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Mechanism of coupled folding and binding of an intrinsically disordered protein
by
Sugase, Kenji
, Dyson, H. Jane
, Wright, Peter E.
in
Binding
/ Binding energy
/ Binding sites
/ Biochemistry
/ CREB-Binding Protein - chemistry
/ CREB-Binding Protein - metabolism
/ Cyclic AMP Response Element-Binding Protein - chemistry
/ Cyclic AMP Response Element-Binding Protein - metabolism
/ Dispersions
/ Encounters
/ Eukaryotes
/ Folding
/ Humanities and Social Sciences
/ Kinases
/ Kinetics
/ letter
/ Magnetic Resonance Spectroscopy
/ Models, Molecular
/ Molecular biology
/ multidisciplinary
/ Physiology
/ Protein Binding
/ Protein Denaturation
/ Protein Folding
/ Protein Structure, Tertiary
/ Proteins
/ Science
/ Science (multidisciplinary)
/ Titration
/ Transcriptional Activation
2007
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Mechanism of coupled folding and binding of an intrinsically disordered protein
by
Sugase, Kenji
, Dyson, H. Jane
, Wright, Peter E.
in
Binding
/ Binding energy
/ Binding sites
/ Biochemistry
/ CREB-Binding Protein - chemistry
/ CREB-Binding Protein - metabolism
/ Cyclic AMP Response Element-Binding Protein - chemistry
/ Cyclic AMP Response Element-Binding Protein - metabolism
/ Dispersions
/ Encounters
/ Eukaryotes
/ Folding
/ Humanities and Social Sciences
/ Kinases
/ Kinetics
/ letter
/ Magnetic Resonance Spectroscopy
/ Models, Molecular
/ Molecular biology
/ multidisciplinary
/ Physiology
/ Protein Binding
/ Protein Denaturation
/ Protein Folding
/ Protein Structure, Tertiary
/ Proteins
/ Science
/ Science (multidisciplinary)
/ Titration
/ Transcriptional Activation
2007
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Do you wish to request the book?
Mechanism of coupled folding and binding of an intrinsically disordered protein
by
Sugase, Kenji
, Dyson, H. Jane
, Wright, Peter E.
in
Binding
/ Binding energy
/ Binding sites
/ Biochemistry
/ CREB-Binding Protein - chemistry
/ CREB-Binding Protein - metabolism
/ Cyclic AMP Response Element-Binding Protein - chemistry
/ Cyclic AMP Response Element-Binding Protein - metabolism
/ Dispersions
/ Encounters
/ Eukaryotes
/ Folding
/ Humanities and Social Sciences
/ Kinases
/ Kinetics
/ letter
/ Magnetic Resonance Spectroscopy
/ Models, Molecular
/ Molecular biology
/ multidisciplinary
/ Physiology
/ Protein Binding
/ Protein Denaturation
/ Protein Folding
/ Protein Structure, Tertiary
/ Proteins
/ Science
/ Science (multidisciplinary)
/ Titration
/ Transcriptional Activation
2007
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Mechanism of coupled folding and binding of an intrinsically disordered protein
Journal Article
Mechanism of coupled folding and binding of an intrinsically disordered protein
2007
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Overview
Many proteins that are important to cellular signalling are intrinsically disordered, as they only fold after binding with signalling partners. In this paper the molecular interactions governing such proteins' coupled folding and binding process, and how they differ radically from interactions between pre-folded proteins are described.
Protein folding and binding are analogous processes, in which the protein ‘searches’ for favourable intramolecular or intermolecular interactions on a funnelled energy landscape
1
,
2
. Many eukaryotic proteins are disordered under physiological conditions, and fold into ordered structures only on binding to their cellular targets
3
,
4
,
5
,
6
. The mechanism by which folding is coupled to binding is poorly understood, but it has been hypothesized on theoretical grounds that the binding kinetics may be enhanced by a ‘fly-casting’ effect, where the disordered protein binds weakly and non-specifically to its target and folds as it approaches the cognate binding site
7
. Here we show, using NMR titrations and
15
N relaxation dispersion, that the phosphorylated kinase inducible activation domain (pKID) of the transcription factor CREB forms an ensemble of transient encounter complexes on binding to the KIX domain of the CREB binding protein. The encounter complexes are stabilized primarily by non-specific hydrophobic contacts, and evolve by way of an intermediate to the fully bound state without dissociation from KIX. The carboxy-terminal helix of pKID is only partially folded in the intermediate, and becomes stabilized by intermolecular interactions formed in the final bound state. Future applications of our method will provide new understanding of the molecular mechanisms by which intrinsically disordered proteins perform their diverse biological functions.
Publisher
Nature Publishing Group UK,Nature Publishing Group
Subject
/ CREB-Binding Protein - chemistry
/ CREB-Binding Protein - metabolism
/ Cyclic AMP Response Element-Binding Protein - chemistry
/ Cyclic AMP Response Element-Binding Protein - metabolism
/ Folding
/ Humanities and Social Sciences
/ Kinases
/ Kinetics
/ letter
/ Magnetic Resonance Spectroscopy
/ Proteins
/ Science
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