ARC Centre of Excellence in Convergent Bio-Nano Science and Technology, and the Department of Chemical and Biomolecular Engineering, The University of Melbourne , Parkville, Victoria 3010, Australia.
Key Centre for Polymers and Colloids, School of Chemistry, The University of Sydney , Sydney, NSW 2006, Australia.
J Am Chem Soc. 2017 Mar 22;139(11):4009-4018. doi: 10.1021/jacs.6b11302. Epub 2017 Mar 13.
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.
肽具有多种重要的生理功能。因此,直接从功能肽中构建纳米粒子将为生产高度功能化的治疗药物提供一个通用且强大的平台。在这里,我们使用模板辅助的方法从破坏线粒体的 KLAK 肽中设计了促凋亡肽纳米颗粒。这些纳米颗粒被设计成通过无痕迹的二硫键交联剂裂解分解成游离的天然肽。此外,通过控制二硫键裂解的动力学以及前体物质中原肽的再生速率,可以调节纳米颗粒的细胞毒性。此外,将小分子药物(即盐酸多柔比星)载入纳米颗粒中以赋予协同细胞毒性活性,进一步突出了 KLAK 颗粒在治疗药物输送中的应用潜力。