Literature DB >> 30066087

Intrinsically disordered proteins in crowded milieu: when chaos prevails within the cellular gumbo.

Alexander V Fonin1, April L Darling2, Irina M Kuznetsova1, Konstantin K Turoverov1,3, Vladimir N Uversky4.   

Abstract

Effects of macromolecular crowding on structural and functional properties of ordered proteins, their folding, interactability, and aggregation are well documented. Much less is known about how macromolecular crowding might affect structural and functional behaviour of intrinsically disordered proteins (IDPs) or intrinsically disordered protein regions (IDPRs). To fill this gap, this review represents a systematic analysis of the available literature data on the behaviour of IDPs/IDPRs in crowded environment. Although it was hypothesized that, due to the excluded-volume effects present in crowded environments, IDPs/IDPRs would invariantly fold in the presence of high concentrations of crowding agents or in the crowded cellular environment, accumulated data indicate that, based on their response to the presence of crowders, IDPs/IDPRs can be grouped into three major categories, foldable, non-foldable, and unfoldable. This is because natural cellular environment is not simply characterized by the presence of high concentration of "inert" macromolecules, but represents an active milieu, components of which are engaged in direct physical interactions and soft interactions with target proteins. Some of these interactions with cellular components can cause (local) unfolding of query proteins. In other words, since crowding can cause both folding and unfolding of an IDP or its regions, the outputs of the placing of a query protein to the crowded environment would depend on the balance between these two processes. As a result, and because of the spatio-temporal heterogeneity in structural organization of IDPs, macromolecular crowding can differently affect structures of different IDPs. Recent studies indicate that some IDPs are able to undergo liquid-liquid-phase transitions leading to the formation of various proteinaceous membrane-less organelles (PMLOs). Although interiors of such PMLOs are self-crowded, being characterized by locally increased concentrations of phase-separating IDPs, these IDPs are minimally foldable or even non-foldable at all (at least within the physiologically safe time-frame of normal PMLO existence).

Entities:  

Keywords:  Conformational stability; Induced folding; Intrinsically disordered protein; Intrinsically disordered protein region; Macromolecular crowding; Proteinaceous membrane-less organelles

Mesh:

Substances:

Year:  2018        PMID: 30066087     DOI: 10.1007/s00018-018-2894-9

Source DB:  PubMed          Journal:  Cell Mol Life Sci        ISSN: 1420-682X            Impact factor:   9.261


  244 in total

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Journal:  Curr Biol       Date:  2000-02-10       Impact factor: 10.834

2.  Effects of macromolecular crowding on the intrinsically disordered proteins c-Fos and p27(Kip1).

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Journal:  Biomacromolecules       Date:  2001       Impact factor: 6.988

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4.  Effect of dextran on protein stability and conformation attributed to macromolecular crowding.

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Journal:  J Mol Biol       Date:  2003-02-28       Impact factor: 5.469

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Journal:  Cell       Date:  1997-10-17       Impact factor: 41.582

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Authors:  Jia Bai; Maili Liu; Gary J Pielak; Conggang Li
Journal:  Chemphyschem       Date:  2016-12-02       Impact factor: 3.102

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7.  Determining the Protective Activity of IDPs Under Partial Dehydration and Freeze-Thaw Conditions.

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Journal:  Methods Mol Biol       Date:  2020

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9.  Crowding Effects on the Structure and Dynamics of the Intrinsically Disordered Nuclear Chromatin Protein NUPR1.

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10.  Determination of the molecular reach of the protein tyrosine phosphatase SHP-1.

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