Abstract
The design and synthesis of AX7574, a microcystin-derived probe for serine/threonine phosphatases, is described. A key step in the synthesis was the conjugation under basic conditions of a tetramethylrhodamine 1,3-diketone derivative to the arginine side chain present in microcystin-LR. The resulting conjugate specifically labeled the active site of protein phosphatases 1 (PP-1) with a 1:1 stoichiometry and IC50 of 4.0 nM. AX7574 was used to isolate and identify PP-1, PP-2A, PP-4, and PP-6 in Jurkat cells. Finally, AX7574 was able to record changes in the phosphatase activity levels of calyculin A treated Jurkat cells versus untreated control cells.
MeSH terms
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Drug Design*
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Enzyme Inhibitors / pharmacology
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Fluorescence
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Fluorescent Dyes
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Humans
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Inhibitory Concentration 50
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Jurkat Cells
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Kinetics
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Marine Toxins
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Mass Spectrometry
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Microcystins
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Molecular Probes / analysis*
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Molecular Probes / antagonists & inhibitors
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Molecular Probes / chemical synthesis*
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Molecular Probes / chemistry
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Molecular Structure
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Oxazoles / pharmacology
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Peptides, Cyclic / analysis*
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Peptides, Cyclic / antagonists & inhibitors
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Peptides, Cyclic / chemical synthesis*
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Peptides, Cyclic / chemistry*
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Phosphoprotein Phosphatases / analysis
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Phosphoprotein Phosphatases / metabolism*
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Proteome / drug effects
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Proteome / metabolism
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Staining and Labeling
Substances
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AX 7574
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Enzyme Inhibitors
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Fluorescent Dyes
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Marine Toxins
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Microcystins
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Molecular Probes
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Oxazoles
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Peptides, Cyclic
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Proteome
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microcystin
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calyculin A
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Phosphoprotein Phosphatases