Interaction of Plectin with Keratins 5 and 14: Dependence on Several Plectin Domains and Keratin Quaternary Structure.

Bouameur, Jamal-Eddine; Favre, Bertrand; Fontao, Lionel; Lingasamy, Prakash; Begré, Nadja; Borradori, Luca (2014). Interaction of Plectin with Keratins 5 and 14: Dependence on Several Plectin Domains and Keratin Quaternary Structure. Journal of Investigative Dermatology, 134(11), pp. 2776-2783. Nature Publishing 10.1038/jid.2014.255

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Plectin, a cytolinker of the plakin family, anchors the intermediate filament (IF) network formed by keratins 5 and 14 (K5/K14) to hemidesmosomes, junctional adhesion complexes in basal keratinocytes. Genetic alterations of these proteins cause epidermolysis bullosa simplex (EBS) characterized by disturbed cytoarchitecture and cell fragility. The mechanisms through which mutations located after the documented plectin IF-binding site, composed of the plakin-repeat domain (PRD) B5 and the linker, as well as mutations in K5 or K14, lead to EBS remain unclear. We investigated the interaction of plectin C terminus, encompassing four domains, the PRD B5, the linker, the PRD C, and the C extremity, with K5/K14 using different approaches, including a rapid and sensitive fluorescent protein-binding assay, based on enhanced green fluorescent protein-tagged proteins (FluoBACE). Our results demonstrate that all four plectin C-terminal domains contribute to its association with K5/K14 and act synergistically to ensure efficient IF binding. The plectin C terminus predominantly interacted with the K5/K14 coil 1 domain and bound more extensively to K5/K14 filaments compared with monomeric keratins or IF assembly intermediates. These findings indicate a multimodular association of plectin with K5/K14 filaments and give insights into the molecular basis of EBS associated with pathogenic mutations in plectin, K5, or K14 genes.Journal of Investigative Dermatology advance online publication, 10 July 2014; doi:10.1038/jid.2014.255.

Item Type:

Journal Article (Original Article)

Division/Institute:

04 Faculty of Medicine > Department of Dermatology, Urology, Rheumatology, Nephrology, Osteoporosis (DURN) > Clinic of Dermatology

UniBE Contributor:

Bouameur, Jamal-Eddine; Favre, Bertrand; Lingasamy, Prakash; Begré, Nadja and Borradori, Luca

Subjects:

600 Technology > 610 Medicine & health

ISSN:

0022-202X

Publisher:

Nature Publishing

Language:

English

Submitter:

Monika Schenk

Date Deposited:

16 Apr 2015 15:15

Last Modified:

19 Oct 2015 11:29

Publisher DOI:

10.1038/jid.2014.255

PubMed ID:

24940650

BORIS DOI:

10.7892/boris.59179

URI:

https://boris.unibe.ch/id/eprint/59179

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