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BIOVIB SIGNED

Electric Interactions and Structural Dynamics of Hydrated Biomolecules Mapped by Ultrafast Vibrational Probes

Total Cost €

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EC-Contrib. €

0

Partnership

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 BIOVIB project word cloud

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

retarded    atmosphere    interactions    definition    dynamics    calibrates    separates    paradigm    double    structure    gives    external    terahertz    versus    channels    probes    biomolecules    time    nanometer    stranded    site    mapping    stark    absolute    length    interface    hydration    influenced    atmospheres    barely    water    covalent    spatial    single    scientific    holds    secondary    ray    experiments    introduces    fundamental    scales    dipolar    mechanisms    forces    function    fluctuating    scattering    strengths    tertiary    charge    aqueous    unravel    biological    local    dna    vibrational    shift    composition    ground    breaking    noninvasive    exist    ions    folding    genuine    structures    environment    electric    molecular    direct    theoretical    biomolecular    act    outer    instantaneous    ion    solvated    interplay    quantitative    stabilizing    discerning    sensitive    structurally    magnesium    frequencies    excitations    contributions    presently    sub    spectroscopy    milliseconds    strength    resolved    levels    rhodopsins    channel    multidimensional    separated    thz    bound    molecules    transmembrane    shell    fluctuation    dynamically    rna   

Project "BIOVIB" data sheet

The following table provides information about the project.

Coordinator
FORSCHUNGSVERBUND BERLIN EV 

Organization address
address: RUDOWER CHAUSSEE 17
city: BERLIN
postcode: 12489
website: www.fv-berlin.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˙330˙492 €
 EC max contribution 2˙330˙492 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2018-ADG
 Funding Scheme ERC-ADG
 Starting year 2019
 Duration (year-month-day) from 2019-05-01   to  2024-04-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    FORSCHUNGSVERBUND BERLIN EV DE (BERLIN) coordinator 2˙330˙492.00

Map

 Project objective

Biomolecules exist in an aqueous environment of dipolar water molecules and solvated ions. Their structure and biological function are strongly influenced by electric interactions with the fluctuating water shell and ion atmosphere. Understanding such interactions at the molecular level is a major scientific challenge; presently, their strengths, spatial range and interplay with other non-covalent interactions are barely known. Going far beyond existing methods, this project introduces the new paradigm of a direct time-resolved mapping of molecular electric forces on sub-nanometer length scales and at the genuine terahertz (THz) fluctuation frequencies. Vibrational excitations of biomolecules at the interface to the water shell act as sensitive noninvasive probes of charge dynamics and local electric fields. The new method of time resolved vibrational Stark shift spectroscopy with THz external fields calibrates vibrational frequencies as a function of absolute field strength and separates instantaneous from retarded environment fields. Based on this knowledge, multidimensional vibrational spectroscopy gives quantitative insight in the biomolecular response to electric fields, discerning contributions from water and ions in a site-specific way. The experiments and theoretical analysis focus on single- and double-stranded RNA and DNA structures at different hydration levels and with ion atmospheres of controlled composition, structurally characterized by x-ray scattering. As a ground-breaking open problem, the role of magnesium and other ions in RNA structure definition and folding will be addressed by following RNA folding processes with vibrational probes up to milliseconds. The impact of site-bound versus outer ions will be dynamically separated to unravel mechanisms stabilizing secondary and tertiary RNA structures. Beyond RNA research, the present approach holds strong potential for fundamental insight in transmembrane ion channels and channel rhodopsins.

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The information about "BIOVIB" are provided by the European Opendata Portal: CORDIS opendata.

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