Department of Medicinal Chemistry, University of Utah College of Pharmacy, Salt Lake City, UT 84112-0581, USA.
Department of Medicinal Chemistry, University of Utah College of Pharmacy, Salt Lake City, UT 84112-0581, USA.
Curr Opin Chem Biol. 2020 Aug;57:34-40. doi: 10.1016/j.cbpa.2020.04.004. Epub 2020 May 26.
The ability to visualize enzyme activity in a cell, tissue, or living organism can greatly enhance our understanding of the biological roles of that enzyme. While many aspects of cellular signaling are controlled by reversible protein phosphorylation, our understanding of the biological roles of the protein phosphatases involved is limited. Here, we provide an overview of progress toward the development of fluorescent probes that can be used to visualize the activity of protein phosphatases. Significant advances include the development of probes with visible and near-infrared (near-IR) excitation and emission profiles, which provides greater tissue and whole-animal imaging capabilities. In addition, the development of peptide-based probes has provided some selectivity for a phosphatase of interest. Key challenges involve the difficulty of achieving sufficient selectivity for an individual member of a phosphatase enzyme family and the necessity of fully validating the best probes before they can be adopted widely.
在细胞、组织或活体中可视化酶活性的能力可以极大地增强我们对该酶的生物学作用的理解。虽然细胞信号转导的许多方面受到可逆蛋白磷酸化的控制,但我们对所涉及的蛋白磷酸酶的生物学作用的理解是有限的。在这里,我们提供了一个关于开发荧光探针的进展概述,这些探针可用于可视化蛋白磷酸酶的活性。重大进展包括开发具有可见和近红外(近红外)激发和发射谱的探针,这为组织和全动物成像提供了更大的能力。此外,基于肽的探针的开发为感兴趣的磷酸酶提供了一些选择性。关键的挑战包括对磷酸酶酶家族的单个成员实现足够选择性的难度,以及在广泛采用之前必须充分验证最佳探针。