7BZA

Template lasso peptide C24

7BZA の概要

• エントリーDOI: 10.2210/pdb7bza/pdb
• NMR情報: BMRB: 36351
• 分子名称: lasso peptide (1 entity in total)
• 機能のキーワード: heterologous expression, site-direct mutagenesis, antibiotic
• 由来する生物種: Streptomyces sp.
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 1714.96

構造登録者

Liu, X.H.,Liu, T.,Ma, X.J.,Yu, J.H.,Yang, D.H.,Ma, M. (登録日: 2020-04-27, 公開日: 2021-04-28, 最終更新日: 2024-05-15)

主引用文献

Liu, T.,Ma, X.,Yu, J.,Yang, W.,Wang, G.,Wang, Z.,Ge, Y.,Song, J.,Han, H.,Zhang, W.,Yang, D.,Liu, X.,Ma, M.
Rational generation of lasso peptides based on biosynthetic gene mutations and site-selective chemical modifications.
Chem Sci, 12:12353-12364, 2021

PubMed Abstract: Lasso peptides are a unique family of natural products whose structures feature a specific threaded fold, which confers these peptides the resistance to thermal and proteolytic degradation. This stability gives lasso peptides excellent pharmacokinetic properties, which together with their diverse reported bioactivities have garnered extensive attention because of their drug development potential. Notably, the threaded fold has proven quite inaccessible by chemical synthesis, which has hindered efficient generation of structurally diverse lasso peptides. We herein report the discovery of a new lasso peptide stlassin () by gene activation based on a heterologous expression system. Site-directed mutagenesis on the precursor peptide-encoding gene is carried out systematically, generating 17 stlassin derivatives ( and ) with residue-replacements at specific positions of . The solution NMR structures of , , , and are determined, supporting structural comparisons that ultimately enabled the rational production of disulfide bond-containing derivatives and , whose structures do not belong to any of the four classes currently used to classify lasso peptides. Several site-selective chemical modifications are first applied on and , efficiently generating new derivatives (, ) whose structures bear various decorations beyond the peptidyl monotonicity. The high production yields of these stlassin derivatives facilitate biological assays, which show that , , , , and possess antagonistic activities against the binding of lipopolysaccharides to toll-like receptor 4 (TLR4). These results demonstrate proof-of-concept for the combined mutational/chemical generation of lasso peptide libraries to support drug lead development.

PubMed: 34603665
DOI: 10.1039/d1sc02695j

実験手法

SOLUTION NMR