Abstract
HER2-expressing cancers currently benefit from targeted therapies, including monoclonal antibodies and antibody-drug conjugates that specifically bind to the extracellular domain of the receptor. Peptides targeting HER2 represent promising candidates for the development of alternative molecular drugs. In this study, we report a dimeric version of the previously validated A9 peptide as a ligand specifically targeting HER2. The novel A9-PEG-A9 conjugate consists of two A9 peptides whose N-terminal amino groups are linked via a polyethylene glycol chain. It was synthesized using a solvent-free protocol and validated as an improved ligand, demonstrating enhanced water solubility and increased affinity for the model receptor HER2-DIVMP, as determined by the fluorescence spectroscopy titration method.
| Lingua originale | Inglese |
|---|---|
| pagine (da-a) | 16299-16305 |
| Numero di pagine | 7 |
| Rivista | Journal of Medicinal Chemistry |
| Volume | 68 |
| Numero di pubblicazione | 15 |
| DOI | |
| Stato di pubblicazione | Pubblicato - 14 ago 2025 |
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