MIcrobe-synthesised DNA NAnostructures for DIsplay-controlled Storage Cartridges

Informacje na temat projektu

MI-DNA DISC

Identyfikator umowy o grant: 101115215

DOI

10.3030/101115215

Data podpisania przez KE 21 Czerwca 2023

Data rozpoczęcia 1 Września 2023

Data zakończenia 31 Sierpnia 2027

Finansowanie w ramach

• The European Innovation Council (EIC)

Koszt całkowity

€ 3 999 506,50

Wkład UE

€ 3 999 506,50

Koordynowany przez

AIT AUSTRIAN INSTITUTE OF TECHNOLOGY GMBH
Austria

Periodic Reporting for period 1 - MI-DNA DISC (MIcrobe-synthesised DNA NAnostructures for DIsplay-controlled Storage Cartridges)

Okres sprawozdawczy: 2023-09-01 do 2024-08-31

Podsumowanie kontekstu i ogólnych celów projektu

The ongoing digitalisation is leading to a massive increase of data generated. Conventional storing technologies can only be upscaled to a certain degree due to increasing material and energy costs. DNA is a promising storing medium due to its high data density and stability. Our vision is to develop a low-cost, energy-efficient, and fast data drive that is able to write, edit, store, and retrieve DNA-based data. The data drive is based on simple and easily available hardware components plus bacterial cells. To achieve this vision, we will exploit bacterial genetic mechanisms that were evolutionarily optimised for billions of years, such as colour-sensitive genetic switches and DNA exchange processes. We have defined two specific objectives to achieve our goal.
The first objective is to create a pipeline that converts digital data into DNA nanostructures with increased biostability compared to conventional duplex DNA.
The second objective is to develop a storing cartridge that uses bacteria for the storage of the DNA-based information.

Prace wykonane od początku projektu do końca okresu sprawozdawczego oraz najważniejsze dotychczasowe rezultaty

In the first year of the project, we started to develop a coding and encoding scheme. To evaluate these process, we have developed a digital twin that simulates the DNA writing and sequencing processes considering writing and sequencing errors as well as mutations in bacteria. In addition, we developed in silico tools to reduce wetlab experiments.
In a second work package, we started to evaluate bacteria that are most suitable for DNA data storage. We have selected three species that are suited for the development of the proof-of-concept as well as long-term storage. Further, we analysed genetic tools to manipulate bacterial DNA processes.

Innowacyjność oraz oczekiwany potencjalny wpływ (w tym dotychczasowe znaczenie społeczno-gospodarcze i szersze implikacje społeczne projektu)

Since we started from a very low TRL (1), no results significantly above the state of the art were achieved in the first year.