Interactions by Disorder – A Matter of Context
Living organisms depend on timely and organized interactions between proteins linked in interactomes of high complexity. The recent increased precision by which protein interactions can be studied, and the enclosure of intrinsic structural disorder, suggest that it is time to zoom out and embrace pr...
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doaj-c6455c1ccc2e408fa2839862060566102020-11-25T02:46:58ZengFrontiers Media S.A.Frontiers in Molecular Biosciences2296-889X2020-06-01710.3389/fmolb.2020.00110545494Interactions by Disorder – A Matter of ContextKatrine Bugge0Katrine Bugge1Inna Brakti2Inna Brakti3Catarina B. Fernandes4Catarina B. Fernandes5Jesper E. Dreier6Jesper E. Dreier7Jeppe E. Lundsgaard8Jeppe E. Lundsgaard9Johan G. Olsen10Johan G. Olsen11Karen Skriver12Birthe B. Kragelund13Birthe B. Kragelund14REPIN, Department of Biology, University of Copenhagen, Copenhagen, DenmarkStructural Biology and NMR Laboratory, Department of Biology, University of Copenhagen, Copenhagen, DenmarkREPIN, Department of Biology, University of Copenhagen, Copenhagen, DenmarkStructural Biology and NMR Laboratory, Department of Biology, University of Copenhagen, Copenhagen, DenmarkREPIN, Department of Biology, University of Copenhagen, Copenhagen, DenmarkStructural Biology and NMR Laboratory, Department of Biology, University of Copenhagen, Copenhagen, DenmarkREPIN, Department of Biology, University of Copenhagen, Copenhagen, DenmarkStructural Biology and NMR Laboratory, Department of Biology, University of Copenhagen, Copenhagen, DenmarkREPIN, Department of Biology, University of Copenhagen, Copenhagen, DenmarkStructural Biology and NMR Laboratory, Department of Biology, University of Copenhagen, Copenhagen, DenmarkREPIN, Department of Biology, University of Copenhagen, Copenhagen, DenmarkStructural Biology and NMR Laboratory, Department of Biology, University of Copenhagen, Copenhagen, DenmarkREPIN, Department of Biology, University of Copenhagen, Copenhagen, DenmarkREPIN, Department of Biology, University of Copenhagen, Copenhagen, DenmarkStructural Biology and NMR Laboratory, Department of Biology, University of Copenhagen, Copenhagen, DenmarkLiving organisms depend on timely and organized interactions between proteins linked in interactomes of high complexity. The recent increased precision by which protein interactions can be studied, and the enclosure of intrinsic structural disorder, suggest that it is time to zoom out and embrace protein interactions beyond the most central points of physical encounter. The present paper discusses protein–protein interactions in the view of structural disorder with an emphasis on flanking regions and contexts of disorder-based interactions. Context constitutes an overarching concept being of physicochemical, biomolecular, and physiological nature, but it also includes the immediate molecular context of the interaction. For intrinsically disordered proteins, which often function by exploiting short linear motifs, context contributes in highly regulatory and decisive manners and constitute a yet largely unrecognized source of interaction potential in a multitude of biological processes. Through selected examples, this review emphasizes how multivalency, charges and charge clusters, hydrophobic patches, dynamics, energetic frustration, and ensemble redistribution of flanking regions or disordered contexts are emerging as important contributors to allosteric regulation, positive and negative cooperativity, feedback regulation and negative selection in binding. The review emphasizes that understanding context, and in particular the role the molecular disordered context and flanking regions take on in protein interactions, constitute an untapped well of energetic modulation potential, also of relevance to drug discovery and development.https://www.frontiersin.org/article/10.3389/fmolb.2020.00110/fullIDPSLiMprotein interactionscontextflanking regionintrinsically disordered proteins |
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DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Katrine Bugge Katrine Bugge Inna Brakti Inna Brakti Catarina B. Fernandes Catarina B. Fernandes Jesper E. Dreier Jesper E. Dreier Jeppe E. Lundsgaard Jeppe E. Lundsgaard Johan G. Olsen Johan G. Olsen Karen Skriver Birthe B. Kragelund Birthe B. Kragelund |
spellingShingle |
Katrine Bugge Katrine Bugge Inna Brakti Inna Brakti Catarina B. Fernandes Catarina B. Fernandes Jesper E. Dreier Jesper E. Dreier Jeppe E. Lundsgaard Jeppe E. Lundsgaard Johan G. Olsen Johan G. Olsen Karen Skriver Birthe B. Kragelund Birthe B. Kragelund Interactions by Disorder – A Matter of Context Frontiers in Molecular Biosciences IDP SLiM protein interactions context flanking region intrinsically disordered proteins |
author_facet |
Katrine Bugge Katrine Bugge Inna Brakti Inna Brakti Catarina B. Fernandes Catarina B. Fernandes Jesper E. Dreier Jesper E. Dreier Jeppe E. Lundsgaard Jeppe E. Lundsgaard Johan G. Olsen Johan G. Olsen Karen Skriver Birthe B. Kragelund Birthe B. Kragelund |
author_sort |
Katrine Bugge |
title |
Interactions by Disorder – A Matter of Context |
title_short |
Interactions by Disorder – A Matter of Context |
title_full |
Interactions by Disorder – A Matter of Context |
title_fullStr |
Interactions by Disorder – A Matter of Context |
title_full_unstemmed |
Interactions by Disorder – A Matter of Context |
title_sort |
interactions by disorder – a matter of context |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Molecular Biosciences |
issn |
2296-889X |
publishDate |
2020-06-01 |
description |
Living organisms depend on timely and organized interactions between proteins linked in interactomes of high complexity. The recent increased precision by which protein interactions can be studied, and the enclosure of intrinsic structural disorder, suggest that it is time to zoom out and embrace protein interactions beyond the most central points of physical encounter. The present paper discusses protein–protein interactions in the view of structural disorder with an emphasis on flanking regions and contexts of disorder-based interactions. Context constitutes an overarching concept being of physicochemical, biomolecular, and physiological nature, but it also includes the immediate molecular context of the interaction. For intrinsically disordered proteins, which often function by exploiting short linear motifs, context contributes in highly regulatory and decisive manners and constitute a yet largely unrecognized source of interaction potential in a multitude of biological processes. Through selected examples, this review emphasizes how multivalency, charges and charge clusters, hydrophobic patches, dynamics, energetic frustration, and ensemble redistribution of flanking regions or disordered contexts are emerging as important contributors to allosteric regulation, positive and negative cooperativity, feedback regulation and negative selection in binding. The review emphasizes that understanding context, and in particular the role the molecular disordered context and flanking regions take on in protein interactions, constitute an untapped well of energetic modulation potential, also of relevance to drug discovery and development. |
topic |
IDP SLiM protein interactions context flanking region intrinsically disordered proteins |
url |
https://www.frontiersin.org/article/10.3389/fmolb.2020.00110/full |
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