Objective
Nature makes use of covalent additions of functional groups to proteins for regulating essential processes like cellular signalling and protein folding/degradation. Most of these post-translational modifications (PTMs) are enzymatically-reversible, with the coupled catalytic processes being fulfilled by antagonistic enzymes (e.g. methylase-demethylase pair). This dynamic behaviour allows for the correct metabolic equilibrium, as an unbalanced PTM-machinery is indicative of some severe diseases. Such a complex auto-regulated system is the result of millions of years of evolution that has allowed for highly efficient and site-selective functionalizations. Nevertheless, selective covalent bond formation in a substrate with multiple competitive sites is an intricate endeavour in the absence of auxiliary enzymes or other sacrificial agents. Dynamic Covalent Chemistry could be a major asset for overcoming this research bottleneck, as the reversible nature of the reactions involved can drive the functionalization to the most thermodynamically favoured site.
Most proteins contain Lys (K) residues with terminal amino groups suitable for derivatization. In particular, histone K-PTMs are crucial for controlling gene expression, with the most common modifications being acetylation and methylation. The proposed work will explore the reversible modification of histones using aldehydes that contain within their structure the functional groups required for the recognition by biological readers. For instance, aldehydes with carboxylate and trimethylated ammonium groups will be examined to mimic naturally occurring K-succinylation and K-trimethylation. This approach is still unexploited due to the lability of imine bonds in physiological water. However, several important biological processes are governed by the formation of imino/iminium reversible bonds with pyridoxal-5-phosphate (PLP) derivatives, inferring that this sort of chemistry is possible in protein microenvironments.
Fields of science (EuroSciVoc)
CORDIS classifies projects with EuroSciVoc, a multilingual taxonomy of fields of science, through a semi-automatic process based on NLP techniques. See: The European Science Vocabulary.
CORDIS classifies projects with EuroSciVoc, a multilingual taxonomy of fields of science, through a semi-automatic process based on NLP techniques. See: The European Science Vocabulary.
- natural sciences chemical sciences organic chemistry aldehydes
- natural sciences biological sciences biochemistry biomolecules proteins enzymes
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Keywords
Project’s keywords as indicated by the project coordinator. Not to be confused with the EuroSciVoc taxonomy (Fields of science)
Project’s keywords as indicated by the project coordinator. Not to be confused with the EuroSciVoc taxonomy (Fields of science)
Programme(s)
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Multi-annual funding programmes that define the EU’s priorities for research and innovation.
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HORIZON.1.2 - Marie Skłodowska-Curie Actions (MSCA)
MAIN PROGRAMME
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Topic(s)
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Calls for proposals are divided into topics. A topic defines a specific subject or area for which applicants can submit proposals. The description of a topic comprises its specific scope and the expected impact of the funded project.
Funding Scheme
Funding scheme (or “Type of Action”) inside a programme with common features. It specifies: the scope of what is funded; the reimbursement rate; specific evaluation criteria to qualify for funding; and the use of simplified forms of costs like lump sums.
Funding scheme (or “Type of Action”) inside a programme with common features. It specifies: the scope of what is funded; the reimbursement rate; specific evaluation criteria to qualify for funding; and the use of simplified forms of costs like lump sums.
HORIZON-TMA-MSCA-PF-EF - HORIZON TMA MSCA Postdoctoral Fellowships - European Fellowships
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Call for proposal
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Procedure for inviting applicants to submit project proposals, with the aim of receiving EU funding.
(opens in new window) HORIZON-MSCA-2023-PF-01
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67081 STRASBOURG
France
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