Fernanda Mello de Queiroz

Max Planck Institute for Experimental Medicine, Göttingen, Lower Saxony, Germany

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Publications (1)5.43 Total impact

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    ABSTRACT: Focal adhesion kinase (FAK) controls cellular adhesion and motility processes by its tight link to integrin- and extracellular-matrix-mediated signaling. To explore the dynamics of the regulation of FAK, we constructed a FRET-based probe that visualizes conformational rearrangements of the FERM domain of FAK in living cells. The sensor reports on an integrin-mediated conformational change in FAK following cellular adhesion. The perturbation is kinase-independent and involves the polybasic KAKTLR sequence in the FERM domain. It is manifested by an increased FRET signal and is expressed primarily in focal adhesions, and to a lesser extent in the cytoplasm. The conformational change in the FERM domain of FAK is observed in two consecutive phases during spreading - early and late - and is enriched in fully adhered motile cells at growing and sliding peripheral focal-adhesion sites, but not in stable or retracting focal adhesions. Inhibition of the actomyosin system indicates the involvement of tension signaling induced by Rho-associated kinase, rather than by myosin light-chain kinase, in the modulation of the FERM response. We conclude that the heterogeneous conformation of the FERM domain in focal adhesions of migrating cells reflects a complex regulatory mechanism for FAK that appears to be under the influence of cellular traction forces.
    Journal of Cell Science 03/2009; 122(Pt 5):656-66. DOI:10.1242/jcs.028738 · 5.43 Impact Factor

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31 Citations
5.43 Total Impact Points

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  • 2009
    • Max Planck Institute for Experimental Medicine
      Göttingen, Lower Saxony, Germany