Department of Physiology, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA, 90095-1751, USA.
Koniku Inc., 740 Heinz Avenue, Berkeley, CA, 94710, USA.
Nat Commun. 2019 Feb 12;10(1):711. doi: 10.1038/s41467-019-08441-5.
Adenosine 5' triphosphate (ATP) is a universal intracellular energy source and an evolutionarily ancient, ubiquitous extracellular signal in diverse species. Here, we report the generation and characterization of single-wavelength genetically encoded fluorescent sensors (iATPSnFRs) for imaging extracellular and cytosolic ATP from insertion of circularly permuted superfolder GFP into the epsilon subunit of FF-ATPase from Bacillus PS3. On the cell surface and within the cytosol, iATPSnFR responds to relevant ATP concentrations (30 μM to 3 mM) with fast increases in fluorescence. iATPSnFRs can be genetically targeted to specific cell types and sub-cellular compartments, imaged with standard light microscopes, do not respond to other nucleotides and nucleosides, and when fused with a red fluorescent protein function as ratiometric indicators. After careful consideration of their modest pH sensitivity, iATPSnFRs represent promising reagents for imaging ATP in the extracellular space and within cells during a variety of settings, and for further application-specific refinements.
三磷酸腺苷(ATP)是一种通用的细胞内能量来源,也是一种在不同物种中普遍存在的进化古老的细胞外信号。在这里,我们报告了单波长基因编码荧光传感器(iATPSnFRs)的产生和特性,用于从 Bacillus PS3 的 FF-ATPase 的ε亚基插入环状排列的超折叠 GFP 来成像细胞外和细胞内的 ATP。在细胞表面和细胞内,iATPSnFR 对相关 ATP 浓度(30μM 至 3mM)快速增加荧光。iATPSnFR 可以通过基因靶向特定的细胞类型和亚细胞区室,用标准显微镜成像,不响应其他核苷酸和核苷,并且当与红色荧光蛋白融合时可以作为比率型指示剂。在仔细考虑了它们适度的 pH 敏感性后,iATPSnFR 代表了在各种环境下成像细胞外空间和细胞内 ATP 的有前途的试剂,并且可以进一步进行特定应用的改进。