DNA
肽
生物
HMG盒
生物化学
DNA结合蛋白
计算生物学
结合位点
结合选择性
蛋白质-DNA相互作用
化学
转录因子
基因
作者
André R. Paquette,Christopher N. Boddy
出处
期刊:ChemBioChem
[Wiley]
日期:2023-09-26
卷期号:24 (24)
被引量:5
标识
DOI:10.1002/cbic.202300594
摘要
Stapled peptides have rapidly established themselves as a powerful technique to mimic α-helical interactions with a short peptide sequence. There are many examples of stapled peptides that successfully disrupt α-helix-mediated protein-protein interactions, with an example currently in clinical trials. DNA-protein interactions are also often mediated by α-helices and are involved in all transcriptional regulation processes. Unlike DNA-binding small molecules, which typically lack DNA sequence selectivity, DNA-binding proteins bind with high affinity and high selectivity. These are ideal candidates for the design DNA-binding stapled peptides. Despite the parallel to protein-protein interaction disrupting stapled peptides and the need for sequence specific DNA binders, there are very few DNA-binding stapled peptides. In this review we examine all the known DNA-binding stapled peptides. Their design concepts are compared to stapled peptides that disrupt protein-protein interactions and based on the few examples in the literature, DNA-binding stapled peptide trends are discussed.
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