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Structural basis of semaphorin-plexin cis interaction.
Rozbesky, Daniel; Verhagen, Marieke G; Karia, Dimple; Nagy, Gergely N; Alvarez, Luis; Robinson, Ross A; Harlos, Karl; Padilla-Parra, Sergi; Pasterkamp, R Jeroen; Jones, Edith Yvonne.
Afiliação
  • Rozbesky D; Division of Structural Biology, Wellcome Centre for Human Genetics, University of Oxford, Oxford, UK.
  • Verhagen MG; Department of Translational Neuroscience, UMC Utrecht Brain Center, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.
  • Karia D; Division of Structural Biology, Wellcome Centre for Human Genetics, University of Oxford, Oxford, UK.
  • Nagy GN; Division of Structural Biology, Wellcome Centre for Human Genetics, University of Oxford, Oxford, UK.
  • Alvarez L; Cellular Imaging, Wellcome Centre for Human Genetics, University of Oxford, Oxford, UK.
  • Robinson RA; Division of Structural Biology, Wellcome Centre for Human Genetics, University of Oxford, Oxford, UK.
  • Harlos K; Division of Structural Biology, Wellcome Centre for Human Genetics, University of Oxford, Oxford, UK.
  • Padilla-Parra S; Division of Structural Biology, Wellcome Centre for Human Genetics, University of Oxford, Oxford, UK.
  • Pasterkamp RJ; Cellular Imaging, Wellcome Centre for Human Genetics, University of Oxford, Oxford, UK.
  • Jones EY; Department of Translational Neuroscience, UMC Utrecht Brain Center, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.
EMBO J ; 39(13): e102926, 2020 07 01.
Article em En | MEDLINE | ID: mdl-32500924
Semaphorin ligands interact with plexin receptors to contribute to functions in the development of myriad tissues including neurite guidance and synaptic organisation within the nervous system. Cell-attached semaphorins interact in trans with plexins on opposing cells, but also in cis on the same cell. The interplay between trans and cis interactions is crucial for the regulated development of complex neural circuitry, but the underlying molecular mechanisms are uncharacterised. We have discovered a distinct mode of interaction through which the Drosophila semaphorin Sema1b and mouse Sema6A mediate binding in cis to their cognate plexin receptors. Our high-resolution structural, biophysical and in vitro analyses demonstrate that monomeric semaphorins can mediate a distinctive plexin binding mode. These findings suggest the interplay between monomeric vs dimeric states has a hereto unappreciated role in semaphorin biology, providing a mechanism by which Sema6s may balance cis and trans functionalities.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Moléculas de Adesão Celular / Proteínas de Drosophila / Semaforinas / Proteínas do Tecido Nervoso Limite: Animals Idioma: En Revista: EMBO J Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Moléculas de Adesão Celular / Proteínas de Drosophila / Semaforinas / Proteínas do Tecido Nervoso Limite: Animals Idioma: En Revista: EMBO J Ano de publicação: 2020 Tipo de documento: Article