“Helix‐in‐Helix” Superstructure Formation through Encapsulation of Fullerene‐Bound Helical Peptides within a Helical Poly(methyl methacrylate) Cavity
A one‐handed 310‐helical hexapeptide is efficiently encapsulated within the helical cavity of st‐PMMA when a fullerene (C60) derivative is introduced at the C‐terminal end of the peptide. The encapsulation is accompanied by induction of a preferred‐handed helical conformation in the st‐PMMA backbone...
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Published in | Angewandte Chemie International Edition Vol. 56; no. 3; pp. 791 - 795 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
WEINHEIM
Wiley
16.01.2017
Wiley Subscription Services, Inc John Wiley and Sons Inc |
Edition | International ed. in English |
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Abstract | A one‐handed 310‐helical hexapeptide is efficiently encapsulated within the helical cavity of st‐PMMA when a fullerene (C60) derivative is introduced at the C‐terminal end of the peptide. The encapsulation is accompanied by induction of a preferred‐handed helical conformation in the st‐PMMA backbone with the same‐handedness as that of the hexapeptide to form a crystalline st‐PMMA/peptide‐C60 inclusion complex with a unique optically active helix‐in‐helix structure. Although the st‐PMMA is unable to encapsulate the 310‐helical peptide without the terminal C60 unit, the helical hollow space of the st‐PMMA is almost filled by the C60‐bound peptides. This result suggests that the C60 moiety can serve as a versatile molecular carrier of specific molecules and polymers in the helical cavity of the st‐PMMA for the formation of an inclusion complex, thus producing unique supramolecular soft materials that cannot be prepared by other methods.
One hand twisting: A one‐handed helical peptide bearing a C60 moiety at one end is encapsulated within the helical cavity of syndiotactic poly(methyl methacrylate) (st‐PMMA) as a result of the C60 moiety which strongly interacts with the st‐PMMA cavity. This encapsulation induces the st‐PMMA backbone to adopt the same handedness as the encapsulated peptides. |
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AbstractList | A one‐handed 310‐helical hexapeptide is efficiently encapsulated within the helical cavity of st‐PMMA when a fullerene (C60) derivative is introduced at the C‐terminal end of the peptide. The encapsulation is accompanied by induction of a preferred‐handed helical conformation in the st‐PMMA backbone with the same‐handedness as that of the hexapeptide to form a crystalline st‐PMMA/peptide‐C60 inclusion complex with a unique optically active helix‐in‐helix structure. Although the st‐PMMA is unable to encapsulate the 310‐helical peptide without the terminal C60 unit, the helical hollow space of the st‐PMMA is almost filled by the C60‐bound peptides. This result suggests that the C60 moiety can serve as a versatile molecular carrier of specific molecules and polymers in the helical cavity of the st‐PMMA for the formation of an inclusion complex, thus producing unique supramolecular soft materials that cannot be prepared by other methods. A one‐handed 3 10 ‐helical hexapeptide is efficiently encapsulated within the helical cavity of st‐PMMA when a fullerene (C 60 ) derivative is introduced at the C‐terminal end of the peptide. The encapsulation is accompanied by induction of a preferred‐handed helical conformation in the st‐PMMA backbone with the same‐handedness as that of the hexapeptide to form a crystalline st‐PMMA/peptide‐C 60 inclusion complex with a unique optically active helix‐in‐helix structure. Although the st‐PMMA is unable to encapsulate the 3 10 ‐helical peptide without the terminal C 60 unit, the helical hollow space of the st‐PMMA is almost filled by the C 60 ‐bound peptides. This result suggests that the C 60 moiety can serve as a versatile molecular carrier of specific molecules and polymers in the helical cavity of the st‐PMMA for the formation of an inclusion complex, thus producing unique supramolecular soft materials that cannot be prepared by other methods. A one-handed 3 -helical hexapeptide is efficiently encapsulated within the helical cavity of st-PMMA when a fullerene (C ) derivative is introduced at the C-terminal end of the peptide. The encapsulation is accompanied by induction of a preferred-handed helical conformation in the st-PMMA backbone with the same-handedness as that of the hexapeptide to form a crystalline st-PMMA/peptide-C inclusion complex with a unique optically active helix-in-helix structure. Although the st-PMMA is unable to encapsulate the 3 -helical peptide without the terminal C unit, the helical hollow space of the st-PMMA is almost filled by the C -bound peptides. This result suggests that the C moiety can serve as a versatile molecular carrier of specific molecules and polymers in the helical cavity of the st-PMMA for the formation of an inclusion complex, thus producing unique supramolecular soft materials that cannot be prepared by other methods. Abstract A one‐handed 3 10 ‐helical hexapeptide is efficiently encapsulated within the helical cavity of st‐PMMA when a fullerene (C 60 ) derivative is introduced at the C‐terminal end of the peptide. The encapsulation is accompanied by induction of a preferred‐handed helical conformation in the st‐PMMA backbone with the same‐handedness as that of the hexapeptide to form a crystalline st‐PMMA/peptide‐C 60 inclusion complex with a unique optically active helix‐in‐helix structure. Although the st‐PMMA is unable to encapsulate the 3 10 ‐helical peptide without the terminal C 60 unit, the helical hollow space of the st‐PMMA is almost filled by the C 60 ‐bound peptides. This result suggests that the C 60 moiety can serve as a versatile molecular carrier of specific molecules and polymers in the helical cavity of the st‐PMMA for the formation of an inclusion complex, thus producing unique supramolecular soft materials that cannot be prepared by other methods. A one‐handed 310‐helical hexapeptide is efficiently encapsulated within the helical cavity of st‐PMMA when a fullerene (C60) derivative is introduced at the C‐terminal end of the peptide. The encapsulation is accompanied by induction of a preferred‐handed helical conformation in the st‐PMMA backbone with the same‐handedness as that of the hexapeptide to form a crystalline st‐PMMA/peptide‐C60 inclusion complex with a unique optically active helix‐in‐helix structure. Although the st‐PMMA is unable to encapsulate the 310‐helical peptide without the terminal C60 unit, the helical hollow space of the st‐PMMA is almost filled by the C60‐bound peptides. This result suggests that the C60 moiety can serve as a versatile molecular carrier of specific molecules and polymers in the helical cavity of the st‐PMMA for the formation of an inclusion complex, thus producing unique supramolecular soft materials that cannot be prepared by other methods. One hand twisting: A one‐handed helical peptide bearing a C60 moiety at one end is encapsulated within the helical cavity of syndiotactic poly(methyl methacrylate) (st‐PMMA) as a result of the C60 moiety which strongly interacts with the st‐PMMA cavity. This encapsulation induces the st‐PMMA backbone to adopt the same handedness as the encapsulated peptides. A one-handed 3(10)-helical hexapeptide is efficiently encapsulated within the helical cavity of st-PMMA when a fullerene (C-60) derivative is introduced at the C-terminal end of the peptide. The encapsulation is accompanied by induction of a preferred-handed helical conformation in the st-PMMA backbone with the same-handedness as that of the hexapeptide to form a crystalline st-PMMA/peptide-C-60 inclusion complex with a unique optically active helix-in-helix structure. Although the st-PMMA is unable to encapsulate the 3(10)-helical peptide without the terminal C-60 unit, the helical hollow space of the st-PMMA is almost filled by the C-60-bound peptides. This result suggests that the C-60 moiety can serve as a versatile molecular carrier of specific molecules and polymers in the helical cavity of the st-PMMA for the formation of an inclusion complex, thus producing unique supramolecular soft materials that cannot be prepared by other methods. |
Author | Nishimura, Katsuyuki Yashima, Eiji Iwata, Yoshiaki Mamiya, Fumihiko Ousaka, Naoki |
AuthorAffiliation | 1 Department of Molecular Design and Engineering Graduate School of Engineering Nagoya University Chikusa-ku Nagoya 464-8603 Japan 2 Institute for Molecular Science 38 Nishigo-Naka, Myodaiji Okazaki 444-8585 Japan |
AuthorAffiliation_xml | – name: 1 Department of Molecular Design and Engineering Graduate School of Engineering Nagoya University Chikusa-ku Nagoya 464-8603 Japan – name: 2 Institute for Molecular Science 38 Nishigo-Naka, Myodaiji Okazaki 444-8585 Japan |
Author_xml | – sequence: 1 givenname: Naoki surname: Ousaka fullname: Ousaka, Naoki organization: Nagoya University – sequence: 2 givenname: Fumihiko surname: Mamiya fullname: Mamiya, Fumihiko organization: Nagoya University – sequence: 3 givenname: Yoshiaki surname: Iwata fullname: Iwata, Yoshiaki organization: Nagoya University – sequence: 4 givenname: Katsuyuki surname: Nishimura fullname: Nishimura, Katsuyuki organization: Institute for Molecular Science – sequence: 5 givenname: Eiji surname: Yashima fullname: Yashima, Eiji email: yashima@apchem.nagoya-u.ac.jp organization: Nagoya University |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/28000337$$D View this record in MEDLINE/PubMed |
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Keywords | POLYMERS chirality helical structures INCLUSION COMPLEXES peptides fullerenes CONFORMATION ASSEMBLIES MEMORY FOLDAMERS NANOTUBES CHIRAL AMPLIFICATION C-60 supramolecular chemistry |
Language | English |
License | Attribution-NonCommercial 2016 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
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Snippet | A one‐handed 310‐helical hexapeptide is efficiently encapsulated within the helical cavity of st‐PMMA when a fullerene (C60) derivative is introduced at the... A one-handed 3(10)-helical hexapeptide is efficiently encapsulated within the helical cavity of st-PMMA when a fullerene (C-60) derivative is introduced at the... A one-handed 3 -helical hexapeptide is efficiently encapsulated within the helical cavity of st-PMMA when a fullerene (C ) derivative is introduced at the... Abstract A one‐handed 3 10 ‐helical hexapeptide is efficiently encapsulated within the helical cavity of st‐PMMA when a fullerene (C 60 ) derivative is... A one-handed 310-helical hexapeptide is efficiently encapsulated within the helical cavity of st-PMMA when a fullerene (C60) derivative is introduced at the... A one‐handed 3 10 ‐helical hexapeptide is efficiently encapsulated within the helical cavity of st‐PMMA when a fullerene (C 60 ) derivative is introduced at... |
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SubjectTerms | Buckminsterfullerene Chemistry Chemistry, Multidisciplinary chirality Communication Communications Conformation Encapsulation Fullerenes Fullerenes - chemistry Handedness helical structures Inclusion complexes Macromolecular Substances - chemical synthesis Macromolecular Substances - chemistry Molecular Structure Optical activity Peptides Peptides - chemical synthesis Peptides - chemistry Physical Sciences Polymers Polymethyl methacrylate Polymethyl Methacrylate - chemistry Polymethylmethacrylate Science & Technology Superstructures supramolecular chemistry |
Title | “Helix‐in‐Helix” Superstructure Formation through Encapsulation of Fullerene‐Bound Helical Peptides within a Helical Poly(methyl methacrylate) Cavity |
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