化学
反平行(数学)
超分子化学
三聚体
抗菌剂
位阻效应
肽
立体化学
抗菌肽
拉链
晶体结构
结晶学
生物物理学
生物化学
有机化学
二聚体
物理
磁场
生物
量子力学
计算机科学
算法
作者
Conan K. Wang,Gordon J. King,Anne C. Conibear,Mariana C. Ramos,Stephanie Chaousis,Sónia Troeira Henriques,David J. Craik
摘要
Enantiomeric forms of BTD-2, PG-1, and PM-1 were synthesized to delineate the structure and function of these β-sheet antimicrobial peptides. Activity and lipid-binding assays confirm that these peptides act via a receptor-independent mechanism involving membrane interaction. The racemic crystal structure of BTD-2 solved at 1.45 Å revealed a novel oligomeric form of β-sheet antimicrobial peptides within the unit cell: an antiparallel trimer, which we suggest might be related to its membrane-active form. The BTD-2 oligomer extends into a larger supramolecular state that spans the crystal lattice, featuring a steric-zipper motif that is common in structures of amyloid-forming peptides. The supramolecular structure of BTD-2 thus represents a new mode of fibril-like assembly not previously observed for antimicrobial peptides, providing structural evidence linking antimicrobial and amyloid peptides.
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