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...

Full description

Bibliographic Details
Main Authors: Katrine Bugge, Inna Brakti, Catarina B. Fernandes, Jesper E. Dreier, Jeppe E. Lundsgaard, Johan G. Olsen, Karen Skriver, Birthe B. Kragelund
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-06-01
Series:Frontiers in Molecular Biosciences
Subjects:
IDP
Online Access:https://www.frontiersin.org/article/10.3389/fmolb.2020.00110/full
id doaj-c6455c1ccc2e408fa283986206056610
record_format Article
spelling 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
collection 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
work_keys_str_mv AT katrinebugge interactionsbydisorderamatterofcontext
AT katrinebugge interactionsbydisorderamatterofcontext
AT innabrakti interactionsbydisorderamatterofcontext
AT innabrakti interactionsbydisorderamatterofcontext
AT catarinabfernandes interactionsbydisorderamatterofcontext
AT catarinabfernandes interactionsbydisorderamatterofcontext
AT jesperedreier interactionsbydisorderamatterofcontext
AT jesperedreier interactionsbydisorderamatterofcontext
AT jeppeelundsgaard interactionsbydisorderamatterofcontext
AT jeppeelundsgaard interactionsbydisorderamatterofcontext
AT johangolsen interactionsbydisorderamatterofcontext
AT johangolsen interactionsbydisorderamatterofcontext
AT karenskriver interactionsbydisorderamatterofcontext
AT birthebkragelund interactionsbydisorderamatterofcontext
AT birthebkragelund interactionsbydisorderamatterofcontext
_version_ 1724755586349793280