Engineering Elastin-Like Polypeptide-Poly(ethylene glycol) Multiblock Physical Networks
Abstract
Hybrids of protein biopolymers and synthetic polymers are a promising new class of soft materials, as the advantages of each component can be complementary. A recombinant elastin-like polypeptide (ELP) was conjugated to poly(ethylene glycol) (PEG) by macromolecular coupling in solution to form multiblock ELP-PEG copolymers. The hydrated copolymer preserved the thermoresponsive properties from the ELP block and formed hydrogels with different transition temperatures depending on salt concentration. Small angle scattering indicates that the copolymer hydrogels form sphere-like aggregates with a “fuzzy” interface, while the films form a fractal network of nanoscale aggregates. Here, the use of solutions with different salt concentrations to prepare the hydrogels was found to influence the transition temperature, the mechanical properties, and the size of the nanoscale structure of the hydrogel without changing the secondary structure of the ELP. The salt variation and the addition of a plasticizer also affected the nanoscale structure and the mechanical characteristics of the films.
- Authors:
-
- Univ. of Minho, Guimarães (Portugal)
- Massachusetts Inst. of Technology (MIT), Cambridge, MA (United States)
- Publication Date:
- Research Org.:
- Argonne National Laboratory (ANL), Argonne, IL (United States)
- Sponsoring Org.:
- National Science Foundation (NSF)
- OSTI Identifier:
- 1437484
- Resource Type:
- Accepted Manuscript
- Journal Name:
- Biomacromolecules
- Additional Journal Information:
- Journal Volume: 19; Journal Issue: 2; Journal ID: ISSN 1525-7797
- Publisher:
- American Chemical Society
- Country of Publication:
- United States
- Language:
- ENGLISH
- Subject:
- 59 BASIC BIOLOGICAL SCIENCES; thin films; amides; peptides and proteins; copolymers; hydrogels; PEG; ELP; physical networks
Citation Formats
Araújo, Andreia, Olsen, Bradley D., and Machado, Ana Vera. Engineering Elastin-Like Polypeptide-Poly(ethylene glycol) Multiblock Physical Networks. United States: N. p., 2017.
Web. doi:10.1021/acs.biomac.7b01424.
Araújo, Andreia, Olsen, Bradley D., & Machado, Ana Vera. Engineering Elastin-Like Polypeptide-Poly(ethylene glycol) Multiblock Physical Networks. United States. https://doi.org/10.1021/acs.biomac.7b01424
Araújo, Andreia, Olsen, Bradley D., and Machado, Ana Vera. Mon .
"Engineering Elastin-Like Polypeptide-Poly(ethylene glycol) Multiblock Physical Networks". United States. https://doi.org/10.1021/acs.biomac.7b01424. https://www.osti.gov/servlets/purl/1437484.
@article{osti_1437484,
title = {Engineering Elastin-Like Polypeptide-Poly(ethylene glycol) Multiblock Physical Networks},
author = {Araújo, Andreia and Olsen, Bradley D. and Machado, Ana Vera},
abstractNote = {Hybrids of protein biopolymers and synthetic polymers are a promising new class of soft materials, as the advantages of each component can be complementary. A recombinant elastin-like polypeptide (ELP) was conjugated to poly(ethylene glycol) (PEG) by macromolecular coupling in solution to form multiblock ELP-PEG copolymers. The hydrated copolymer preserved the thermoresponsive properties from the ELP block and formed hydrogels with different transition temperatures depending on salt concentration. Small angle scattering indicates that the copolymer hydrogels form sphere-like aggregates with a “fuzzy” interface, while the films form a fractal network of nanoscale aggregates. Here, the use of solutions with different salt concentrations to prepare the hydrogels was found to influence the transition temperature, the mechanical properties, and the size of the nanoscale structure of the hydrogel without changing the secondary structure of the ELP. The salt variation and the addition of a plasticizer also affected the nanoscale structure and the mechanical characteristics of the films.},
doi = {10.1021/acs.biomac.7b01424},
journal = {Biomacromolecules},
number = 2,
volume = 19,
place = {United States},
year = {Mon Dec 18 00:00:00 EST 2017},
month = {Mon Dec 18 00:00:00 EST 2017}
}
Web of Science
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