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dc.contributor.authorVia, Allegra
dc.contributor.authorUyar, Bora
dc.contributor.authorBrun, Christine
dc.contributor.authorZanzoni, Andreas
dc.date.accessioned2016-02-25T13:31:27Z
dc.date.available2016-02-25T13:31:27Z
dc.date.issued2015-01
dc.identifier.citationVia A, Uyar B, Brun C, Zanzoni A (2015) How pathogens use linear motifs to perturb host cell networks. Trends in Biochemical Sciences 40: 36–48. Available: http://dx.doi.org/10.1016/j.tibs.2014.11.001.
dc.identifier.issn0968-0004
dc.identifier.pmid25475989
dc.identifier.doi10.1016/j.tibs.2014.11.001
dc.identifier.urihttp://hdl.handle.net/10754/598519
dc.description.abstractMolecular mimicry is one of the powerful stratagems that pathogens employ to colonise their hosts and take advantage of host cell functions to guarantee their replication and dissemination. In particular, several viruses have evolved the ability to interact with host cell components through protein short linear motifs (SLiMs) that mimic host SLiMs, thus facilitating their internalisation and the manipulation of a wide range of cellular networks. Here we present convincing evidence from the literature that motif mimicry also represents an effective, widespread hijacking strategy in prokaryotic and eukaryotic parasites. Further insights into host motif mimicry would be of great help in the elucidation of the molecular mechanisms behind host cell invasion and the development of anti-infective therapeutic strategies.
dc.description.sponsorshipThe authors are grateful to David G. Biron (CNRS, France), Toby J. Gibson (EMBL, Germany), and Vincenzo Petrarca (Sapienza University, Italy) for critically reading the manuscript and providing fruitful suggestions. A.V. acknowledges the King Abdullah University of Science and Technology (KAUST) Award No. KUK-I1-012-43 for funding support. C.B. and A.Z. received financial support from the French 'Plan Cancer 2009-2013' (Systems Biology call, A12171AS).
dc.publisherElsevier BV
dc.titleHow pathogens use linear motifs to perturb host cell networks
dc.typeArticle
dc.identifier.journalTrends in Biochemical Sciences
dc.contributor.institutionDepartment of Physics, Sapienza University, 00185 Rome, Italy
dc.contributor.institutionStructural and Computational Biology, European Molecular Biology Laboratory, 69117 Heidelberg, Germany
dc.contributor.institutionInserm, UMR1090 TAGC, Marseille F-13288, France
dc.contributor.institutionAix-Marseille Université, UMR1090 TAGC, Marseille F-13288, France
dc.contributor.institutionCNRS, Marseille F-13402, France
kaust.grant.numberKUK-I1-012-43


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