Extreme Fuzziness: Direct Interactions between Two IDPs

Protein interactions involving intrinsically disordered proteins (IDPs) greatly extend the range of binding mechanisms available to proteins. In interactions employing coupled folding and binding, IDPs undergo disorder-to-order transitions to form a complex with a well-defined structure. In many oth...

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Main Authors: Wenning Wang, Dongdong Wang
Format: Article
Language:English
Published: MDPI AG 2019-02-01
Series:Biomolecules
Subjects:
Online Access:https://www.mdpi.com/2218-273X/9/3/81
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spelling doaj-960861db88bb4651b9e721c0df0f85422020-11-25T01:57:12ZengMDPI AGBiomolecules2218-273X2019-02-01938110.3390/biom9030081biom9030081Extreme Fuzziness: Direct Interactions between Two IDPsWenning Wang0Dongdong Wang1Department of Chemistry, Institute of Biomedical Sciences and Multiscale Research Institute of Complex Systems, Fudan University, Shanghai 200438, ChinaDepartment of Chemistry, Institute of Biomedical Sciences and Multiscale Research Institute of Complex Systems, Fudan University, Shanghai 200438, ChinaProtein interactions involving intrinsically disordered proteins (IDPs) greatly extend the range of binding mechanisms available to proteins. In interactions employing coupled folding and binding, IDPs undergo disorder-to-order transitions to form a complex with a well-defined structure. In many other cases, IDPs retain structural plasticity in the final complexes, which have been defined as the fuzzy complexes. While a large number of fuzzy complexes have been characterized with variety of fuzzy patterns, many of the interactions are between an IDP and a structured protein. Thus, whether two IDPs can interact directly to form a fuzzy complex without disorder-to-order transition remains an open question. Recently, two studies of interactions between IDPs (4.1G-CTD/NuMA and H1/ProTα) have found a definite answer to this question. Detailed characterizations combined with nuclear magnetic resonance (NMR), single-molecule Förster resonance energy transfer (smFRET) and molecular dynamics (MD) simulation demonstrate that direct interactions between these two pairs of IDPs do form fuzzy complexes while retaining the conformational dynamics of the isolated proteins, which we name as the extremely fuzzy complexes. Extreme fuzziness completes the full spectrum of protein-protein interaction modes, suggesting that a more generalized model beyond existing binding mechanisms is required. Previous models of protein interaction could be applicable to some aspects of the extremely fuzzy interactions, but in more general sense, the distinction between native and nonnative contacts, which was used to understand protein folding and binding, becomes obscure. Exploring the phenomenon of extreme fuzziness may shed new light on molecular recognition and drug design.https://www.mdpi.com/2218-273X/9/3/81intrinsic disordered proteinextremely fuzzy complexprotein interactionbinding mechanism
collection DOAJ
language English
format Article
sources DOAJ
author Wenning Wang
Dongdong Wang
spellingShingle Wenning Wang
Dongdong Wang
Extreme Fuzziness: Direct Interactions between Two IDPs
Biomolecules
intrinsic disordered protein
extremely fuzzy complex
protein interaction
binding mechanism
author_facet Wenning Wang
Dongdong Wang
author_sort Wenning Wang
title Extreme Fuzziness: Direct Interactions between Two IDPs
title_short Extreme Fuzziness: Direct Interactions between Two IDPs
title_full Extreme Fuzziness: Direct Interactions between Two IDPs
title_fullStr Extreme Fuzziness: Direct Interactions between Two IDPs
title_full_unstemmed Extreme Fuzziness: Direct Interactions between Two IDPs
title_sort extreme fuzziness: direct interactions between two idps
publisher MDPI AG
series Biomolecules
issn 2218-273X
publishDate 2019-02-01
description Protein interactions involving intrinsically disordered proteins (IDPs) greatly extend the range of binding mechanisms available to proteins. In interactions employing coupled folding and binding, IDPs undergo disorder-to-order transitions to form a complex with a well-defined structure. In many other cases, IDPs retain structural plasticity in the final complexes, which have been defined as the fuzzy complexes. While a large number of fuzzy complexes have been characterized with variety of fuzzy patterns, many of the interactions are between an IDP and a structured protein. Thus, whether two IDPs can interact directly to form a fuzzy complex without disorder-to-order transition remains an open question. Recently, two studies of interactions between IDPs (4.1G-CTD/NuMA and H1/ProTα) have found a definite answer to this question. Detailed characterizations combined with nuclear magnetic resonance (NMR), single-molecule Förster resonance energy transfer (smFRET) and molecular dynamics (MD) simulation demonstrate that direct interactions between these two pairs of IDPs do form fuzzy complexes while retaining the conformational dynamics of the isolated proteins, which we name as the extremely fuzzy complexes. Extreme fuzziness completes the full spectrum of protein-protein interaction modes, suggesting that a more generalized model beyond existing binding mechanisms is required. Previous models of protein interaction could be applicable to some aspects of the extremely fuzzy interactions, but in more general sense, the distinction between native and nonnative contacts, which was used to understand protein folding and binding, becomes obscure. Exploring the phenomenon of extreme fuzziness may shed new light on molecular recognition and drug design.
topic intrinsic disordered protein
extremely fuzzy complex
protein interaction
binding mechanism
url https://www.mdpi.com/2218-273X/9/3/81
work_keys_str_mv AT wenningwang extremefuzzinessdirectinteractionsbetweentwoidps
AT dongdongwang extremefuzzinessdirectinteractionsbetweentwoidps
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