化学
背景(考古学)
肽
范围(计算机科学)
酶
排序酶A
生化工程
分拣酶
组合化学
纳米技术
计算机科学
计算生物学
生物化学
工程类
生物
材料科学
细菌蛋白
古生物学
基因
程序设计语言
作者
Marcel Schmidt,Ana Toplak,Peter J. L. M. Quaedflieg,Jan H. van Maarseveen,Timo Nuijens
标识
DOI:10.1016/j.ddtec.2017.11.007
摘要
The recent advancement of peptide macrocycles as promising therapeutics creates a need for novel methodologies for their efficient synthesis and (large scale) production. Within this context, due to the favorable properties of biocatalysts, enzyme-mediated methodologies have gained great interest. Enzymes such as sortase A, butelase 1, peptiligase and omniligase-1 represent extremely powerful and valuable enzymatic tools for peptide ligation, since they can be applied to generate complex cyclic peptides with exquisite biological activity. Therefore, the use of enzymatic strategies will effectively supplement the scope of existing chemical methodologies and will accelerate the development of future cyclic peptide therapeutics. The advantages and disadvantages of the different enzymatic methodologies will be discussed in this review.
科研通智能强力驱动
Strongly Powered by AbleSci AI