TY - JOUR
T1 - Thermoresponsive Protein-Engineered Coiled-Coil Hydrogel for Sustained Small Molecule Release
AU - Hill, Lindsay K.
AU - Meleties, Michael
AU - Katyal, Priya
AU - Xie, Xuan
AU - Delgado-Fukushima, Erika
AU - Jihad, Teeba
AU - Liu, Che Fu
AU - O'Neill, Sean
AU - Tu, Raymond S.
AU - Renfrew, P. Douglas
AU - Bonneau, Richard
AU - Wadghiri, Youssef Z.
AU - Montclare, Jin Kim
N1 - Funding Information:
This work was supported by NSF-DMREF under Award Number DMR 1728858 and NSF-MRSEC Program under Award Number DMR 142007.
Funding Information:
The authors thank Dr. Jeffrey F. Morris and Omer Sedes of the Chemical Engineering department at The City College of New York for their assistance with rheology experiments as well as Dr. Ken Dill from the Laufer Center for Physical and Quantitative Biology at Stony Brook University for helpful insight into the UCST. The authors also thank Andrew Olsen for his assistance in microrheology experiments and Dr. César A. Berrı́os-Otero for his assistance in data processing. This research used resources of the Center for Functional Nanomaterials, which is a U.S. DOE Office of Science Facility, at the Brookhaven National Laboratory under Contract No. DE-SC0012704 for TEM measurements. SEM and ATR-FTIR experiments were performed at the NYU Chemistry Department Shared Instrument Facility. This work was also supported in part through the NYU IT High Performance Computing resources, services, and staff expertize.
Publisher Copyright:
Copyright © 2019 American Chemical Society.
PY - 2019/9/9
Y1 - 2019/9/9
N2 - Thermoresponsive hydrogels are used for an array of biomedical applications. Lower critical solution temperature-type hydrogels have been observed in nature and extensively studied in comparison to upper critical solution temperature (UCST)-type hydrogels. Of the limited protein-based UCST-type hydrogels reported, none have been composed of a single coiled-coil domain. Here, we describe a biosynthesized homopentameric coiled-coil protein capable of demonstrating a UCST. Microscopy and structural analysis reveal that the hydrogel is stabilized by molecular entanglement of protein nanofibers, creating a porous matrix capable of binding the small hydrophobic molecule, curcumin. Curcumin binding increases the α-helical structure, fiber entanglement, mechanical integrity, and thermostability, resulting in sustained drug release at physiological temperature. This work provides the first example of a thermoresponsive hydrogel comprised of a single coiled-coil protein domain that can be used as a vehicle for sustained release and, by demonstrating UCST-type behavior, shows promise in forging a relationship between coiled-coil protein-phase behavior and that of synthetic polymer systems.
AB - Thermoresponsive hydrogels are used for an array of biomedical applications. Lower critical solution temperature-type hydrogels have been observed in nature and extensively studied in comparison to upper critical solution temperature (UCST)-type hydrogels. Of the limited protein-based UCST-type hydrogels reported, none have been composed of a single coiled-coil domain. Here, we describe a biosynthesized homopentameric coiled-coil protein capable of demonstrating a UCST. Microscopy and structural analysis reveal that the hydrogel is stabilized by molecular entanglement of protein nanofibers, creating a porous matrix capable of binding the small hydrophobic molecule, curcumin. Curcumin binding increases the α-helical structure, fiber entanglement, mechanical integrity, and thermostability, resulting in sustained drug release at physiological temperature. This work provides the first example of a thermoresponsive hydrogel comprised of a single coiled-coil protein domain that can be used as a vehicle for sustained release and, by demonstrating UCST-type behavior, shows promise in forging a relationship between coiled-coil protein-phase behavior and that of synthetic polymer systems.
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U2 - 10.1021/acs.biomac.9b00107
DO - 10.1021/acs.biomac.9b00107
M3 - Article
C2 - 31356057
AN - SCOPUS:85071733552
SN - 1525-7797
VL - 20
SP - 3340
EP - 3351
JO - Biomacromolecules
JF - Biomacromolecules
IS - 9
ER -