化学
四肽
组织蛋白酶
组织蛋白酶
生物化学
组织蛋白酶E
组织蛋白酶H
组织蛋白酶O
组织蛋白酶L
肽
氨基酸
组织蛋白酶D
组织蛋白酶B
肽库
组织蛋白酶C
结合
癌细胞
寡肽
半胱氨酸
组织蛋白酶A
分子生物学
细胞毒性
天然化学连接
肽合成
化学生物学
蛋白质工程
组织蛋白酶L1
作者
Maria Łęcka,Oliwia Gorzeń,Natalia Ćwilichowska-Puślecka,Julia Nguyen,Martyna Majchrzak,Vanessa Pippa,Piotr Jakimowicz,Jerzy Wiśniewski,Bartosz Dołęga-Kozierowski,Piotr Kasprzak,Boris Turk,Marcin Drąg,Rafal Matkowski,Marcin Poręba
标识
DOI:10.1021/acs.jmedchem.6c00202
摘要
Cysteine cathepsins, particularly cathepsin S, regulate proteolytic signaling in cancer progression and immune modulation, yet selective tools for individual cathepsins remain limited. Here, we report the design of cathepsin S-selective probes and cathepsin S-cleavable antibody-drug conjugates (ADCs) using substrate profiling with unnatural amino acids. Hybrid Combinatorial Substrate Library (HyCoSuL) screening identified selective tetrapeptide motifs that were used to develop optimized fluorogenic substrates, irreversible inhibitors, and fluorescent activity-based probes with high selectivity for cathepsin S in biochemical and cellular assays. These peptide motifs were then incorporated as cleavable linkers in MMAE-based ADCs targeting HER-2 or TROP-2, enabling cathepsin S-dependent cytotoxicity across breast cancer models with distinct target-expression profiles. Finally, anti-cathepsin S antibodies combined with CyTOF analysis revealed the spatial distribution of cathepsin S and its coexpression with HER-2 and TROP-2 in breast cancer patient samples, suggesting that cathepsin S profiling may help inform future patient stratification strategies for cathepsin S-activated ADC therapy.
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