Sullivan Millicent O, Chen Wilfred
Department of Chemical and Biomolecular Engineering, University of Delaware, Newark, DE, USA.
Methods Mol Biol. 2024;2720:177-189. doi: 10.1007/978-1-0716-3469-1_13.
Naturally occurring protein nanocages are promising drug carriers as both the interior and exterior can be decorated for drug encapsulation and cell targeting. To provide surface functionalization, we added a SpyTag to E2 nanocages (ST-E2) to enable tunable decoration using the robust SpyCatcher bioconjugation strategy. Additionally, the E2 core was mutated with four phenylalanine substitutions for doxorubicin loading and pH-responsive release. By decorating the exterior with a highly cell-specific epidermal growth factor receptor (EGFR)-targeting protein conjugate, 4GE11-mCherry-SpyCatcher, we demonstrated targeted cell death in inflammatory breast cancer cells compared to healthy breast epithelial cells at concentrations below the IC50 of free doxorubicin.
天然存在的蛋白质纳米笼是很有前景的药物载体,因为其内部和外部都可以进行修饰以用于药物封装和细胞靶向。为了实现表面功能化,我们在E2纳米笼(ST-E2)上添加了一个SpyTag,以便使用强大的SpyCatcher生物共轭策略进行可调谐修饰。此外,对E2核心进行了四个苯丙氨酸取代的突变,用于阿霉素负载和pH响应释放。通过用高度细胞特异性的表皮生长因子受体(EGFR)靶向蛋白共轭物4GE11-mCherry-SpyCatcher修饰外部,我们证明了在低于游离阿霉素IC50的浓度下,与健康乳腺上皮细胞相比,炎性乳腺癌细胞中存在靶向细胞死亡。