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illumizymes SIGNED

Illuminating aptamers and ribozymes for biomolecular tagging and fluorogen activation

Total Cost €

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EC-Contrib. €

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Partnership

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 illumizymes project word cloud

Explore the words cloud of the illumizymes project. It provides you a very rough idea of what is the project "illumizymes" about.

flexibility    complexity    selective    posttranscriptional    restricting    tags    repertoire    sequences    linear    inspired    ligand    living    disease    conformational    binding    toxic    evolution    permeable    reactions    biopolymers    roles    color    latent    relative    noncoding    microscopy    dimensional    rna    fold    introduce    tools    imaging    characterization    vitro    small    naturally    orthogonal    regulators    labels    types    activate    poorly    blocks    cells    ribozymes    catalytic    vivo    add    genome    despite    cellular    consist    fraction    select    illumizymes    structures    systematic    translated    building    functional    stable    cell    limited    layer    regulatory    transcribed    interrogation    bio    labeling    enrichment    modifications    probes    aptamers    encodable    visualization    brightness    manipulation    functions    diverse    ligands    proteins    fixed    composition    rnas    molecular    human    attach    metabolism    genetically    evolve    affinity    selex    bonds    fluorescence    unknown    health    endowed    simplicity    prominent    fluorophores    photostability    extra    exponential    switching    enlighten    surprising    actual    covalent    methodological    chromophores    disciplines   

Project "illumizymes" data sheet

The following table provides information about the project.

Coordinator
JULIUS-MAXIMILIANS-UNIVERSITAT WURZBURG 

Organization address
address: SANDERRING 2
city: WUERZBURG
postcode: 97070
website: http://www.uni-wuerzburg.de

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 Germany [DE]
 Total cost 2˙061˙250 €
 EC max contribution 2˙061˙250 € (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 2016-07-01   to  2021-06-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    JULIUS-MAXIMILIANS-UNIVERSITAT WURZBURG DE (WUERZBURG) coordinator 1˙977˙500.00
2    GEORG-AUGUST-UNIVERSITAT GOTTINGENSTIFTUNG OFFENTLICHEN RECHTS DE (GOTTINGEN) participant 83˙750.00

Map

 Project objective

RNAs are linear biopolymers that consist of only four types of building blocks, but can fold into complex three-dimensional structures that are endowed with selective, high-affinity ligand-binding abilities known as aptamers, and catalytic activities known as ribozymes. Genome projects have brought the surprising insight that a large part of the human genome is transcribed into RNAs, but only a very small fraction is translated into proteins. The actual number of noncoding RNAs with specific functions is currently unknown, but many are considered as prominent regulators of cellular functions. Posttranscriptional modifications of RNA add an extra layer of complexity, but their regulatory roles in RNA metabolism are only poorly understood. Despite the relative simplicity in molecular composition, the available methodological repertoire for manipulation, interrogation and visualization of RNA is rather limited. This project aims to solve the challenge of RNA labeling in both fixed and living cells, using aptamers and ribozymes for RNA imaging and functional characterization. We introduce the term illumizymes for novel tools that attach bio-orthogonal tags and fluorophores to specific RNA sequences, in vitro and in vivo. Ribozymes and aptamers for small, stable, and specific labels will be identified by in vitro selection and systematic evolution of ligands by exponential enrichment (SELEX) to activate the fluorescence of latent chromophores by restricting their conformational flexibility and/or formation of covalent bonds by new bio-orthogonal reactions. Using naturally inspired, cell-permeable and non-toxic ligands, we will specifically select for increased brightness and photostability, and evolve illumizymes into color-switching probes for RNA microscopy. The new genetically encodable RNA devices will find widespread applications in diverse disciplines to enlighten our understanding of cellular RNA functions in health and disease.

 Publications

year authors and title journal last update
List of publications.
2019 Christian Steinmetzger, Irene Bessi, Ann-Kathrin Lenz, Claudia Höbartner
Structure–fluorescence activation relationships of a large Stokes shift fluorogenic RNA aptamer
published pages: 2019, 47, 11538-, ISSN: 0305-1048, DOI: 10.1093/nar/gkz1084
Nucleic Acids Research 2020-01-30
2018 Maksim V. Sednev, Volodymyr Mykhailiuk, Priyanka Choudhury, Julia Halang, Katherine E. Sloan, Markus T. Bohnsack, Claudia Höbartner
N 6 -Methyladenosine-Sensitive RNA-Cleaving Deoxyribozymes
published pages: 15117-15121, ISSN: 1433-7851, DOI: 10.1002/anie.201808745
Angewandte Chemie International Edition 57/46 2019-02-25
2017 Tucker J. Carrocci, Lea Lohe, Matthew J. Ashton, Claudia Höbartner, Aaron A. Hoskins
Debranchase-resistant labeling of RNA using the 10DM24 deoxyribozyme and fluorescent modified nucleotides
published pages: 11992-11995, ISSN: 1359-7345, DOI: 10.1039/c7cc06703h
Chemical Communications 53/88 2019-02-25
2018 Christian Steinmetzger, Navaneethan Palanisamy, Kiran R. Gore, Claudia Höbartner
A Multicolor Large Stokes Shift Fluorogen-Activating RNA Aptamer with Cationic Chromophores
published pages: 5, ISSN: 0947-6539, DOI: 10.1002/chem.201805882
Chemistry - A European Journal weekly 2019-02-25

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