Journal of the American Chemical Society · 2016 · 76 citations · 30 references
Life SciencesBiochemistryMolecular BiologyEnzymologyProtein EngineeringStructure-activity RelationshipsAtp HydrolysisEnzyme FunctionEnzyme KineticsProtein StructureSupramolecular PolymersAtp DependenceAtp Hydrolysis CouplingAtp Hydrolysis MechanismEnzyme ActivityEnzyme Activity RegulationEnzyme Activity RetentionHydrolytic Enzyme Activity
Water-soluble linear polymers GumBAn (m/n = 18/6, 12/12, and 6/18) with multiple guanidinium ion (Gu(+)) and boronic acid (BA) pendants in their side chains were synthesized as ATP-responsive modulators for enzyme activity. GumBAn polymers strongly bind to the phosphate ion (PO4(-)) and 1,2-diol units of ATP via the Gu(+) and BA pendants, respectively. As only the Gu(+) pendants can be used for proteins, GumBAn is able to modulate the activity of enzymes in response to ATP. As a proof-of-concept study, we demonstrated that trypsin (Trp) can be deactivated by hybridization with GumBAn. However, upon addition of ATP, Trp was liberated to retrieve its hydrolytic activity due to a higher preference of GumBAn toward ATP than Trp. This event occurred in a much lower range of [ATP] than reported examples. Under cellular conditions, the hydrolytic activity of Trp was likewise modulated.
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A detailed examination of boronic acid–diol complexation
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ATP-triggered anticancer drug delivery
Ran Mo, Tianyue Jiang, Rocco DiSanto et al. · Nature Communications · 2014 · 676 citations · Full text
Medicine, Oncology, Pharmacology +12