Department of Molecular Design and Engineering, Graduate School of Engineering, Nagoya University, Chikusa-ku, Nagoya, 464-8603, Japan.
Institute for Molecular Science, 38 Nishigo-Naka, Myodaiji, Okazaki, 444-8585, Japan.
Angew Chem Int Ed Engl. 2017 Jan 16;56(3):791-795. doi: 10.1002/anie.201611349. Epub 2016 Dec 21.
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.
当在肽的 C 末端引入富勒烯(C )衍生物时,单手 3 螺旋六肽能够有效地被 st-PMMA 的螺旋腔包封。包封伴随着 st-PMMA 主链中诱导出与六肽相同手性的优先手性螺旋构象,形成具有独特光学活性的螺旋-螺旋结构的结晶 st-PMMA/肽-C 包合物。尽管 st-PMMA 没有末端 C 单元无法包封 3 螺旋肽,但 st-PMMA 的螺旋中空空间几乎被 C 结合的肽填充。这一结果表明,C 部分可以作为 st-PMMA 螺旋腔中特定分子和聚合物的通用分子载体,用于形成包合物,从而产生其他方法无法制备的独特超分子软材料。