肽
背景(考古学)
酶
计算生物学
组合化学
代谢稳定性
生物合成
化学
生物化学
计算机科学
生物
体外
古生物学
标识
DOI:10.1016/j.biotechadv.2022.107908
摘要
The increasing length and complexity of peptide drug candidates foster the development of novel strategies for their manufacture, which should include sustainable and efficient technologies. In this context, including enzymatic catalysis in the production of peptide molecules has gained interest. Here, several enzymes from ribosomally synthesized and post-translationally modified peptides biosynthesis pathways are reviewed, with attention to their capacity to introduce stability-promoting structural features on peptides, providing an initial framework towards their use in therapeutic peptide production processes.
科研通智能强力驱动
Strongly Powered by AbleSci AI