Abstract
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.
Original language | English |
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Pages (from-to) | 9778-9787 |
Number of pages | 10 |
Journal | Nano Letters |
Volume | 23 |
Issue number | 21 |
Early online date | 25 Oct 2023 |
DOIs | |
Publication status | Published - 8 Nov 2023 |
Externally published | Yes |
Bibliographical note
The research is supported by A*STAR (C210112014), Science and Engineering Research Council Central Research Fund (CRF, UIBR, KIMR220901aSERCRF, A*STAR), Health and Biomedical Sciences Industry Alignment Fund Pre-Positioning (IAF-PP) (Grant No. H20C6a0034), and NanoBio Lab (Biomedical Research Council, A*STAR).Keywords
- acid-labile
- agonists and antigen
- cancer therapy
- DNA nanogel
- i-motif