Hydrophobicity‐Controlled Self‐Assembly of Supramolecular Peptide Nanotubes in Water

Polymer-conjugated peptides are attractive building blocks for the construction of new nanomaterials. However, the ability to control the self-assembly of these materials remains a major limitation to their wider utilization. Herein, we report a facile strategy to fine-tune the assembly of water-soluble hydrophilic polymer-conjugated cyclic peptides by incorporating a defined, short hydrocarbon linker between the polymer and peptide. This addition creates a well-defined hydrophobic "inner shell" that suppresses water from disrupting the organized peptide hydrogen bond network. Our approach is demonstrated using a series of cyclic peptide-linker-PDMA conjugates that were evaluated by asymmetric flow field flow fractionation, small angle neutron scattering and transmission electron microscopy. Molecular dynamics simulations were also used to show how the polymer and the peptide stacks interact and illustrate the impact of this hydrophobic inner shell approach. This strategy provides a modular approach to fine control the nanotube self-assembling behavior. We expect that this technique will improve the versatility of peptide nanotubes for the engineering of advanced nanomaterials.

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Publication Details

Journal
Angewandte Chemie International Edition
Published
2025-03-31
DOI
https://doi.org/10.1002/anie.202423828
Citations
5
Primary Topic
Supramolecular Self-Assembly in Materials
Type
article
Field-Weighted Citation Impact
2.99
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article

Hydrophobicity‐Controlled Self‐Assembly of Supramolecular Peptide Nanotubes in Water

David K. Chalmers, William H. Parsons, Yixuan Chen, Sébastien Perrier et al.
5 citations
Angewandte Chemie International Edition
Supramolecular Self-Assembly in Materials
2.99
article

Hydrophobicity‐Controlled Self‐Assembly of Supramolecular Peptide Nanotubes in Water

David K. Chalmers, William H. Parsons, Yixuan Chen, Sébastien Perrier, Min Zeng
article en
5 citations

Abstract

Polymer-conjugated peptides are attractive building blocks for the construction of new nanomaterials. However, the ability to control the self-assembly of these materials remains a major limitation to their wider utilization. Herein, we report a facile strategy to fine-tune the assembly of water-soluble hydrophilic polymer-conjugated cyclic peptides by incorporating a defined, short hydrocarbon linker between the polymer and peptide. This addition creates a well-defined hydrophobic "inner shell" that suppresses water from disrupting the organized peptide hydrogen bond network. Our approach is demonstrated using a series of cyclic peptide-linker-PDMA conjugates that were evaluated by asymmetric flow field flow fractionation, small angle neutron scattering and transmission electron microscopy. Molecular dynamics simulations were also used to show how the polymer and the peptide stacks interact and illustrate the impact of this hydrophobic inner shell approach. This strategy provides a modular approach to fine control the nanotube self-assembling behavior. We expect that this technique will improve the versatility of peptide nanotubes for the engineering of advanced nanomaterials.

Angewandte Chemie International EditionVol. 64(22)
University of Warwick (GB), Monash University (AU)
Clean water and sanitation
Openalex Percentile: Top 10%
Supramolecular Self-Assembly in Materials
2.99
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