Opportunities and challenges of RiPP-based therapeutics

被引:4
|
作者
Pfeiffer, Isabel P. -M. [1 ]
Schroeder, Maria-Paula [1 ]
Mordhorst, Silja [1 ]
机构
[1] Univ Tubingen, Pharmaceut Inst, Dept Pharmaceut Biol, Morgenstelle 8, D-72076 Tubingen, Germany
关键词
NATRIURETIC-FACTOR ANF; B RECEPTOR ANTAGONIST; CYSTINE-KNOT PEPTIDES; HALF-LIFE EXTENSION; IN-VITRO; NATURAL-PRODUCTS; LASSO PEPTIDE; STREPTOMYCES SP; LEADER PEPTIDE; PLASMODIUM-GALLINACEUM;
D O I
10.1039/d3np00057e
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Covering: up to 2024Ribosomally synthesised and post-translationally modified peptides (RiPPs) comprise a substantial group of peptide natural products exhibiting noteworthy bioactivities ranging from antiinfective to anticancer and analgesic effects. Furthermore, RiPP biosynthetic pathways represent promising production routes for complex peptide drugs, and the RiPP technology is well-suited for peptide engineering to produce derivatives with specific functions. Thus, RiPP natural products possess features that render them potentially ideal candidates for drug discovery and development. Nonetheless, only a small number of RiPP-derived compounds have successfully reached the market thus far. This review initially outlines the therapeutic opportunities that RiPP-based compounds can offer, whilst subsequently discussing the limitations that require resolution in order to fully exploit the potential of RiPPs towards the development of innovative drugs. Ribosomally synthesised and post-translationally modified peptides (RiPPs) are highly promising candidates for drug discovery and development, but challenges remain.
引用
收藏
页码:990 / 1019
页数:30
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