Literature DB >> 28101868

Dystrophin and Spectrin, Two Highly Dissimilar Sisters of the Same Family.

Olivier Delalande1, Aleksander Czogalla2, Jean-François Hubert3, Aleksander Sikorski2, Elisabeth Le Rumeur3.   

Abstract

Dystrophin and Spectrin are two proteins essential for the organization of the cytoskeleton and for the stabilization of membrane cells. The comparison of these two sister proteins, and with the dystrophin homologue utrophin, enables us to emphasise that, despite a similar topology with common subdomains and a common structural basis of a three-helix coiled-coil, they show a large range of dissimilarities in terms of genetics, cell expression and higher level structural organisation. Interactions with cellular partners, including proteins and membrane phospholipids, also show both strikingly similar and very different behaviours. The differences between dystrophin and spectrin are also illustrated by the large variety of pathological anomalies emerging from the dysfunction or the absence of these proteins, showing that they are keystones in their function of providing a scaffold that sustains cell structure.

Entities:  

Keywords:  Coiled-coil fold; Dystrophin; Genetic disease; Membrane binding; Scaffolding protein; Spectrin

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Year:  2017        PMID: 28101868     DOI: 10.1007/978-3-319-49674-0_12

Source DB:  PubMed          Journal:  Subcell Biochem        ISSN: 0306-0225


  2 in total

1.  The role of spectrin in cell adhesion and cell-cell contact.

Authors:  Beata Machnicka; Renata Grochowalska; Dżamila M Bogusławska; Aleksander F Sikorski
Journal:  Exp Biol Med (Maywood)       Date:  2019-06-21

2.  Fine mapping of hydrophobic contacts reassesses the organization of the first three dystrophin coiled-coil repeats.

Authors:  Dominique Mias-Lucquin; Angélique Chéron; Elisabeth Le Rumeur; Jean-François Hubert; Olivier Delalande
Journal:  Protein Sci       Date:  2019-01-14       Impact factor: 6.725

  2 in total

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