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工程化E2生物纳米颗粒用于将化疗药物靶向递送至乳腺癌细胞

Engineering E2 Bionanoparticles for Targeted Delivery of Chemotherapeutics to Breast Cancer Cells.

作者信息

Sullivan Millicent O, Chen Wilfred

机构信息

Department of Chemical and Biomolecular Engineering, University of Delaware, Newark, DE, USA.

出版信息

Methods Mol Biol. 2024;2720:177-189. doi: 10.1007/978-1-0716-3469-1_13.

Abstract

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.

摘要

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。

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