Literature DB >> 34033898

Desmosomal protein structure and function and the impact of disease-causing mutations.

Fiyaz Mohammed1, Martyn Chidgey2.   

Abstract

In this graphical review we focus on the structural characteristics of desmosomal proteins, their interactions with each other and with the intermediate filament cytoskeleton. The wealth of structural information that is now available allows predictions to be made about the pathogenic effect of disease-causing mutations. We have selected representative examples of missense mutations that are buried, semi-buried or surface exposed, and demonstrate how such variants could affect the structural fold of desmosomal proteins that are expressed in the heart. We explain how such alterations could compromise desmosomal adhesion, resulting in life threatening diseases including arrhythmogenic right ventricular cardiomyopathy.
Copyright © 2021 The Author(s). Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Arrhythmogenic right ventricular cardiomyopathy; Cell–cell adhesion; Desmosomal proteins; Desmosome; Disease-related missense mutations

Mesh:

Substances:

Year:  2021        PMID: 34033898     DOI: 10.1016/j.jsb.2021.107749

Source DB:  PubMed          Journal:  J Struct Biol        ISSN: 1047-8477            Impact factor:   2.867


  2 in total

1.  Missense Mutations in Desmoplakin Plakin Repeat Domains Have Dramatic Effects on Domain Structure and Function.

Authors:  Fiyaz Mohammed; Elena Odintsova; Martyn Chidgey
Journal:  Int J Mol Sci       Date:  2022-01-04       Impact factor: 5.923

2.  Cortical tension regulates desmosomal morphogenesis.

Authors:  Marcin Moch; Jana Schieren; Rudolf E Leube
Journal:  Front Cell Dev Biol       Date:  2022-10-04
  2 in total

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