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BIOVIB SIGNED

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

Total Cost €

0

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.

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

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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