化学
肽
血脑屏障
渗透(战争)
生物物理学
寡肽
离体
细胞穿透肽
体内
薄壁组织
半胱氨酸
生物化学
体外
神经科学
中枢神经系统
酶
病理
医学
生物
工程类
生物技术
运筹学
作者
Colin M. Fadzen,Justin M. Wolfe,Choi‐Fong Cho,E. Antonio Chiocca,Sean E. Lawler,Bradley L. Pentelute
摘要
Here we describe the utility of peptide macrocyclization through perfluoroaryl-cysteine SNAr chemistry to improve the ability of peptides to cross the blood–brain barrier. Multiple macrocyclic analogues of the peptide transportan-10 were investigated that displayed increased uptake in two different cell lines and improved proteolytic stability. One of these analogues (M13) exhibited substantially increased delivery across a cellular spheroid model of the blood–brain barrier. Through ex vivo imaging of mouse brains, we demonstrated that this perfluoroarene-based macrocycle of TP10 exhibits increased penetration of the brain parenchyma following intravenous administration in mice. Finally, we evaluated macrocyclic analogues of the BH3 domain of the BIM protein to assess if our approach would be applicable to a peptide of therapeutic interest. We identified a BIM BH3 analogue that showed increased penetration of the brain tissue in mice.
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