Fabrication of porphyrin-based aggregates through modulating hexapeptide secondary conformation. (March 2021)
- Record Type:
- Journal Article
- Title:
- Fabrication of porphyrin-based aggregates through modulating hexapeptide secondary conformation. (March 2021)
- Main Title:
- Fabrication of porphyrin-based aggregates through modulating hexapeptide secondary conformation
- Authors:
- Liu, Ruihong
Liu, Dongzhi
Meng, Fancui
Li, Wei
Wang, Lichang
Zhou, Xueqin - Abstract:
- Abstract: The stacking mode of aggregates directly determines the morphology and properties of assemblies. However, how the peptide secondary confirmation affects the arrangement of artificial photosynthetic supramolecules is still ambiguous. Herein, a porphyrin-hexapeptide supramolecule TPP-Ala-Ala-MV was synthesized to investigate the effect of its secondary conformation on the stacking mode and morphology of aggregates. Nanosheets, nanospheres and nanotubes were obtained from TPP-Ala-Ala-MV at different pH conditions. It was revealed that the pH condition influences not only the aggregation of porphyrin cores, but also its secondary conformation composition. Both experimental and computational results discover that the hexapeptide α-helix conformation has the strongest intramolecular hydrogen bond interaction, whereas no intermolecular hydrogen bond forms in β-sheet conformation. The inclination to J-aggregation, as well as the weak intermolecular interaction among hexapeptide turn conformation, leads to the formation of nanosheets. The inclination to H-aggregation coupled with the strong intermolecular interaction among hexapeptide β-sheet conformations promotes the formation of a highly packed structure, resulting in aggregates of nanosphere or nanotube shape. These results pave the way for the development of artificial photosynthesis systems by regulating the aggregate structures of porphyrin-peptide supramolecular systems. Highlights: A novel porphyrin-hexapeptideAbstract: The stacking mode of aggregates directly determines the morphology and properties of assemblies. However, how the peptide secondary confirmation affects the arrangement of artificial photosynthetic supramolecules is still ambiguous. Herein, a porphyrin-hexapeptide supramolecule TPP-Ala-Ala-MV was synthesized to investigate the effect of its secondary conformation on the stacking mode and morphology of aggregates. Nanosheets, nanospheres and nanotubes were obtained from TPP-Ala-Ala-MV at different pH conditions. It was revealed that the pH condition influences not only the aggregation of porphyrin cores, but also its secondary conformation composition. Both experimental and computational results discover that the hexapeptide α-helix conformation has the strongest intramolecular hydrogen bond interaction, whereas no intermolecular hydrogen bond forms in β-sheet conformation. The inclination to J-aggregation, as well as the weak intermolecular interaction among hexapeptide turn conformation, leads to the formation of nanosheets. The inclination to H-aggregation coupled with the strong intermolecular interaction among hexapeptide β-sheet conformations promotes the formation of a highly packed structure, resulting in aggregates of nanosphere or nanotube shape. These results pave the way for the development of artificial photosynthesis systems by regulating the aggregate structures of porphyrin-peptide supramolecular systems. Highlights: A novel porphyrin-hexapeptide supramolecule was synthesized and characterized. The pH conditions can change the hexapeptide secondary conformation composition. Hexapeptide turn conformations and porphyrin J-aggregation result in nanosheets. β-Sheet hexapeptide and H-aggregated porphyrin lead to nanospheres or nanotubes. … (more)
- Is Part Of:
- Dyes and pigments. Volume 187(2021)
- Journal:
- Dyes and pigments
- Issue:
- Volume 187(2021)
- Issue Display:
- Volume 187, Issue 2021 (2021)
- Year:
- 2021
- Volume:
- 187
- Issue:
- 2021
- Issue Sort Value:
- 2021-0187-2021-0000
- Page Start:
- Page End:
- Publication Date:
- 2021-03
- Subjects:
- Artificial photosynthesis system -- Self-assembly -- Peptide -- Secondary conformation
Dyes and dyeing -- Periodicals
Pigments -- Periodicals
667.2 - Journal URLs:
- http://www.sciencedirect.com/science/journal/01437208 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.dyepig.2021.109135 ↗
- Languages:
- English
- ISSNs:
- 0143-7208
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3635.600000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 15591.xml