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1000 Titel
  • Identification of function-regulating antibodies targeting the receptor protein tyrosine phosphatase sigma ectodomain
1000 Autor/in
  1. Wu, Chia-Lun |
  2. Hardy, Serge |
  3. Aubry, Isabelle |
  4. Landry, Melissa |
  5. Haggarty, Allison |
  6. Saragovi, Horacio Uri |
  7. Tremblay, Michel L. |
1000 Erscheinungsjahr 2017
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2017-05-30
1000 Erschienen in
1000 Quellenangabe
  • 12(5):e0178489
1000 Copyrightjahr
  • 2017
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1371/journal.pone.0178489 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5449173/ |
1000 Ergänzendes Material
  • http://creativecommons.org/licenses/by/4.0/ |
1000 Publikationsstatus
1000 Begutachtungsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Receptor tyrosine phosphatase sigma (RPTPσ) plays an important role in the regulation of axonal outgrowth and neural regeneration. Recent studies have identified two RPTPσ ligands, chondroitin sulfate proteoglycans (CSPGs) and heparan sulfate proteoglycans (HSPG), which can modulate RPTPσ activity by affecting its dimerization status. Here, we developed a split luciferase assay to monitor RPTPσ dimerization in living cells. Using this system, we demonstrate that heparin, an analog of heparan sulfate, induced the dimerization of RPTPσ, whereas chondroitin sulfate increased RPTPσ activity by inhibiting RPTPσ dimerization. Also, we generated several novel RPTPσ IgG monoclonal antibodies, to identify one that modulates its activity by inducing/stabilizing dimerization in living cells. Lastly, we demonstrate that this antibody promotes neurite outgrowth in SH-SY5Y cells. In summary, we demonstrated that the split luciferase RPTPσ activity assay is a novel high-throughput approach for discovering novel RPTPσ modulators that can promote axonal outgrowth and neural regeneration.
1000 Sacherschließung
lokal Phosphatases
lokal Transfection
lokal Dimerization
lokal Enzyme-linked immunoassays
lokal Immunoprecipitation
lokal Antibody therapy
lokal Luciferase assay
lokal Sulfates
1000 Fächerklassifikation (DDC)
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/uri/V3UsIENoaWEtTHVu|https://frl.publisso.de/adhoc/uri/SGFyZHksIFNlcmdl|https://frl.publisso.de/adhoc/uri/QXVicnksIElzYWJlbGxl|https://frl.publisso.de/adhoc/uri/TGFuZHJ5LCBNZWxpc3Nh|https://frl.publisso.de/adhoc/uri/SGFnZ2FydHksIEFsbGlzb24=|https://frl.publisso.de/adhoc/uri/U2FyYWdvdmksIEhvcmFjaW8gVXJp|https://frl.publisso.de/adhoc/uri/VHJlbWJsYXksIE1pY2hlbCBMLg==
1000 (Academic) Editor
1000 Label
1000 Förderer
  1. Canadian Institutes of Health Research |
  2. Israel Science Foundation |
  3. Azrieli Foundation |
1000 Fördernummer
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  2. -
  3. -
1000 Förderprogramm
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1000 Dateien
1000 Förderung
  1. 1000 joinedFunding-child
    1000 Förderer Canadian Institutes of Health Research |
    1000 Förderprogramm -
    1000 Fördernummer -
  2. 1000 joinedFunding-child
    1000 Förderer Israel Science Foundation |
    1000 Förderprogramm -
    1000 Fördernummer -
  3. 1000 joinedFunding-child
    1000 Förderer Azrieli Foundation |
    1000 Förderprogramm -
    1000 Fördernummer -
1000 Objektart article
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1000 @id frl:6453431.rdf
1000 Erstellt am 2023-08-08T11:25:52.447+0200
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1000 Zuletzt bearbeitet 2023-08-08T13:05:42.790+0200
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1000 Oai Id
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