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<dc:title xml:lang="fr">Quantification des affinités PBM/PDZ et de leurs sites modulateurs par des approches expérimentales et informatiques à haut débit</dc:title>
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<dc:subject xml:lang="fr">Interaction domaine-motif</dc:subject>
<dc:subject xml:lang="fr">Modifications post-traductionnelles</dc:subject>
<dc:subject xml:lang="fr">Analyse quantitative d’interactomes</dc:subject>
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<dc:subject xml:lang="en">Domain-motif interaction</dc:subject>
<dc:subject xml:lang="en">Post-translational modifications</dc:subject>
<dc:subject xml:lang="en">Quantitative analysis of interactomes</dc:subject>
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<dcterms:abstract xml:lang="fr">Ce travail a porté sur les domaines PDZ, une famille de domaines globulaires reconnaissant des motifs de liaison aux PDZ (appelés PBM, pour ‘PDZ-Binding Motifs’) généralement situés à l'extrémité C-terminale de leurs protéines partenaires. Les réseaux domaines-motifs sont souvent modulés par des modifications post-traductionnelles réversibles (PTM). Nous avons utilisé des PBM synthétiques simulant différentes conditions: motifs sauvages de diverses longueurs, acétylés, phosphorylés ou portant des mutations ‘imitant’ les PTM. Ces peptides ont été utilisés pour des études d'interaction à l'aide du test ‘Hold-Up’, un test développé à l'origine dans notre laboratoire. Nous avons évalué l'impact de diverses modifications des complexes PBM/PDZ, qui conduisent à un changement global de leur capacité de liaison du PDZ. Ces résultats fournissent des informations quantitatives sur l'effet biologique que de telles modifications pourraient avoir dans le contexte des protéines entières.</dcterms:abstract>
<dcterms:abstract xml:lang="en">This thesis focuses on PDZ domains, a family of globular domains that bind to conserved PDZ-Binding Motifs (called henceforth PBMs) generally situated at the extreme C-terminus of their partner proteins. Domain-motif networks are often modulated by reversible post-translational modifications (PTMs). We used synthetized PBMs to reproduce different conditions, such as a wild-type, acetylation or phosphorylation, addition of extra exosites or residue mimication of PTM in the literature. These peptides were used for interaction studies using the holdup assay, an assay originally developed in our laboratory. We evaluated the impact of diverse modifications of the PBM/PDZ interactions, which led to a global change of the PDZ-binding capability. These results provided quantitative information on the biological effects that such modifications may have in the context of full-length proteins.</dcterms:abstract>
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