Guangdong Provincial Key Laboratory of Construction and Detection in Tissue Engineering, Biomaterials Research Center, School of Biomedical Engineering, Southern Medical University, Guangzhou, 510515, PR China.
Key Laboratory of Molecular Target & Clinical Pharmacology and the State Key Laboratory of Respiratory Disease, School of Pharmaceutical Sciences & the Fifth Affiliated Hospital, Guangzhou Medical University, Guangzhou, 511436, PR China.
Biomaterials. 2019 Dec;224:119497. doi: 10.1016/j.biomaterials.2019.119497. Epub 2019 Sep 16.
In recent years, epigenetics has attracted great attentions in the field of biomedicine, which is used to denote the heritable changes in gene expression without any variation in DNA sequence, including DNA methylation, histone modification and so on. Inspired by it, a simple and versatile amino acids modification strategy is proposed in this paper to regulate the subcellular distribution of photosensitizer for plasma membrane targeted photodynamic therapy (PDT). Particularly, the plasma membrane anchoring ability and photo toxicity of the photosensitizer against different cell lines could be effectively manipulated at a single amino acid level. Systematic researches indicate that the number and variety of amino acids have a significant influence on the plasma membrane targeting effect of the photosensitizer. Furthermore, after self-assembling into nanoparticles, the obtained nano photosensitizers (NPs) also exhibit a good biocompatibility and plasma membrane targeting ability, which are conducive to enhancing the PDT therapeutic effect under light irradiation. Both in vitro and in vivo investigations confirm a robust tumor inhibition effect of NPs with a good biocompatibility. This epigenetics-inspired photosensitizer modification strategy would contribute to the development of structure-based drug design for tumor precision therapy.
近年来,表观遗传学在生物医学领域引起了广泛关注,它用于表示基因表达的可遗传变化,而 DNA 序列没有任何变化,包括 DNA 甲基化、组蛋白修饰等。受此启发,本文提出了一种简单通用的氨基酸修饰策略,用于调节用于细胞膜靶向光动力疗法 (PDT) 的光敏剂的亚细胞分布。特别是,可以在单个氨基酸水平上有效操纵光敏剂对不同细胞系的细胞膜锚定能力和光毒性。系统研究表明,氨基酸的数量和种类对光敏剂的细胞膜靶向效果有显著影响。此外,自组装成纳米颗粒后,所得的纳米光敏剂 (NPs) 还表现出良好的生物相容性和细胞膜靶向能力,有利于增强光照射下的 PDT 治疗效果。体外和体内研究均证实了 NPs 具有良好的生物相容性和强大的肿瘤抑制作用。这种受表观遗传学启发的光敏剂修饰策略将有助于基于结构的药物设计用于肿瘤精准治疗。