- Nanoscale IR spectroscopy confirmed that alpha-helical secondary formation of PBLG was unaffected by the presence of pi-conjugated polymer chains
- PBLG self-assembly thermoreversible gels with long-range ordered structures provides a foundation for the design of biocompatible materials
- Results offer new opportunities to harness the propensity of polypeptide assembly into interconnected fibrillary structures to control the organization of semiconducting polymers, and explores hybrid gels as active materials in bioelectronics
nanoIR | polypeptides | semiconducting polymers | self-assembly | P3HT | PBLG | toluene | thermoreversible gel
C. Rosu, C. Tassone, P. Chu, P. Balding, A. Gorman, J. Hernandez, M. Hawkridge, A. Roy, I. Negulescu, P. Russo, and E. Reichmanis
Abstract information is provided in the full text.
AFM-IR of dry PBLG/toluene gel showing the α-helical structure of the polypeptide and AFM-IR of dry G2f.