HHMI, Ashburn, VA 20147.
Department of Biochemistry, Weill Cornell Medicine, New York, NY 10065.
Proc Natl Acad Sci U S A. 2024 May 21;121(21):e2314604121. doi: 10.1073/pnas.2314604121. Epub 2024 May 15.
We developed a significantly improved genetically encoded quantitative adenosine triphosphate (ATP) sensor to provide real-time dynamics of ATP levels in subcellular compartments. iATPSnFR2 is a variant of iATPSnFR1, a previously developed sensor that has circularly permuted superfolder green fluorescent protein (GFP) inserted between the ATP-binding helices of the -subunit of a bacterial F-F ATPase. Optimizing the linkers joining the two domains resulted in a ~fivefold to sixfold improvement in the dynamic range compared to the previous-generation sensor, with excellent discrimination against other analytes, and affinity variants varying from 4 µM to 500 µM. A chimeric version of this sensor fused to either the HaloTag protein or a suitable spectrally separated fluorescent protein provides an optional ratiometric readout allowing comparisons of ATP across cellular regions. Subcellular targeting the sensor to nerve terminals reveals previously uncharacterized single-synapse metabolic signatures, while targeting to the mitochondrial matrix allowed direct quantitative probing of oxidative phosphorylation dynamics.
我们开发了一种经过显著改进的基因编码定量三磷酸腺苷(ATP)传感器,以提供细胞区室中 ATP 水平的实时动态。iATPSnFR2 是之前开发的传感器 iATPSnFR1 的变体,该传感器具有环状排列的超折叠绿色荧光蛋白(GFP)插入细菌 F-F ATP 酶的 -亚基的 ATP 结合螺旋之间。优化连接两个结构域的接头与上一代传感器相比,动态范围提高了约五倍到六倍,对其他分析物具有出色的区分能力,亲和变体的范围从 4µM 到 500µM。该传感器的嵌合版本与 HaloTag 蛋白或合适的光谱分离荧光蛋白融合,提供了可选的比率读数,允许在细胞区域之间比较 ATP。将传感器亚细胞靶向神经末梢揭示了以前未表征的单个突触代谢特征,而将其靶向线粒体基质则允许直接定量探测氧化磷酸化动力学。