寡核苷酸
计算生物学
体内
模块化设计
向性
体外
生物
结合
合理设计
输送系统
计算机科学
纳米技术
化学
细胞生物学
临床前试验
生物信息学
DNA
双绞线
作者
Xucheng Hou,Changyue Yu,Yonger Xue,Yuwei Liu,Diana D. Kang,Jeffrey Bennett,Eliza Bliss‐Moreau,Mi Ni,Yujie Liu,Gang Fang,Ya Ying Zheng,Siyu Wang,Meng Tian,Yichen Zhong,Haoyuan Li,Zhengwei Liu,Dinglingge Cao,Yizhou Dong
标识
DOI:10.1016/j.bioactmat.2026.08.058
摘要
The therapeutic potential of oligonucleotides (oligos) is limited by insufficient delivery to extrahepatic tissues. In vitro assays often fail to accurately predict in vivo behavior, while testing each oligo candidate in animals remains inherently low throughput. Here, we conceive a barcoded oligonucleotide system (BOLT), a platform that enables high-throughput in vivo evaluations of small-molecule ligands and identifies tissue-specific oligo delivery. BOLT integrates rational design of oligo barcodes, modular conjugation chemistry, and next-generation sequencing (NGS)-based quantification, allowing simultaneous evaluation of many chemically diverse ligand-oligo conjugates within a single animal. Notably, this platform is applicable in both mice and nonhuman primates (NHPs). Using BOLT, we discovered ligands with tropism for tissues such as the brain, lung, and muscle. Collectively, these results indicate that the BOLT platform can accelerate the discovery of tissue-targeting ligands for broad oligo therapeutics.
科研通智能强力驱动
Strongly Powered by AbleSci AI