Co-assembly and self-sorting are not mutually exclusive in enantiomeric peptide systems
4 affiliations
- 1MAX IV Laboratory, Lund University Lund 224 84 Sweden
- 2School of Chemistry, University of Glasgow Glasgow G12 8QQ UK
- 3Department of Biochemistry and Molecular Genetics, University of Virginia Charlottesville VA 22903 USA
- 4ISIS Pulsed Neutron and Muon Source Harwell Science and Innovation Campus Didcot OX11 0QX UK
Abstract
Co-assembly and self-sorting in multicomponent systems are typically treated as mutually exclusive outcomes. Here, we show that this distinction is incomplete. Using enantiomeric peptide nanotubes, we demonstrate that a single co-assembled structure forms only at an equimolar composition, yet remains internally self-sorted into compositionally distinct domains. Contrast-matched neutron scattering directly reveals this segregation and shows that the co-assembled structures adopt layered architectures rather than simple molecular-level mixing. These results establish that co-assembly and self-sorting can coexist within a single supramolecular object across length scales, providing a general framework for understanding and controlling multicomponent self-assembly.
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BibTeX
@article{bianco2026coassembly,
title = {{Co-assembly and self-sorting are not mutually exclusive in enantiomeric peptide systems}},
author = {Simona Bianco and Ravi R. Sonani and Libby J. Marshall and Alex S. Loch and James Doutch and Edward H. Egelman and Dave J. Adams},
journal = {Chemical Science},
year = {2026},
month = aug,
doi = {10.1039/d6sc04454a},
url = {https://doi.org/10.1039/d6sc04454a},
note = {CC BY 3.0},
}
RIS
TY - JOUR
TI - Co-assembly and self-sorting are not mutually exclusive in enantiomeric peptide systems
AU - Simona Bianco
AU - Ravi R. Sonani
AU - Libby J. Marshall
AU - Alex S. Loch
AU - James Doutch
AU - Edward H. Egelman
AU - Dave J. Adams
PY - 2026
DA - 2026/08/27
JO - Chemical Science
DO - 10.1039/d6sc04454a
UR - https://doi.org/10.1039/d6sc04454a
AB - Co-assembly and self-sorting in multicomponent systems are typically treated as mutually exclusive outcomes. Here, we show that this distinction is incomplete. Using enantiomeric peptide nanotubes, we demonstrate that a single co-assembled structure forms only at an equimolar composition, yet remains internally self-sorted into compositionally distinct domains. Contrast-matched neutron scattering directly reveals this segregation and shows that the co-assembled structures adopt layered architectures rather than simple molecular-level mixing. These results establish that co-assembly and self-sorting can coexist within a single supramolecular object across length scales, providing a general framework for understanding and controlling multicomponent self-assembly.
SN - 2041-6520
SN - 2041-6539
ER -