Menu
MapConnectionsTopicsBulgariaThe Night (K-TRIO)Marie Skłodowska-CurieFor studentsFor teachersMethodologySurprise me
H2020Individual fellowship2021–2023

MEGAKINE · Megakines - novel tools for structural insight into receptor:chemokine complexes

Horizon 2020 — Marie Skłodowska-Curie Actions

Duration
2021-09-01 → 2023-08-31
EU contribution
€178,320
Participants
1
Scheme
MSCA-IF

Lines connect the coordinator with its partners.

Results in brief

Megakines - novel tools for structural insight into receptor:chemokine complexes

Chemokines are small, secreted cytokines that activate membrane receptors belonging to the G protein-coupled receptor (GPCR) superfamily. The chemokine-receptor interactions control crucial physiological processes, but are also implicated in many pathologies, including atherosclerosis, inflammatory diseases, HIV infection or cancer, and hold therefore a great potential for therapeutic intervention. Yet, although GPCRs are the target of about one third of currently marketed drugs, only three of them act on chemokine receptors, essentially due to poor structural understanding of the intricate interactions with their ligands. Indeed, about 50 chemokines and 20 receptors have been identified in humans. Their interactions require precise orchestration, as a chemokine may bind to several receptors, while a single chemokine receptor has multiple ligands. However, the structural determinants dictating ligand specificity and receptor activation remain elusive. Lately, cryo-EM has emerged as a ground-breaking technique for revealing molecular structures but despite recent advancements, analysis of small proteins like receptor:chemokine complexes (~50 kDa) is still challenging. To address these difficulties and limitations, our ambition is to engineer a novel and generic tool to facilitate structural studies of chemokine receptors in complexes with their biological ligands using cryo-EM. For this purpose, we propose to generate chemokine-based chimeric proteins, called Megakines. To prove this concept and assess its applicability in structural biology, we chose to first reformat the well-characterized chemokine CCL5 and investigate its functionality towards two clinically relevant receptors, CCR5 and ACKR2.

Data: CORDIS, © European Union

Project objective

Chemokines are small, secreted cytokines that activate membrane receptors belonging to the G protein-coupled receptor (GPCR) superfamily. The chemokine-receptor interactions control crucial physiological processes, but are also implicated in many pathologies, including atherosclerosis, inflammatory diseases, HIV infection or cancer, and hold a great potential for therapeutic intervention. Yet, although GPCRs are the target of about one third of currently marketed drugs, only three of them act on chemokine receptors, essentially due to poor structural understanding of the intricate interactions with their ligands. Indeed, about 50 chemokines and 20 receptors have been identified in humans. Their interactions require precise orchestration, as a chemokine may bind to several receptors, while a single chemokine receptor has multiple ligands. However, the structural determinants dictating ligand specificity and receptor activation remain elusive. Lately, cryo-EM has emerged as a ground-breaking technique for elucidating molecular structures but despite recent advancements, analysis of small proteins like receptor:chemokine complexes (∼50 kDa) is still challenging. In this project, we propose an innovative approach to increase the chemokine size, without altering its functionality, through a rigid insertion into a bulky scaffold protein. Such enlarged chemokines, called Megakines, will facilitate structural analysis of chemokine receptors.To prove this concept, we will first reformat the well-characterized chemokine CCL5 and use it in structural/functional studies with two clinically relevant receptors, CCR5 and ACKR2. The achievement of this project relies on the multidisciplinary combination of the excellent expertise in the chemokine field of the host laboratory and the protein engineering skills of the applicant. The proposed Megakine technology has the potential to revolutionize cryo-EM studies of chemokine receptors and facilitate the therapeutic development.

Original text from CORDIS.

Participants

  • LUXEMBOURG INSTITUTE OF HEALTH · StrassenCoordinatorLuxembourg

Links

Data: CORDIS, © European Union