Enantiomeric peptides self-assembling into fibrils with the same handedness.

IF 4.3 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
YongFang Zheng, ShiXian Chen, KeJing Mao, Hu Zhu
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引用次数: 0

Abstract

It is widely accepted that peptides with enantiomeric configurations would self-assemble into nanostructures with opposite supramolecular chirality. However, in this work, we found that the L-peptide polyphenylalanine F10 (FFFFFFFFFF) and its enantiomer f10 displayed mirror image CD spectra, yet both self-assembled into fibers with exclusive left-handedness, a phenomenon also observed in the other two enantiomeric pairs (F9f and f9F, F5f5 and f5F5). Our work provides new insights into the relationship between the molecular chirality of peptide building blocks and the supramolecular chirality of their self-assemblies.

Abstract Image

对映体肽自组装成具有相同手性的纤维。
人们普遍认为,具有对映体构型的肽会自组装成具有相反超分子手性的纳米结构。然而,在这项研究中,我们发现 L 肽多聚苯丙氨酸 F10 (FFFFFFFFFF) 及其对映体 f10 显示出镜像 CD 光谱,但两者都能自组装成具有唯一左旋性的纤维,这一现象在其他两个对映体对(F9f 和 f9F、F5f5 和 f5F5)中也有观察到。我们的研究工作为了解肽构建模块的分子手性与其自组装的超分子手性之间的关系提供了新的视角。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Chemical Communications
Chemical Communications 化学-化学综合
CiteScore
8.60
自引率
4.10%
发文量
2705
审稿时长
1.4 months
期刊介绍: ChemComm (Chemical Communications) is renowned as the fastest publisher of articles providing information on new avenues of research, drawn from all the world''s major areas of chemical research.
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