Publication | Open Access
Mimicking Cellular Signaling Pathways within Synthetic Multicompartment Vesicles with Triggered Enzyme Activity and Induced Ion Channel Recruitment
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Citations
40
References
2019
Year
Protein SecretionEngineeringMolecular BiologyBiofabricationExtracellular MicrovesiclesCytoskeletonAnalytical UltracentrifugationCellular PhysiologyBioimagingSecretory PathwayCell SignalingMolecular ImagingBiophysicsMacromolecular AssembliesSynthetic Multicompartment VesiclesBiochemistryTriggered Enzyme ActivityIon ChannelsMembrane BiologyBiological SystemsProtein TransportAbstract Subcellular CompartmentalizationCell BiologyBiomolecular ScienceSingle-molecule DetectionBiomolecular EngineeringSignal TransductionBiomedical DiagnosticsIntracellular TraffickingCellular BiochemistryCellular Signaling PathwaysMedicine
Abstract Subcellular compartmentalization of cells, a defining characteristic of eukaryotes, is fundamental for the fine tuning of internal processes and the responding to external stimuli. Reproducing and controlling such compartmentalized hierarchical organization, responsiveness, and communication is important toward understanding biological systems and applying them to smart materials. Herein, a cellular signal transduction strategy (triggered release from subcompartments) is leveraged to develop responsive, purely artificial, polymeric multicompartment assemblies. Incorporation of responsive nanoparticles—loaded with enzymatic substrate or ion channels—as subcompartments inside micrometer‐sized polymeric vesicles (polymersomes) allowed to conduct bioinspired signaling cascades. Response of these subcompartments to an externally added stimulus is achieved and studied by using confocal laser scanning microscopy (CLSM) coupled with in situ fluorescence correlation spectroscopy (FCS). Signal triggered activity of an enzymatic reaction is demonstrated in multicompartments through recombination of compartmentalized substrate and enzyme. In parallel, a two‐step signaling cascade is achieved by triggering the recruitment of ion channels from inner subcompartments to the vesicles' membrane, inducing ion permeability, mimicking endosome‐mediated insertion of internally stored channels. This design shows remarkable versatility, robustness, and controllability, demonstrating that multicompartment polymer‐based assemblies offer an ideal scaffold for the development of complex cell‐inspired responsive systems for applications in biosensing, catalysis, and medicine.
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