DNAPC4ImunoMol · DNA modules as communicators in tumor immunomodulation
Horizon Europe — Marie Skłodowska-Curie Actions
- Duration
- 2023-05-01 → 2025-04-30
- EU contribution
- €173,847
- Participants
- 2
- Scheme
- HORIZON-TMA-MSCA-PF-EF
Lines connect the coordinator with its partners.
Results in brief
DNA modules as communicators in tumor immunomodulation
Certain diseases present themselves as a complex molecular scenario. In these diseases, of which the most important examples are cancer and autoimmune diseases, a single treatment, e.g. a drug, only works under strict conditions. Therefore, the disease must be characterized by so-called markers. These can be small molecules, proteins or other features that represent the biochemical state of the disease. Today, complex diseases are treated by diagnosing the disease, characterizing the conditions and then applying appropriate treatments. In the future, these three steps will be performed simultaneously by molecular computers. Molecular computers are sets of molecules that are designed to interact with each other and with target molecules so that they can be used to determine whether a molecule is present or not (e.g. a cancer marker) and then trigger a further response, the treatment, but only if the right markers are present. In other words, the diagnosis, characterization and treatment of complex diseases is done all at once. There are many types of chemical systems that can be used to build molecular computers. In this project, we explored aptamer displacement reactions. Aptamers are short DNA sequences that can bind specifically to a molecule or protein, the target. In the displacement reaction, another DNA molecule is bound to the aptamer, which is released when the target binds the aptamer. In this case, the released molecule acts as a signal that can trigger further reactions. Aptamer displacement reactions are complex, but form the basis for future drugs that can be used to diagnose and treat patients with complex diseases.
Data: CORDIS, © European Union
Project objective
Our goal is to develop all-DNA structures (protocells) that can act as modulators of the immune system and, in particular, of signaling processes in oncology. Molecular DNA switches that interact with cells via aptamers have been developed and used for drug delivery, cell imaging, and potential therapies. However, there are several advantages of incorporating these swithces into protocells, such as the protection of these circuits against degradation, the ability to create gradients and as a delviery method for in vivo application. DNA protocells that (i) have the ability to recognize proteins and small molecules and (ii) amplify signals and generate output that alters cell physiology have not yet been developed. Realizing these structures requires filling a gap in our knowledge of how of how aptamer reactions network in confinement. We anticipate that by filling these gaps in our knowledge, we will be able to produce a pure DNA protocell that can harbor aptamer-based response networks for modulation of intercelullar communication in the tumor microenvironment.
Original text from CORDIS.
Participants
- JOHANNES GUTENBERG-UNIVERSITAT MAINZ · MainzCoordinatorGermany
- City College of the City University of New York · New York, NyUnited States
Links
- View on CORDIS
- DOI: 10.3030/101111348
- https://ec.europa.eu/research/participants/documents/downloadPublic?documentIds=080166e502d43a4e&appId=PPGMS
- https://ec.europa.eu/research/participants/documents/downloadPublic?documentIds=080166e51b507193&appId=PPGMS
Data: CORDIS, © European Union
