Affiliation:
1. Department of Materials Science and Engineering University of Delaware Newark DE 19716 USA
2. Department of Chemistry University of Pennsylvania Philadelphia PA 19104 USA
3. Department of Biomedical Engineering University of Delaware Newark DE 19716 USA
Abstract
AbstractThermoresponsive resilin‐like polypeptides (RLPs) of various lengths were genetically fused to two different computationally designed coiled coil‐forming peptides with distinct thermal stability, to develop new strategies to assemble coiled coil peptides via temperature‐triggered phase separation of the RLP units. Their successful production in bacterial expression hosts was verified via gel electrophoresis, mass spectrometry, and amino acid analysis. Circular dichroism (CD) spectroscopy, ultraviolet‐visible (UV/Vis) turbidimetry, and dynamic light scattering (DLS) measurements confirmed the stability of the coiled coils and showed that the thermosensitive phase behavior of the RLPs was preserved in the genetically fused hybrid polypeptides. Cryogenic‐transmission electron microscopy and coarse‐grained modeling revealed that functionalizing the coiled coils with thermoresponsive RLPs leads to their thermally triggered noncovalent assembly into nanofibrillar assemblies.
Funder
Division of Materials Research
National Institutes of Health
NIST Center for Neutron Research
Basic Energy Sciences
National Science Foundation
Subject
General Chemistry,Catalysis
Cited by
6 articles.
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