Castelletto, V., de Mello, L. R., Seitsonen, J. and Hamley, I. W.
ORCID: https://orcid.org/0000-0002-4549-0926
(2026)
Fibrillar and Micellar Aggregation of Semaglutide and Formation of a Chiral-Imprinted Glass.
Biomacromolecules, 27 (4).
ISSN 1525-7797
doi: 10.1021/acs.biomac.5c02669
Abstract/Summary
Semaglutide is a therapeutically important lipopeptide that comprises a lipidated peptide with a glucagon-like peptide-1 (GLP-1) sequence, and may be prone to aggregation. We show that semaglutide in low pH 2.4 solutions forms β-sheet fibrils, in contrast to the oligomeric and micellar structures formed at higher pH. Based on cryo-TEM images showing twisted fibrils and the modeling of SAXS data (and with knowledge from fiber XRD) and molecular dynamics simulations, a model for the β-sheet structure is proposed, which comprises curved β-strands arranged in an antiparallel fashion around a core that comprises the lipidated lysine residue. This structure results from the patterning of the charged, polar, hydrophobic, and lipidated residues. Remarkably, it is possible to form a glass from the base form of semaglutide with crotonic acid, an organic salt capable of hydrogen bonding. Semaglutide glasses may have applications in biomedicine or therapeutics (for example, as slow-release depots).
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| Item Type | Article |
| URI | https://reading-pure-test.eprints-hosting.org/id/eprint/128501 |
| Identification Number/DOI | 10.1021/acs.biomac.5c02669 |
| Refereed | Yes |
| Divisions | Life Sciences > School of Chemistry, Food and Pharmacy > Department of Chemistry |
| Download/View statistics | View download statistics for this item |
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