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Towards a molecular basis of ubiquitin signaling : a dual-scale simulation study of ubiquitin dimers

Towards a molecular basis of ubiquitin signaling : a dual-scale simulation study of ubiquitin dimers

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BERG, Andrej, Oleksandra KUKHARENKO, Martin SCHEFFNER, Christine PETER, 2018. Towards a molecular basis of ubiquitin signaling : a dual-scale simulation study of ubiquitin dimers. In: PLoS computational biology. 14(11), e1006589. eISSN 1553-7358. Available under: doi: 10.1371/journal.pcbi.1006589

@article{Berg2018-11Towar-44400, title={Towards a molecular basis of ubiquitin signaling : a dual-scale simulation study of ubiquitin dimers}, year={2018}, doi={10.1371/journal.pcbi.1006589}, number={11}, volume={14}, journal={PLoS computational biology}, author={Berg, Andrej and Kukharenko, Oleksandra and Scheffner, Martin and Peter, Christine}, note={Article Number: e1006589} }

Peter, Christine Scheffner, Martin 2018-12-21T10:35:26Z Berg, Andrej 2018-12-21T10:35:26Z Peter, Christine Kukharenko, Oleksandra eng Berg, Andrej Scheffner, Martin Kukharenko, Oleksandra Towards a molecular basis of ubiquitin signaling : a dual-scale simulation study of ubiquitin dimers 2018-11 Covalent modification of proteins by ubiquitin or ubiquitin chains is one of the most prevalent post-translational modifications in eukaryotes. Different types of ubiquitin chains are assumed to selectively signal respectively modified proteins for different fates. In support of this hypothesis, structural studies have shown that the eight possible ubiquitin dimers adopt different conformations. However, at least in some cases, these structures cannot sufficiently explain the molecular basis of the selective signaling mechanisms. This indicates that the available structures represent only a few distinct conformations within the entire conformational space adopted by a ubiquitin dimer. Here, molecular simulations on different levels of resolution can complement the structural information. We have combined exhaustive coarse grained and atomistic simulations of all eight possible ubiquitin dimers with a suitable dimensionality reduction technique and a new method to characterize protein-protein interfaces and the conformational landscape of protein conjugates. We found that ubiquitin dimers exhibit characteristic linkage type-dependent properties in solution, such as interface stability and the character of contacts between the subunits, which can be directly correlated with experimentally observed linkage-specific properties.<br /><br />Author summary<br />Post-translational modification of proteins by covalent attachment of ubiquitin is a key cellular process, regulating for example the fate and recycling of proteins. We present a new method to combine multiscale simulation with advanced analysis methods to characterize the states of ubiquitin-ubiquitin conjugates. We found that the linkage position affects the conformational space of ubiquitin dimers, determining the number and stability of relevant states, the character of subunit contacts and the nature of the surface exposed to possible binding partners. terms-of-use

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