Elashal Hader E, Raj Monika
Department of Chemistry, Seton Hall University, 400 South Orange Ave, South Orange, NJ 07079, USA.
Chem Commun (Camb). 2016 May 7;52(37):6304-7. doi: 10.1039/c6cc01509c. Epub 2016 Apr 18.
Site-selective cleavage of extremely unreactive peptide bonds is a very important chemical modification that provides invaluable information regarding protein sequence, and it acts as a modulator of protein structure and function for therapeutic applications. For controlled and selective cleavage, a daunting task, chemical reagents must selectively recognize or bind to one or more amino acid residues in the peptide chain and selectively cleave a peptide bond. Building on this principle, we have developed an approach that utilizes a chemical reagent to selectively modify the serine residue in a peptide chain and leads to the cleavage of a peptide backbone at the N-terminus of the serine residue. After cleavage, modified residues can be converted back to the original fragments. This method exhibits broad substrate scope and selectively cleaves various bioactive peptides with post-translational modifications (e.g. N-acetylation and -methylation) and mutations (d- and β-amino acids), which are a known cause of age related diseases.
对极难反应的肽键进行位点选择性切割是一种非常重要的化学修饰,它能提供有关蛋白质序列的宝贵信息,并且在治疗应用中作为蛋白质结构和功能的调节剂。对于这种可控且选择性的切割这一艰巨任务,化学试剂必须选择性地识别或结合肽链中的一个或多个氨基酸残基,并选择性地切割肽键。基于这一原理,我们开发了一种方法,利用化学试剂选择性地修饰肽链中的丝氨酸残基,并导致在丝氨酸残基的N端切割肽主链。切割后,修饰的残基可以转化回原始片段。该方法具有广泛的底物范围,能选择性地切割各种具有翻译后修饰(如N-乙酰化和N-甲基化)以及突变(D-和β-氨基酸)的生物活性肽,而这些修饰和突变是与年龄相关疾病的已知病因。