结合
有效载荷(计算)
药物输送
化学
共轭体系
DNA
组合化学
纳米技术
计算生物学
连锁反应
靶向给药
模块化设计
寡核苷酸
药品
基因传递
计算机科学
生物物理学
生物标志物
费斯特共振能量转移
荧光
前药
毒品携带者
分子探针
输送系统
DNA纳米技术
作者
Sikai Chen,Miguel López-Tena,Francesco Russo,Emma E. Watson,Millicent Dockerill,Javier Cabello García,Sofía Barluenga,Nicolas Winssinger
标识
DOI:10.1038/s41587-026-03044-0
摘要
Antibody-drug conjugates enable highly specific delivery of potent cytotoxics to biomarker-expressing cells. In parallel, advances in DNA circuitry and DNA-protein conjugates have allowed programmable integration of molecular inputs and signal amplification via hybridization chain reactions (HCRs). Here we present a system using affibody-DNA and aptamer-DNA conjugates to execute a Boolean logic operation on cell-surface biomarkers, resulting in amplified payload delivery using an HCR of DNA-drug conjugates. Proximity-induced assembly of the biomarker binders generates the initiator that triggers an HCR. The resulting assembly undergoes endocytosis, enabling controlled payload release of drugs conjugated to the DNA with cathepsin-cleavable linkers. We show that DNA-drug conjugates achieve targeted delivery with >100-fold amplification relative to the input biomarkers using fluorescence quantifications. We also identify payloads that strongly influence delivery efficiency and demonstrate delivery of different drug combinations. Finally, we show that biomarker-triggered HCRs can recruit generic antibodies. This modular technology enables tailored combinations of biomarker inputs and drug outputs toward more precise and personalized treatment.
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