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   <subfield code="a">10.1007/s00018-014-1733-x</subfield>
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   <subfield code="a">(NATIONALLICENCE)springer-10.1007/s00018-014-1733-x</subfield>
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   <subfield code="a">Proteolytic control of TGF-β co-receptor activity by BMP-1/tolloid-like proteases revealed by quantitative iTRAQ proteomics</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Frédéric Delolme, Cyril Anastasi, Lindsay Alcaraz, Valentin Mendoza, Sandrine Vadon-Le Goff, Maya Talantikite, Robin Capomaccio, Jimmy Mevaere, Laëtitia Fortin, Dominique Mazzocut, Odile Damour, Isabelle Zanella-Cléon, David Hulmes, Christopher Overall, Ulrich Valcourt, Fernando Lopez-Casillas, Catherine Moali]</subfield>
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   <subfield code="a">The metalloproteinase BMP-1 (bone morphogenetic protein-1) plays a major role in the control of extracellular matrix (ECM) assembly and growth factor activation. Most of the growth factors activated by BMP-1 are members of the TGF-β superfamily known to regulate multiple biological processes including embryonic development, wound healing, inflammation and tumor progression. In this study, we used an iTRAQ (isobaric tags for relative and absolute quantification)-based quantitative proteomic approach to reveal the release of proteolytic fragments from the cell surface or the ECM by BMP-1. Thirty-eight extracellular proteins were found in significantly higher or lower amounts in the conditioned medium of HT1080 cells overexpressing BMP-1 and thus, could be considered as candidate substrates. Strikingly, three of these new candidates (betaglycan, CD109 and neuropilin-1) were TGF-β co-receptors, also acting as antagonists when released from the cell surface, and were chosen for further substrate validation. Betaglycan and CD109 proved to be directly cleaved by BMP-1 and the corresponding cleavage sites were extensively characterized using a new mass spectrometry approach. Furthermore, we could show that the ability of betaglycan and CD109 to interact with TGF-β was altered after cleavage by BMP-1, leading to increased and prolonged SMAD2 phosphorylation in BMP-1-overexpressing cells. Betaglycan processing was also observed in primary corneal keratocytes, indicating a general and novel mechanism by which BMP-1 directly affects signaling by controlling TGF-β co-receptor activity. The proteomic data have been submitted to ProteomeXchange with the identifier PXD000786 and doi: 10.6019/PXD000786 .</subfield>
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   <subfield code="a">Springer Basel, 2014</subfield>
  </datafield>
  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">BMP-1/tolloid-like proteinases</subfield>
   <subfield code="2">nationallicence</subfield>
  </datafield>
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   <subfield code="a">Mass spectrometry</subfield>
   <subfield code="2">nationallicence</subfield>
  </datafield>
  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">Degradomics</subfield>
   <subfield code="2">nationallicence</subfield>
  </datafield>
  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">Surface plasmon resonance</subfield>
   <subfield code="2">nationallicence</subfield>
  </datafield>
  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">Zona pellucida</subfield>
   <subfield code="2">nationallicence</subfield>
  </datafield>
  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">Glycosaminoglycan</subfield>
   <subfield code="2">nationallicence</subfield>
  </datafield>
  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">BG : Betaglycan</subfield>
   <subfield code="2">nationallicence</subfield>
  </datafield>
  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">BMP : Bone Morphogenetic Protein</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">BSA : Bovine Serum Albumin</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">BTP : BMP-1/Tolloid-like Proteinase</subfield>
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   <subfield code="a">DTT : Dithiothreitol</subfield>
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   <subfield code="a">ECM : Extracellular Matrix</subfield>
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   <subfield code="a">GAG : Glycosaminoglycan</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">mTLD : Mammalian Tolloid</subfield>
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   <subfield code="a">mTLL-1 : Mammalian Tolloid-like 1</subfield>
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   <subfield code="a">SDS-PAGE : Sodium Dodecyl Sulfate Poly-Acrylamide Gel Electrophoresis</subfield>
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   <subfield code="a">ZP : Zona Pellucida</subfield>
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   <subfield code="a">Lopez-Casillas</subfield>
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   <subfield code="u">Instituto de Fisiologia Celular, Universidad Nacional Autonoma de Mexico, 04510, Mexico, Mexico</subfield>
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   <subfield code="t">Cellular and Molecular Life Sciences</subfield>
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   <subfield code="g">72/5(2015-03-01), 1009-1027</subfield>
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   <subfield code="a">BK010053</subfield>
   <subfield code="b">XK010053</subfield>
   <subfield code="c">XK010000</subfield>
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  <datafield tag="900" ind1=" " ind2="7">
   <subfield code="a">Metadata rights reserved</subfield>
   <subfield code="b">Springer special CC-BY-NC licence</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="q">72:5&lt;1009</subfield>
   <subfield code="1">2015</subfield>
   <subfield code="2">72</subfield>
   <subfield code="o">18</subfield>
  </datafield>
 </record>
</collection>
