Rajendran Megha, Dane Eric, Conley Jason, Tantama Mathew
Department of Chemistry, Purdue University, 560 Oval Drive, Box 68, West Lafayette, Indiana 47907; and.
Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, 77 Massachusetts Avenue, 76-211, Cambridge, Massachusetts 02139.
Biol Bull. 2016 Aug;231(1):73-84. doi: 10.1086/689592.
Adenosine triphosphate (ATP) is a universal mediator of metabolism and signaling across unicellular and multicellular species. There is a fundamental interdependence between the dynamics of ATP and the physiology that occurs inside and outside the cell. Characterizing and understanding ATP dynamics provide valuable mechanistic insight into processes that range from neurotransmission to the chemotaxis of immune cells. Therefore, we require the methodology to interrogate both temporal and spatial components of ATP dynamics from the subcellular to the organismal levels in live specimens. Over the last several decades, a number of molecular probes that are specific to ATP have been developed. These probes have been combined with imaging approaches, particularly optical microscopy, to enable qualitative and quantitative detection of this critical molecule. In this review, we survey current examples of technologies available for visualizing ATP in living cells, and identify areas where new tools and approaches are needed to expand our capabilities.
三磷酸腺苷(ATP)是单细胞和多细胞物种新陈代谢及信号传导的通用介质。ATP动态与细胞内外发生的生理过程之间存在着根本的相互依存关系。表征和理解ATP动态为从神经传递到免疫细胞趋化性等一系列过程提供了有价值的机制性见解。因此,我们需要一种方法来研究活体标本中从亚细胞水平到机体水平的ATP动态的时间和空间成分。在过去几十年中,已经开发出了许多对ATP具有特异性的分子探针。这些探针已与成像方法,特别是光学显微镜相结合,以实现对这一关键分子的定性和定量检测。在本综述中,我们概述了目前可用于在活细胞中可视化ATP的技术实例,并确定了需要新工具和方法来扩展我们能力的领域。