Ge Ruixin, Chen Miao, Wu Sijin, Huang Sirui, Zhou Ping, Cao Minghui, Zhang Fan, Zang Jinzhi, Zhu Yigao, Li Jingrui, Ni Guilin, Yang Zhihao, Li Qingchao, Pan Wei, Zhang Liang, Liu Min, Xuan Chenghao, Yu Haiyang, Zhou Jun, Xie Songbo
Center for Cell Structure and Function, Collaborative Innovation Center of Cell Biology in Universities of Shandong, College of Life Sciences, Shandong Normal University, Jinan, China.
School of Life Sciences and Medicine, Shandong University of Technology, Zibo, China.
Nat Commun. 2025 May 20;16(1):4683. doi: 10.1038/s41467-025-60039-2.
Oligonucleotide-based medicine faces challenges in efficiently crossing the blood-brain barrier and rapidly reducing toxic proteins. To address these challenges, here we establish an integrated modality, brain-penetrant DNA nanoflowers incorporated with oligonucleotide-based proteolysis targeting chimeras. Using FUS as a proof-of-concept, mutations of which cause frontotemporal dementia and amyotrophic lateral sclerosis, we demonstrate that a FUS-engaging RNA oligonucleotide crosslinked to a ligand for Cereblon efficiently degrade FUS and its cytoplasmic disease-causing mutants through a ubiquitin-proteasomal pathway. The DNA nanoflower contains hundreds of oligonucleotide binding sites and transferrin receptor-engaging aptamers, allowing efficient loading of the oligonucleotide-based degrader and engaging transferrin receptors for brain delivery. A single dose intravenous injection of this modality reaches brain parenchyma within 2 h and degrades 80% FUS protein there, sustained for two weeks without noticeable toxicity. DNA nanoflower oligonucleotide-based degrader is a therapeutic strategy for neurodegenerative diseases that leverages the advantages of designer oligonucleotides and targeted protein degradation.
基于寡核苷酸的药物在有效穿越血脑屏障和快速减少毒性蛋白方面面临挑战。为应对这些挑战,我们在此建立了一种整合模式,即将脑渗透性DNA纳米花与基于寡核苷酸的蛋白酶解靶向嵌合体相结合。以融合蛋白(FUS)作为概念验证,其突变会导致额颞叶痴呆和肌萎缩侧索硬化,我们证明与一种针对 Cereblon 的配体交联的靶向 FUS 的 RNA 寡核苷酸能够通过泛素 - 蛋白酶体途径有效降解 FUS 及其导致细胞质病变的突变体。该 DNA 纳米花包含数百个寡核苷酸结合位点以及与转铁蛋白受体结合的适体,能够高效装载基于寡核苷酸的降解剂,并与转铁蛋白受体结合以实现脑部递送。单次静脉注射这种模式后,在2小时内即可到达脑实质,并在那里降解80%的FUS蛋白,且持续两周无明显毒性。基于DNA纳米花寡核苷酸的降解剂是一种针对神经退行性疾病的治疗策略,它利用了设计寡核苷酸和靶向蛋白降解的优势。