化学
肽
组合化学
计算生物学
生物催化
纳米技术
生物化学
前蛋白转化酶
蓝图
酶
环肽
可扩展性
结合亲和力
生物相容性材料
仿生材料
肽合成
作者
Artis Klapars,Anna Fryszkowska,Stephanie Galanie,Omer Ad,Ellen Y. Aguilera,Nnamdi Akporji,Chihui An,Stephanus Axnanda,Tewoderos M. Ayele,Richard Ayikpoe,Rodell C. Barrientos,Matthew R. Bauerle,M. Becker,Kevin M. Belyk,Lisa Bereznitski,Jackson K. B. Cahn,Karla Camacho Soto,Louis‐Charles Campeau,Kevin R. Campos,Anagha Chandra
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2026-05-07
卷期号:392 (6798): 643-647
标识
DOI:10.1126/science.aed8713
摘要
Historically, many compelling therapeutic targets have been accessible only by injectable biologic drugs. Macrocyclic peptides, such as the proprotein convertase subtilisin/kexin type 9 inhibitor enlicitide for the treatment of atherosclerotic cardiovascular disease, are beginning to unlock these targets to orally administered therapies to enable broader patient access. We report the convergent biocatalytic assembly of enlicitide from simple building blocks enabled by a suite of engineered enzymes to catalyze selective peptide fragment formation, coupling, and macrocyclization in a protecting group-free manner. Together with efficient crystallizations that obviate the need for chromatography, this approach reduces the number of steps by greater than half compared with prior state-of-the-art methods, addressing long-standing synthetic challenges and offering a sustainable blueprint for the scalable development of complex peptide therapeutics.
科研通智能强力驱动
Strongly Powered by AbleSci AI