Abstract
Chemokines are secreted blood proteins that steer leukocyte migration in the inflammatory response. Neutralization of chemokines is believed to be a beneficial therapeutic strategy for the treatment of inflammation-associated diseases. Proteolytically stable chemokine-binding peptides could be suitable candidates for the development of chemokine-neutralizing agents. Here, we report the mirror-image phage display selection of cyclic all-D-peptides against the C-X-C motif chemokine ligand 8 (CXCL8). Selection yielded structurally diverse all-D-peptides with submicromolar affinity to the target CXCL8 chemokine and different selectivity to related chemokines. Binding of these all-D-peptides caused dissociation of the native CXCL8 dimer and disruption of its binding to GAGs, without an effect on in vitro cell migration. This work demonstrates the example of mirror-image phage display selection of cyclized all-D-peptides and its utility for the development of chemokine-binding agents.
| Original language | English |
|---|---|
| Pages (from-to) | 2798-2807 |
| Number of pages | 10 |
| Journal | ACS Chemical Biology |
| Volume | 20 |
| Issue number | 11 |
| DOIs | |
| Publication status | Published - 1 Oct 2025 |
Keywords
- SECONDARY STRUCTURE
- CXCL8
- MIMICRY
- TARGET
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