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Exploring the molecular grammar of IDP assembly and condensation at ultra-high throughput

Project description

Unravelling the mysteries of intrinsically disordered proteins

Intrinsically disordered proteins (IDPs) lack a stable, well-defined three-dimensional structure and adopt multiple conformations, often with a high degree of flexibility. IDPs also perform a range of important biological functions, such as signalling, transcription and cell division. Despite their significance, IDPs have long been considered a mystery in the field of protein science. Funded by the European Research Council, the EMMA project aims to unravel this mystery. Using advanced experimental biophysics, machine learning algorithms and molecular simulations, EMMA seeks a quantitative understanding of how the structure and interactions of IDPs are defined by their amino acid sequence. It will develop a novel experimental strategy that will allow studying the behavior of millions of amino acid sequences simultaneously.

Objective

The last years have seen unprecedented breakthroughs in protein structural biology, with the resolution revolution in cryo-electron microscopy and the release of AlphaFold. The combination of advanced experimental structural biology, machine learning algorithms and molecular simulations has put the fully quantitative description of how the structure and interactions of folded proteins are defined by their amino acid sequence within close reach.
This leaves us with a final frontier in protein science, namely to achieve a similar level of understanding for intrinsically disordered proteins (IDPs). The energy landscapes of IDPs often comprise a multitude of nearly isoenergetic states, that include assembled forms, such as amyloid fibrils and liquid condensate droplets.
Much effort has been spent in order to achieve an understanding of the molecular grammar of IDP assembly and condensation, i.e. how amino acid sequence defines both kinetics and thermodynamics of these processes. Current state of the art is to evaluate a few dozens of sequence perturbations quantitatively in vitro.
In EMMA, I propose to develop a fundamentally new approach that will ultimately allow to improve on current methods by more than 8 orders of magnitude. This ground-breaking improvement will be achieved by exploiting the power of mRNA display, in which the biophysical behavior of each individual sequence within large libraries of protein-mRNA constructs can be evaluated in a “one pot” reaction. We will combine quantitative screening of the energetics of liquid condensate droplet formation of up to 10^10 sequences by mRNA display with a multiparametric biophysical toolbox that allows the key thermodynamic and kinetic parameters of binding and assembly to be evaluated for thousands of selected sequence variants.
EMMA will transform our ability to probe the mechanisms and interrelationships of the interactions and assembly processes that define IDP function and disease-related malfunction.

Fields of science (EuroSciVoc)

Keywords

Programme(s)

Topic(s)

Funding Scheme

HORIZON-ERC - HORIZON ERC Grants

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Call for proposal

(opens in new window) ERC-2022-COG

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Host institution

DANMARKS TEKNISKE UNIVERSITET
Net EU contribution
€ 1 995 554,00
Address
ANKER ENGELUNDS VEJ 101
2800 Kongens Lyngby
Denmark
Region
Danmark Hovedstaden Københavns omegn
Activity type
Higher or Secondary Education Establishments
Links
Total cost
€ 1 995 554,00

Beneficiaries (1)