Directed co-assembly of heme proteins with amphiphilic block copolymers toward functional biomolecular materials
Directed co-assembly of block copolymers and proteins/peptides may lead to hierarchically structured functional biomolecular materials. However, this requires one to synergistically direct multiple self-assembly processes. Retaining proper cofactor binding is essential to utilize many bio-motifs for...
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Sprache: | eng |
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Zusammenfassung: | Directed co-assembly of block copolymers and proteins/peptides may lead to hierarchically structured functional biomolecular materials. However, this requires one to synergistically direct multiple self-assembly processes. Retaining proper cofactor binding is essential to utilize many bio-motifs for catalytic reactions and sensing. Here, by using a heme-binding helix bundle peptide-polymer conjugate and a
holo
myoglobin-polymer conjugate as examples, we show that the simultaneous, macroscopic assembly of heme-binding proteins and diblock copolymers can be achieved in thin films without compromising protein structures, cofactor binding and enzymatic activities. To our knowledge, this is the first example of a protein/cofactor complex formed upon being co-assembled with an amphiphilic block copolymer in thin films. Molecular assembly
via
a combination of biomolecular recognition and polymer phase separation in this fashion will lead to hybrid materials combining properties of both synthetic and biological building blocks.
We report the simultaneous co-assembly of block copolymers with protein-cofactor complexes, using a combination of polymer phase separation and biomolecular recognition to generate hierarchically ordered materials. Co-assembly of block copolymers with heme proteins, using a combination of polymer phase separation and biomolecular recognition, generates hierarchically-ordered materials. |
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ISSN: | 1744-683X 1744-6848 |
DOI: | 10.1039/c0sm00817f |