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Protein Engineered Triblock Polymers Composed of Two SADs: Enhanced Mechanical Properties and Binding Abilities
- Source :
- Biomacromolecules. 19:1552-1561
- Publication Year :
- 2018
- Publisher :
- American Chemical Society (ACS), 2018.
-
Abstract
- Recombinant methods have been used to engineer artificial protein triblock polymers composed of two different self-assembling domains (SADs) bearing one elastin (E) flanked by two cartilage oligomeric matrix protein coiled-coil (C) domains to generate CEC. To understand how the two C domains improve small molecule recognition and the mechanical integrity of CEC, we have constructed CL44AECL44A, which bears an impaired CL44A domain that is unstructured as a negative control. The CEC triblock polymer demonstrates increased small molecule binding and ideal elastic behavior for hydrogel formation. The negative control CL44AECL44A does not exhibit binding to small molecule and is inelastic at lower temperatures, affirming the favorable role of C domain and its helical conformation. While both CEC and CL44AECL44A assemble into micelles, CEC is more densely packed with C domains on the surface enabling the development of networks leading to hydrogel formation. Such protein engineered triblock copolymers capable ...
- Subjects :
- 0301 basic medicine
Polymers and Plastics
Amino Acid Motifs
Protein domain
Bioengineering
Plasma protein binding
Cartilage Oligomeric Matrix Protein
010402 general chemistry
01 natural sciences
Micelle
Biomaterials
03 medical and health sciences
Protein Domains
Materials Chemistry
Copolymer
Micelles
chemistry.chemical_classification
Cartilage oligomeric matrix protein
biology
Polymer
Small molecule
Elasticity
Elastin
0104 chemical sciences
030104 developmental biology
chemistry
cardiovascular system
biology.protein
Biophysics
Stress, Mechanical
Small molecule binding
Protein Binding
Subjects
Details
- ISSN :
- 15264602 and 15257797
- Volume :
- 19
- Database :
- OpenAIRE
- Journal :
- Biomacromolecules
- Accession number :
- edsair.doi.dedup.....f9a546c02c19f3aef7395c0433bdb819
- Full Text :
- https://doi.org/10.1021/acs.biomac.7b01259