化学
肽
细胞毒性
纳米颗粒
碎片(计算)
劈理(地质)
盐酸阿霉素
组合化学
药物输送
小分子
体外
生物物理学
阿霉素
生物化学
纳米技术
有机化学
岩土工程
计算机科学
化疗
材料科学
断裂(地质)
操作系统
医学
生物
外科
工程类
作者
Tomoya Suma,Jiwei Cui,Markus Müllner,Shiwei Fu,Jenny Tran,Ka Fung Noi,Yi Ju,Frank Caruso
摘要
Peptides perform a diverse range of physiologically important functions. The formulation of nanoparticles directly from functional peptides would therefore offer a versatile and robust platform to produce highly functional therapeutics. Herein, we engineered proapoptotic peptide nanoparticles from mitochondria-disrupting KLAK peptides using a template-assisted approach. The nanoparticles were designed to disassemble into free native peptides via the traceless cleavage of disulfide-based cross-linkers. Furthermore, the cytotoxicity of the nanoparticles was tuned by controlling the kinetics of disulfide bond cleavage, and the rate of regeneration of the native peptide from the precursor species. In addition, a small molecule drug (i.e., doxorubicin hydrochloride) was loaded into the nanoparticles to confer synergistic cytotoxic activity, further highlighting the potential application of KLAK particles in therapeutic delivery.
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