of Oxford, Roosevelt Dr, Headington, Oxford, OX3 7BN, UK.

出版信息

Angew Chem Int Ed Engl. 2022 Aug 15;61(33):e202201266. doi: 10.1002/anie.202201266. Epub 2022 Jul 8.

Abstract

The interconversion of guanosine triphosphate (GTP) and guanosine diphosphate (GDP) is known to be integral to a wide variety of biological cellular activities, yet to date there are no analytical methods available to directly detect the ratio of intracellular GTP to GDP. Herein, we report GRISerHR, a genetically encoded fluorescent biosensor to monitor the GTP : GDP ratio in multiple cell types and in various organelles under metabolic perturbation. Additionally, we characterized the differential mitochondrial GTP : GDP ratios resulting from genetic modulation of two isoforms of a tricarboxylic acid (TCA) cycle enzyme (succinyl-CoA synthetase; SCS-ATP and SCS-GTP) and of a phosphoenolpyruvate (PEP) cycle enzyme (PEPCK-M). Thus, our GRISerHR sensor achieves spatiotemporally precise detection of dynamic changes in the endogenous GTP : GDP ratio in living cells and can help deepen our understanding about the energy metabolic contributions of guanosine nucleotides in biology.

摘要

三磷酸鸟苷(GTP)和二磷酸鸟苷(GDP)的相互转化是许多生物细胞活动所必需的,但迄今为止,还没有可用于直接检测细胞内 GTP 与 GDP 比值的分析方法。在此,我们报告了 GRISerHR,这是一种遗传编码的荧光生物传感器,可在代谢应激下监测多种细胞类型和各种细胞器中的 GTP:GDP 比值。此外,我们还对两种三羧酸(TCA)循环酶(琥珀酰辅酶 A 合成酶;SCS-ATP 和 SCS-GTP)和磷酸烯醇丙酮酸(PEP)循环酶(PEPCK-M)的遗传调节导致的线粒体 GTP:GDP 比值进行了特征描述。因此,我们的 GRISerHR 传感器实现了对活细胞内内源性 GTP:GDP 比值的时空精确检测,并有助于加深我们对生物中鸟嘌呤核苷酸在能量代谢中的贡献的理解。

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