蛋白酵素
化学
肽
生物正交化学
生物化学
蛋白酶
半胱氨酸
肽序列
靶肽
计算生物学
重组DNA
酶
序列(生物学)
组合化学
蛋白质标签
翻译后修饰
蛋白质测序
限制
氨基酸
肽合成
天然化学连接
蛋白质工程
劈开
作者
Yukun Zhou,Guangzhao Xiao,Sicong Yao,YuQian Zhang,Yang Yongqin,Qinghui Yang,Xiaoman Liu,Yanmei Wang,Yapei Wu,Yang Liu,Yu‐Hsuan Tsai,Yiwu Zheng
摘要
Abstract Proteases responsible for leader peptide removal are ubiquitous in ribosomally synthesized and post-translationally modified peptide (RiPP) biosynthetic pathways. However, many characterized RiPP proteases require specific core peptide modifications prior to cleavage, limiting their broader applicability. Here, we identified a cyanobactin protease clade that efficiently processes diverse peptide substrates while maintaining strict recognition-sequence selectivity. We demonstrated that GusA, a representative member of this clade, can be used for the processing of structurally complex modified peptides and the removal of affinity tags from recombinant proteins. GusA-mediated exposure of N-terminal cysteine residues can also be applied to the construction of chemically diversified asymmetric phage-displayed macrocyclic peptide libraries, from which nanomolar-affinity ligands against Keap1 and Bcl-xL were identified, providing valuable tools for biological studies and potential therapeutics. The same strategy was further applied to site-selective and multicolor labeling of mammalian cell-surface proteins, demonstrating that GusA-mediated N-terminal cysteine generation can be readily integrated with bioorthogonal labeling chemistries. Together, our results establish cyanobactin proteases as an underexplored source of sequence-selective biocatalysts for site-selective peptide and protein modification.
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