三磷酸腺苷
绿色荧光蛋白
荧光
线粒体基质
费斯特共振能量转移
ATP酶
生物物理学
蛋白质亚单位
质子泵
生物化学
生物
细胞生物学
化学
胞浆
基因
酶
物理
量子力学
作者
Jonathan S. Marvin,Alexandros C. Kokotos,Mukesh Kumar,Camila Pulido,Ariana N. Tkachuk,J. Yao,Timothy A. Brown,Timothy A. Ryan
标识
DOI:10.1073/pnas.2314604121
摘要
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 ε -subunit of a bacterial F 0 -F 1 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.
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