Shi Yan, Sang Peng, Yin Guangqiang, Gao Ruixuan, Liang Xiao, Brzozowski Robert, Odom Timothy, Eswara Prahathees, Zheng Youxuan, Li Xiaopeng, Cai Jianfeng
Department of Chemistry, University of South Florida, 4202 East Fowler Avenue, Tampa, Florida 33620, United States.
State Key Laboratory of Coordination Chemistry, School of Chemistry and Chemical Engineering, Nanjing University, 210023 Nanjing, China.
Adv Opt Mater. 2020 Jul 20;8(14). doi: 10.1002/adom.201902122. Epub 2020 Apr 20.
Through our continuous effort in developing a new class of foldamers, we have both designed and synthesized homogenous sulfono-γ-AApeptides using tetraphenylethylene (TPE) moieties attached to the backbone as luminogenic sidechains. Based on previous crystal structures, we have found that these foldamers adopted a left-handed 4-helix. Due to the constraint of the helical scaffold, the rotation of the TPE moieties were restricted, leading to fluorescent emissive properties with high quantum yields not only at the aggregate state but also in solution. Investigation of the relationship between the structure and fluorescence behavior reveals that emission was induced by the combined effect of the aggregation-induced emission (AIE) and the rotated restriction from the backbone. Furthermore, as the packing mode of the luminogens could be precisely adjusted by the helical backbone, these foldamers were found to be circularly polarizable with relatively large luminescence dissymmetry factor ( ). Interestingly, possessing cationic amphipathic structures similar to that of host-defense peptides (HDPs), these sulfono-γ-AApeptides were able to inhibit the growth of Gram-positive bacteria methicillin-resistant (MRSA) through membrane interactions.
通过我们在开发新型折叠体方面的持续努力,我们设计并合成了均一的磺酰基-γ-氨基酸肽,其使用连接在主链上的四苯乙烯(TPE)部分作为发光侧链。基于先前的晶体结构,我们发现这些折叠体呈现左手4螺旋结构。由于螺旋支架的限制,TPE部分的旋转受到限制,不仅在聚集态而且在溶液中都导致具有高量子产率的荧光发射特性。对结构与荧光行为之间关系的研究表明,发射是由聚集诱导发光(AIE)和主链旋转限制的综合作用引起的。此外,由于发光团的堆积模式可以通过螺旋主链精确调节,发现这些折叠体具有相对较大的发光不对称因子( ),可实现圆偏振。有趣的是,这些磺酰基-γ-氨基酸肽具有与宿主防御肽(HDPs)相似的阳离子两亲结构,能够通过膜相互作用抑制革兰氏阳性耐甲氧西林金黄色葡萄球菌(MRSA)的生长。