化学
肽
转录因子
细胞内
分子生物学
抄写(语言学)
细胞培养
生物
细胞生物学
体外
生物化学
生物活性
转染
作用机理
药理学
作者
Andrew Brennan,Keith W. Vance,Jody M. Mason
标识
DOI:10.1016/j.chembiol.2026.02.002
摘要
Transcription factors remain essential yet intractable targets for drug discovery owing to their flat, dynamic interfaces. We present an intracellular cyclization strategy that enables in-cell generation of conformationally constrained peptide libraries. Bis-alkylating reagents traverse bacterial membranes and selectively bridge cysteine pairs, permitting post-translational peptide stapling during in vivo screening. Integrated with the transcription block survival (TBS) assay, this intracellular-cyclization TBS (icTBS) platform simultaneously selects both peptide sequence and optimal constraint site, eliminating iterative synthesis. Libraries directed against the oncogenic transcription factor CREB1 yielded three nanomolar-affinity antagonists, with cyclized variants selected by icTBS displaying enhanced functional activity in cellular assays. The lead peptide penetrated melanoma and colorectal cancer cells, suppressed CREB1-dependent transcription, reduced oncogenic protein expression, and triggered apoptosis. icTBS thus provides a general, genetically encoded route to discover constrained peptide therapeutics that disrupt protein-DNA interfaces previously considered "undruggable."
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