Project description
Megakines as a tool for the structural analysis of receptor:chemokine complexes
Chemokines are small, secreted cytokines that activate membrane receptors of the G protein-coupled receptor superfamily. The chemokine–receptor interactions control many physiological processes and are implicated in many pathologies, including atherosclerosis, inflammatory diseases, HIV infection and cancer. The interactions of 50 chemokines and 20 receptors identified in humans require precise orchestration as a chemokine may bind to several receptors, while a single chemokine receptor has multiple ligands. Cryo-electron microscopy is a ground-breaking technique for elucidating molecular structures, but the analysis of small proteins like receptor:chemokine complexes is still challenging. The EU-funded MEGAKINE project proposes an innovative approach to increase chemokine size through a rigid insertion into a bulky scaffold protein, creating megakines to facilitate the structural analysis of chemokine receptors.
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.
Fields of science
- medical and health scienceshealth sciencesinflammatory diseases
- medical and health sciencesclinical medicinecardiologycardiovascular diseasesarteriosclerosis
- natural sciencesbiological sciencesbiochemistrybiomoleculesproteins
- medical and health scienceshealth sciencesinfectious diseasesRNA virusesHIV
- medical and health sciencesbasic medicinepathology
Keywords
Programme(s)
Funding Scheme
MSCA-IF - Marie Skłodowska-Curie Individual Fellowships (IF)Coordinator
1445 Strassen
Luxembourg