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Glycan foldamers: designing oligosaccharides to build three-dimensional architectures

Project description

Paving the way to rational design of glycan foldamers

Biopolymers, long-chain molecules made of common building blocks, include proteins, carbohydrates and nucleic acids. The formation of complex 3D architectures from peptides and nucleic acids, respectively, is well-characterised, enabling the construction of similar molecules, "foldamers," by synthetic chemists. The same is not true of carbohydrate-based polymers, yet polysaccharides or glycans may offer even greater opportunity for the generation of 3D structures. The ERC-funded GLYCOFOLD project will investigate carbohydrate structure, design new methods to stabilise conformations, and implement protocols for systematic structural analysis. The project’s state-of-the-art synthetic platforms and analytical techniques could open the door to a new field of carbohydrate-based foldamers akin to peptide-based ones.

Objective

Natural biopolymers have inspired the development of synthetic analogues – i.e. foldamers – capable of adopting defined conformations and forming programmable three-dimensional architectures. These compounds are mainly based on peptides and nucleic acids, that are well understood at the molecular level. The diversity, intrinsic chirality, and ability to generate hierarchical assemblies suggest that carbohydrates hold an even larger potential for the generation of three-dimensional structures. However, the complexity of carbohydrate synthesis and structural analysis have prevented access to synthetic carbohydrates capable of adopting defined geometries.
I propose the creation of carbohydrate foldamers capable of 1) adopting rigid secondary structures and 2) assembling into supramolecular architectures. To achieve these goals, we will address fundamental questions related to carbohydrate structure, design new methods to stabilize particular conformations, and we will implement protocols for systematic structural analysis. State-of-the-art synthetic platforms (i.e. automated glycan assembly) and analytical techniques (i.e. NMR spectroscopy, microED, and single molecule imaging) will be the tools to complete this ambitious project. My group has proved to be very successful at gaining a basic understanding of carbohydrate structure and aggregation. Building upon these preliminary results, I aim to develop programmable carbohydrate architectures, which have the potential to open a new field of carbohydrate and supramolecular chemistry.
Analogous to the birth of a new field after the discovery of peptide-based foldamers, carbohydrate foldamers could find applications in several areas, including material science, biology, and catalysis. Moreover, carbohydrate foldamers will expand our understanding of carbohydrate structures and interactions, and new analytical protocols will standardize the characterization of carbohydrate materials.

Fields of science (EuroSciVoc)

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Keywords

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Programme(s)

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Topic(s)

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Funding Scheme

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HORIZON-ERC - HORIZON ERC Grants

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Call for proposal

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(opens in new window) ERC-2022-STG

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Host institution

MAX-PLANCK-GESELLSCHAFT ZUR FORDERUNG DER WISSENSCHAFTEN EV
Net EU contribution

Net EU financial contribution. The sum of money that the participant receives, deducted by the EU contribution to its linked third party. It considers the distribution of the EU financial contribution between direct beneficiaries of the project and other types of participants, like third-party participants.

€ 1 499 956,00
Address
HOFGARTENSTRASSE 8
80539 MUNCHEN
Germany

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Region
Bayern Oberbayern München, Kreisfreie Stadt
Activity type
Research Organisations
Links
Total cost

The total costs incurred by this organisation to participate in the project, including direct and indirect costs. This amount is a subset of the overall project budget.

€ 1 499 956,25

Beneficiaries (1)

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