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Engineering unnatural amino acids in peptide linkers enables cathepsin-selective antibody-drug conjugates for HER2-positive breast cancer.

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Engineering unnatural amino acids in peptide linkers enables cathepsin-selective antibody-drug conjugates for HER2-positive breast cancer.

Journal of controlled release : official journal of the Controlled Release Society, 387, 114269

Citation

Gorzeń, Oliwia; Łęcka, Maria; Ćwilichowska-Puślecka, Natalia; Majchrzak, Martyna; Horbach, Natalia; Wiśniewski, Jerzy; Jakimowicz, Piotr; Szpot, Paweł; Zawadzki, Marcin; Dołęga-Kozierowski, Bartosz; Kasprzak, Piotr; Turk, Boris; Drąg, Marcin; Groborz, Katarzyna M; Matkowski, Rafał; Poręba, Marcin. (2025). Engineering unnatural amino acids in peptide linkers enables cathepsin-selective antibody-drug conjugates for HER2-positive breast cancer.. Journal of controlled release : official journal of the Controlled Release Society, 387, 114269. https://doi.org/10.1016/j.jconrel.2025.114269