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    How pathogens use linear motifs to perturb host cell networks

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    Type
    Article
    Authors
    Via, Allegra
    Uyar, Bora
    Brun, Christine
    Zanzoni, Andreas
    KAUST Grant Number
    KUK-I1-012-43
    Date
    2015-01
    Permanent link to this record
    http://hdl.handle.net/10754/598519
    
    Metadata
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    Abstract
    Molecular 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.
    Citation
    Via 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.
    Sponsors
    The 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).
    Publisher
    Elsevier BV
    Journal
    Trends in Biochemical Sciences
    DOI
    10.1016/j.tibs.2014.11.001
    PubMed ID
    25475989
    ae974a485f413a2113503eed53cd6c53
    10.1016/j.tibs.2014.11.001
    Scopus Count
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