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RNA ORIGAMI SIGNED

RNA-protein Nanostructures for Synthetic Biology

Total Cost €

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EC-Contrib. €

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Partnership

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Project "RNA ORIGAMI" data sheet

The following table provides information about the project.

Coordinator
AARHUS UNIVERSITET 

Organization address
address: NORDRE RINGGADE 1
city: AARHUS C
postcode: 8000
website: www.au.dk

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
telephone: n.a.
fax: n.a.

 Coordinator Country Denmark [DK]
 Project website http://andersen-lab.dk/
 Total cost 1˙999˙935 €
 EC max contribution 1˙999˙935 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2015-CoG
 Funding Scheme ERC-COG
 Starting year 2016
 Duration (year-month-day) from 2016-04-01   to  2021-03-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    AARHUS UNIVERSITET DK (AARHUS C) coordinator 1˙999˙935.00

Map

 Project objective

Synthetic biology aims at re-engineering organisms for practical applications by designing novel biomolecular components, networks, and pathways. The field is expected to lead to cheaper drugs, sustainable fuel production, efficient diagnosis and targeted therapies for diseases. However, a major obstacle to achieve these goals is our limited ability to rationally design biomolecular structure and function. By contrast, the field of DNA nanotechnology has so far demonstrated an unprecedented ability to design and self-assemble well-defined molecular shapes, although the production method of thermal annealing is not compatible with cells. We have recently demonstrated a breakthrough method, called RNA origami, which allows the design of RNA molecules that fold into well-defined nanoscale shapes during their synthesis by an RNA polymerase. In this proposal I aim at extending this technology to produce RNA-protein nanostructures and at demonstrating their application in synthetic biology. My primary scientific hypothesis is that understanding the folding process during synthesis will help us to design nanostructures that can be produced in cells. I will design a general RNA-protein architecture that is compatible with folding during synthesis. I will investigate folding kinetics to be able to design and program the dynamical folding process. Based on this, RNA-protein nanostructures will be designed, expressed in cells, and verified, for the formation of the desired shapes. We will develop new functionalities by both rational design and selection approaches with the aim of obtaining multivalent-binding and switching properties. Finally, the functional RNA-protein nanostructures will be applied in proof-of-concept experiments to demonstrate efficient, multivalent targeting of subcellular structures, biosensing of a variety of intracellular analytes, metabolic channeling of biosynthesis pathways, and complex control of transcriptional networks.

 Publications

year authors and title journal last update
List of publications.
2017 Yossi Weizmann, Ebbe Sloth Andersen
RNA nanotechnology—The knots and folds of RNA nanoparticle engineering
published pages: 930-935, ISSN: 0883-7694, DOI: 10.1557/mrs.2017.277
MRS Bulletin 42/12 2019-10-09
2017 Guido Grossi, Andreas Jaekel, Ebbe Sloth Andersen, Barbara Saccà
Enzyme-functionalized DNA nanostructures as tools for organizing and controlling enzymatic reactions
published pages: 920-924, ISSN: 0883-7694, DOI: 10.1557/mrs.2017.269
MRS Bulletin 42/12 2019-10-09
2017 Guido Grossi, Mette Dalgaard Ebbesen Jepsen, Jørgen Kjems, Ebbe Sloth Andersen
Control of enzyme reactions by a reconfigurable DNA nanovault
published pages: , ISSN: 2041-1723, DOI: 10.1038/s41467-017-01072-8
Nature Communications 8/1 2019-10-09
2019 Aradhana Chopra, Sandra Sagredo, Guido Grossi, Ebbe Andersen, Friedrich Simmel
Out-of-Plane Aptamer Functionalization of RNA Three-Helix Tiles
published pages: 507, ISSN: 2079-4991, DOI: 10.3390/nano9040507
Nanomaterials 9/4 2019-06-07
2019 Abhichart Krissanaprasit, Carson Key, Michael Fergione, Kristen Froehlich, Sahil Pontula, Matthew Hart, Pedro Carriel, Jørgen Kjems, Ebbe Sloth Andersen, Thomas H. LaBean
Genetically Encoded, Functional Single‐Strand RNA Origami: Anticoagulant
published pages: 1808262, ISSN: 0935-9648, DOI: 10.1002/adma.201808262
Advanced Materials 31/21 2019-06-07

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