Optical control of protein phosphatase function

• Published in: Nature communications 2019-09, Vol.10 (1), p.4384-10, Article 4384
• Main Authors: Courtney, Taylor M., Deiters, Alexander
• Format: Article
• Language: English
• Subjects: 13/106; 13/95; 14/35; 631/1647/2253; 631/92/458/1733; 631/92/552; 631/92/612; 631/92/612/1246; 82/80; 96/63; Active control; Catalysis; Catalytic activity; Cell cycle; Cellular stress response; Dual Specificity Phosphatase 6 - chemistry; Dual Specificity Phosphatase 6 - genetics; Dual Specificity Phosphatase 6 - metabolism; Embryogenesis; Embryonic growth stage; Enzyme Activation - radiation effects; Extracellular signal-regulated kinase; Genetic code; HEK293 Cells; Homeostasis; Humanities and Social Sciences; Humans; Kinases; Luminescent Proteins - chemistry; Luminescent Proteins - genetics; Luminescent Proteins - metabolism; Lysine; Microscopy, Fluorescence; multidisciplinary; Mutation; Nuclear transport; Optical control; Optogenetics - methods; Phosphatase; Protein interaction; Protein phosphatase; Proteins; Science; Science (multidisciplinary); Substrates; Time-Lapse Imaging - methods; Translocation; Ultraviolet Rays
• ISSN: 2041-1723; 2041-1723
• DOI: 10.1038/s41467-019-12260-z

Protein phosphatases are involved in embryonic development, metabolic homeostasis, stress response, cell cycle transitions, and many other essential biological mechanisms. Unlike kinases, protein phosphatases remain understudied and less characterized. Traditional genetic and biochemical methods have contributed significantly to our understanding; however, these methodologies lack precise and acute spatiotemporal control. Here, we report the development of a light-activated protein phosphatase, the dual specificity phosphatase 6 (DUSP6 or MKP3). Through genetic code expansion, MKP3 is placed under optical control via two different approaches: (i) incorporation of a caged cysteine into the active site for controlling catalytic activity and (ii) incorporation of a caged lysine into the kinase interaction motif for controlling the protein-protein interaction between the phosphatase and its substrate. Both strategies are expected to be applicable to the engineering of a wide range of light-activated phosphatases. Applying the optogenetically controlled MKP3 in conjunction with live cell reporters, we discover that ERK nuclear translocation is regulated in a graded manner in response to increasing MKP3 activity. Protein phosphatases play an essential role in signal transduction, but are understudied due to the difficulties in detecting phosphate removal and the lack of good inhibitors. Here the authors develop a light-activated protein phosphatase using photocaged, unnatural amino acids and use it to study ERK nuclear translocation.