Institute of Materials Research and Engineering (IMRE), Agency for Science, Technology and Research (A*STAR), 2 Fusionopolis Way, Innovis #08-03, Singapore 138634, Republic of Singapore.
NanoBio Lab, Agency for Science, Technology and Research (A*STAR), 31 Biopolis Way, The Nanos, #09-01, Singapore 138669, Republic of Singapore.
Nano Lett. 2023 Nov 8;23(21):9778-9787. doi: 10.1021/acs.nanolett.3c02449. Epub 2023 Oct 25.
The development of precisely engineered vehicles for intracellular delivery and the controlled release of payloads remains a challenge. DNA-based nanomaterials offer a promising solution based on the A-T-G-C alphabet-dictated predictable assembly and high programmability. Herein, we present a self-immolative DNA nanogel vaccine, which can be tracelessly released in the intracellular compartments and activate the immune response. Three building blocks with cytosine-rich overhang domains are designed to self-assemble into a DNA nanogel framework with a controlled size. Two oligo agonists and one antigen peptide are conjugated to the building blocks via an acid-labile chemical linker. Upon internalization into acidic endosomes, the formation of i-motif configurations leads to dissociation of the DNA nanogel vaccine. The acid-labile chemical linker is cleaved, releasing the agonists and antigen in their traceless original form to activate antigen-presenting cells and an immune response. This study presents a novel strategy for constructing delivery platforms for intracellularly stimuli-triggered traceless release of therapeutics.
精确工程化的细胞内递药载体和载药可控释放的发展仍然是一个挑战。基于 DNA 的纳米材料提供了一种有前途的解决方案,基于 A-T-G-C 字母指令的可预测组装和高可编程性。在此,我们提出了一种自毁性 DNA 纳米凝胶疫苗,它可以在细胞内室中无痕迹释放并激活免疫反应。三个带有胞嘧啶丰富突出结构域的构建块被设计成自组装成具有可控尺寸的 DNA 纳米凝胶框架。两个寡核苷酸激动剂和一个抗原肽通过酸不稳定的化学连接子连接到构建块上。进入酸性内涵体后,i- 发夹结构的形成导致 DNA 纳米凝胶疫苗的解离。酸不稳定的化学连接子被切割,释放出激动剂和抗原的无痕迹原始形式,以激活抗原呈递细胞和免疫反应。这项研究提出了一种构建用于细胞内刺激触发无痕迹释放治疗剂的递药平台的新策略。