7YAA

Crystal structure analysis of cp3 bound BCLxl

7YAA の概要

• エントリーDOI: 10.2210/pdb7yaa/pdb
• 分子名称: Bcl-2-like protein 1, cp3 peptide, GLYCEROL, ... (5 entities in total)
• 機能のキーワード: complex, apoptosis
• 由来する生物種: Homo sapiens (human); 詳細
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 17878.01

構造登録者

Li, F.W.,Liu, C.,Wu, C.L.,Wu, D.L. (登録日: 2022-06-27, 公開日: 2023-11-15, 最終更新日: 2024-10-16)

主引用文献

Li, F.,Liu, J.,Liu, C.,Liu, Z.,Peng, X.,Huang, Y.,Chen, X.,Sun, X.,Wang, S.,Chen, W.,Xiong, D.,Diao, X.,Wang, S.,Zhuang, J.,Wu, C.,Wu, D.
Cyclic peptides discriminate BCL-2 and its clinical mutants from BCL-X L by engaging a single-residue discrepancy.
Nat Commun, 15:1476-1476, 2024

PubMed Abstract: Overexpressed pro-survival B-cell lymphoma-2 (BCL-2) family proteins BCL-2 and BCL-X can render tumor cells malignant. Leukemia drug venetoclax is currently the only approved selective BCL-2 inhibitor. However, its application has led to an emergence of resistant mutations, calling for drugs with an innovative mechanism of action. Herein we present cyclic peptides (CPs) with nanomolar-level binding affinities to BCL-2 or BCL-X, and further reveal the structural and functional mechanisms of how these CPs target two proteins in a fashion that is remarkably different from traditional small-molecule inhibitors. In addition, these CPs can bind to the venetoclax-resistant clinical BCL-2 mutants with similar affinities as to the wild-type protein. Furthermore, we identify a single-residue discrepancy between BCL-2 D111 and BCL-X A104 as a molecular "switch" that can differently engage CPs. Our study suggests that CPs may inhibit BCL-2 or BCL-X by delicately modulating protein-protein interactions, potentially benefiting the development of next-generation therapeutics.

PubMed: 38368459
DOI: 10.1038/s41467-024-45848-1

実験手法

X-RAY DIFFRACTION (1.4 Å)