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NMR Spectroscopy of very large complexes: the atomic details of the mRNA degradation machinery

Objectif

The cellular environment is extremely complex and contains thousands of different bio-molecules. To determine how these bio-molecules assemble into a highly organized molecular system has remained a major challenge. Here, we aim to unravel how dozens of proteins assemble into a large molecular machinery that degrades mRNA in an efficient and regulated manner.

On an atomic level, we will determine the static structures of the enzymes involved in the mRNA degradation pathways. In parallel, we will develop and exploit novel methods in NMR spectroscopy to correlate molecular motions with catalytic activity. Especially for the 450 kDa eukaryotic exosome complex, these studies will significantly push the limits of what is currently achievable. On a molecular level, we will reconstitute the mRNA degradation machinery from purified components in a stepwise manner. In this challenging approach, we will use NMR spectroscopy to follow how the enzymes engage in a network of interactions that regulate the mRNA degradation process. These studies will also provide us with the unique possibility to reproduce complex cellular behavior in a well defined and easy to manipulate in vitro system. On a microscopic level the mRNA degradation machinery assembles into cytoplasmic processing bodies. The role of these conserved cellular foci is a matter of debate and we aim to determine both the atomic details that result in this self-organization as well as the catalytic advantages that result from this clustering.

Our study will provide a very detailed and accurate description of how essential and central molecular processes in mRNA degradation are regulated and modulated. The level of detail that we aim to achieve is currently not available for any cellular pathway of such complexity. In that regard, our projects also provide knowledge and methodology required to study additional and complex cellular functions.

Appel à propositions

ERC-2013-CoG
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Régime de financement

ERC-CG - ERC Consolidator Grants

Institution d’accueil

UNIVERSITAET REGENSBURG
Contribution de l’UE
€ 1 089 318,89
Adresse
UNIVERSITATSSTRASSE 31
93053 Regensburg
Allemagne

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Région
Bayern Oberpfalz Regensburg, Kreisfreie Stadt
Type d’activité
Higher or Secondary Education Establishments
Contact administratif
Matthias Köhler (Dr.)
Chercheur principal
Remco Sprangers (Dr.)
Liens
Coût total
Aucune donnée

Bénéficiaires (2)