Angewandte Chemie International Edition · 2014 · 65 citations · 42 references
Natural SciencesMaterials EngineeringMaterials ScienceBiomaterialsEnzymologyPolymer ChemistryEnzyme StabilityGelsHydrogelsPolymeric NanoparticlesProtein-based BiomaterialsThermostable EnzymesEnzyme Thermal StabilityProtein Thermal StabilityTemperature-responsive PolymersThermal Stabilization Of EnzymesThermal Stress ToleranceThermally Responsive HydrogelsThermo-responsive HydrogelsThermoresponsive Hydrogels
We report a new material design concept for synthetic, thermally responsive poly(N-isopropylacrylamide)-based copolymer nanoparticle (NP) hydrogels, which protect proteins from thermal stress. The NP hydrogels bind and protect a target enzyme from irreversible activity loss upon exposure to heat but "autonomously" release the enzyme upon subsequent cooling of the solution. Incorporation of the optimized amount of negatively charged and hydrophobic comonomers to the NP hydrogels was key to achieve these desired functions. As the NP hydrogels do not show a strong affinity for the enzyme at room temperature, they can remain in solution without adversely affecting enzymatic activity or they can be removed by filtration to leave the enzyme in solution. The results demonstrate the promise of this approach for improving the thermal tolerance of proteins.
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The stabilization of proteins by sucrose.
James Lee, Serge N. Timasheff · Journal of Biological Chemistry · 1981 · 1.1K citations · Full text
Conformation Changes of Proteins
Rufus Lumry, Henry Eyring · The Journal of Physical Chemistry · 1954 · 866 citations