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Desmoplakin CSM models unravel mechanisms regulating the binding to intermediate filaments and putative therapeutics for cardiocutaneous diseases
by
Badowski, Cedric
, Benny, Paula
, Lane, E. Birgitte
, Verma, Chandra S.
in
631/154/1435/2418
/ 631/80/128/1580
/ 631/80/79/1416
/ Arginine methylation
/ Arrhythmogenic cardiomyopathy
/ Arrhythmogenic Right Ventricular Dysplasia - genetics
/ Arrhythmogenic Right Ventricular Dysplasia - metabolism
/ Cardiomyopathy
/ Coronary artery disease
/ Desmin intermediate filaments
/ Desmoplakin carboxyterminal tail
/ Desmoplakins - genetics
/ Desmoplakins - metabolism
/ Desmosomes
/ Drug development
/ Filaments
/ Heart diseases
/ Humanities and Social Sciences
/ Humans
/ Intermediate filaments
/ Intermediate Filaments - metabolism
/ Models, Molecular
/ multidisciplinary
/ Mutation
/ Post-translation
/ Protein Binding
/ Protein Processing, Post-Translational
/ Science
/ Science (multidisciplinary)
/ Serine phosphorylation
/ Young adults
2024
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Desmoplakin CSM models unravel mechanisms regulating the binding to intermediate filaments and putative therapeutics for cardiocutaneous diseases
by
Badowski, Cedric
, Benny, Paula
, Lane, E. Birgitte
, Verma, Chandra S.
in
631/154/1435/2418
/ 631/80/128/1580
/ 631/80/79/1416
/ Arginine methylation
/ Arrhythmogenic cardiomyopathy
/ Arrhythmogenic Right Ventricular Dysplasia - genetics
/ Arrhythmogenic Right Ventricular Dysplasia - metabolism
/ Cardiomyopathy
/ Coronary artery disease
/ Desmin intermediate filaments
/ Desmoplakin carboxyterminal tail
/ Desmoplakins - genetics
/ Desmoplakins - metabolism
/ Desmosomes
/ Drug development
/ Filaments
/ Heart diseases
/ Humanities and Social Sciences
/ Humans
/ Intermediate filaments
/ Intermediate Filaments - metabolism
/ Models, Molecular
/ multidisciplinary
/ Mutation
/ Post-translation
/ Protein Binding
/ Protein Processing, Post-Translational
/ Science
/ Science (multidisciplinary)
/ Serine phosphorylation
/ Young adults
2024
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Desmoplakin CSM models unravel mechanisms regulating the binding to intermediate filaments and putative therapeutics for cardiocutaneous diseases
by
Badowski, Cedric
, Benny, Paula
, Lane, E. Birgitte
, Verma, Chandra S.
in
631/154/1435/2418
/ 631/80/128/1580
/ 631/80/79/1416
/ Arginine methylation
/ Arrhythmogenic cardiomyopathy
/ Arrhythmogenic Right Ventricular Dysplasia - genetics
/ Arrhythmogenic Right Ventricular Dysplasia - metabolism
/ Cardiomyopathy
/ Coronary artery disease
/ Desmin intermediate filaments
/ Desmoplakin carboxyterminal tail
/ Desmoplakins - genetics
/ Desmoplakins - metabolism
/ Desmosomes
/ Drug development
/ Filaments
/ Heart diseases
/ Humanities and Social Sciences
/ Humans
/ Intermediate filaments
/ Intermediate Filaments - metabolism
/ Models, Molecular
/ multidisciplinary
/ Mutation
/ Post-translation
/ Protein Binding
/ Protein Processing, Post-Translational
/ Science
/ Science (multidisciplinary)
/ Serine phosphorylation
/ Young adults
2024
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Desmoplakin CSM models unravel mechanisms regulating the binding to intermediate filaments and putative therapeutics for cardiocutaneous diseases
Journal Article
Desmoplakin CSM models unravel mechanisms regulating the binding to intermediate filaments and putative therapeutics for cardiocutaneous diseases
2024
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Overview
Arrhythmogenic cardiomyopathy (AC) is a common cause of sudden cardiac arrest and death in young adults. It can be induced by different types of mutations throughout the desmoplakin gene including the R2834H mutation in the extreme carboxyterminus tail of desmoplakin (DP CT) which remains structurally uncharacterized and poorly understood. Here, we have created 3D models of DP CT which show the structural effects of AC-inducing mutations as well as the implications of post-translational modifications (PTMs). Our results suggest that, in absence of PTMs, positively charged wildtype DP CT likely folds back onto negatively-charged plectin repeat 14 of nearby plakin repeat domain C (PRD C) contributing to the recruitment of intermediate filaments (IFs). When phosphorylated and methylated, negatively-charged wildtype DP CT would then fold back onto positively-charged plectin repeat 17 of PRD C, promoting the repulsion of intermediate filaments. However, by preventing PTMs, the R2834H mutation would lead to the formation of a cytoplasmic mutant desmoplakin with a constitutively positive DP CT tail that would be aberrantly recruited by cytoplasmic IFs instead of desmosomes, potentially weakening cell-cell contacts and promoting AC. Virtual screening of FDA-approved drug libraries identified several promising drug candidates for the treatment of cardiocutaneous diseases through drug repurposing.
Publisher
Nature Publishing Group UK,Nature Publishing Group,Nature Portfolio
Subject
/ Arrhythmogenic cardiomyopathy
/ Arrhythmogenic Right Ventricular Dysplasia - genetics
/ Arrhythmogenic Right Ventricular Dysplasia - metabolism
/ Desmin intermediate filaments
/ Desmoplakin carboxyterminal tail
/ Humanities and Social Sciences
/ Humans
/ Intermediate Filaments - metabolism
/ Mutation
/ Protein Processing, Post-Translational
/ Science
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