“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 inAngewandte Chemie International Edition Vol. 56; no. 3; pp. 791 - 795
Main Authors Ousaka, Naoki, Mamiya, Fumihiko, Iwata, Yoshiaki, Nishimura, Katsuyuki, Yashima, Eiji
Format Journal Article
LanguageEnglish
Published WEINHEIM Wiley 16.01.2017
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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.
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
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Issue 3
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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SSID ssj0028806
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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
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fanie.201611349
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https://www.ncbi.nlm.nih.gov/pubmed/28000337
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https://pubmed.ncbi.nlm.nih.gov/PMC5248627
Volume 56
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