Chirality Inversion upon Coassembly of Stereoisomeric Short Peptides with Like-Handedness

Despite numerous reports devoted to chirality inversion during the self-assembly of single chiral components, chirality inversion in the coassembly of two or more chiral components remains largely unexplored. Here we report the supramolecular chirality inversion via the coassembly of the two different stereoisomers of a minimalistic amphiphilic I<sub>3</sub>K sequence with like-handedness in their self-sorting assembly. The coassembled nanofibrils exhibit noticeable helix inversion in a wide range of mixing ratios, compared to individual peptide nanofibrils. Theoretical simulations reveal that to facilitate the interstrand H-bonding between isomeric β-strands within a mixed β-sheet, those with a homochiral backbone will undergo chirality inversion due to their structural flexibility. The inverted strands with two heterogeneous interfaces within the sheet typically display larger twisting degrees and are responsible for inducing helix inversion of the sheet and final β-sheet nanofibrils, and thus, helix inversion of the final nanofibrils can be regulated by tuning the ratio of the two components. This study lays a foundation for manipulating the suprastructure chirality of peptide bionanomaterials through coassembly.

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Publication Details

Journal
ACS Nano
Published
2025-04-21
DOI
https://doi.org/10.1021/acsnano.5c02425
Citations
5
Primary Topic
Chemical Synthesis and Analysis
Type
article
Field-Weighted Citation Impact
4.03

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article

Chirality Inversion upon Coassembly of Stereoisomeric Short Peptides with Like-Handedness

Zhenhua Xie, Xinfeng Ju, Feng Zhou, Yuanhao Jiang et al.
5 citations
ACS Nano
Chemical Synthesis and Analysis
4.03
article

Chirality Inversion upon Coassembly of Stereoisomeric Short Peptides with Like-Handedness

Zhenhua Xie, Xinfeng Ju, Feng Zhou, Yuanhao Jiang, Jian R. Lu, Yurong Zhao, Kai Qi, Yubin Ke, Muhan Wang, Xuzhi Hu, Kai Tao, Hai Long Xu, Jiqian Wang, Yan Wang, Hua He, Henghao Yu, Kenneth Alston
article en
5 citations

Abstract

Despite numerous reports devoted to chirality inversion during the self-assembly of single chiral components, chirality inversion in the coassembly of two or more chiral components remains largely unexplored. Here we report the supramolecular chirality inversion via the coassembly of the two different stereoisomers of a minimalistic amphiphilic I<sub>3</sub>K sequence with like-handedness in their self-sorting assembly. The coassembled nanofibrils exhibit noticeable helix inversion in a wide range of mixing ratios, compared to individual peptide nanofibrils. Theoretical simulations reveal that to facilitate the interstrand H-bonding between isomeric β-strands within a mixed β-sheet, those with a homochiral backbone will undergo chirality inversion due to their structural flexibility. The inverted strands with two heterogeneous interfaces within the sheet typically display larger twisting degrees and are responsible for inducing helix inversion of the sheet and final β-sheet nanofibrils, and thus, helix inversion of the final nanofibrils can be regulated by tuning the ratio of the two components. This study lays a foundation for manipulating the suprastructure chirality of peptide bionanomaterials through coassembly.

ACS NanoVol. 19(17)
Chinese Academy of Sciences (CN), University of Manchester (GB), Lanzhou Institute of Chemical Physics (CN), China Spallation Neutron Source (CN), Astronomy and Space (AU), China University of Petroleum, East China (CN), Spallation Neutron Source, Qingdao University of Technology (CN), Zhejiang University (CN)
AstraZeneca, National Natural Science Foundation of China, Biotechnology and Biological Sciences Research Council, Innovate UK
Openalex Percentile: Top 6%
Chemical Synthesis and Analysis
4.03
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