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Title: Structural Basis for Interactions Between Contactin Family Members and Protein-tyrosine Phosphatase Receptor Type G in Neural Tissues

Protein-tyrosine phosphatase receptor type G (RPTPγ/PTPRG) interacts in vitro with contactin-3-6 (CNTN3-6), a group of glycophosphatidylinositol-anchored cell adhesion molecules involved in the wiring of the nervous system. In addition to PTPRG, CNTNs associate with multiple transmembrane proteins and signal inside the cell via cis-binding partners to alleviate the absence of an intracellular region. Here, we use comprehensive biochemical and structural analyses to demonstrate that PTPRG·CNTN3-6 complexes share similar binding affinities and a conserved arrangement. Furthermore, as a first step to identifying PTPRG·CNTN complexes in vivo, we found that PTPRG and CNTN3 associate in the outer segments of mouse rod photoreceptor cells. In particular, PTPRG and CNTN3 form cis-complexes at the surface of photoreceptors yet interact in trans when expressed on the surfaces of apposing cells. Further structural analyses suggest that all CNTN ectodomains adopt a bent conformation and might lie parallel to the cell surface to accommodate these cis and trans binding modes. Taken together, these studies identify a PTPRG·CNTN complex in vivo and provide novel insights into PTPRG- and CNTN-mediated signaling.
Authors:
 [1] ;  [2] ;  [3] ;  [1] ;  [1] ;  [1] ;  [1] ;  [4] ;  [5] ;  [1]
  1. Univ. of Missouri, Kansas City, MO (United States)
  2. Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States)
  3. Inst. Pasteur de Paris (France); Univ. Paris Diderot (France)
  4. Univ. Paris Diderot (France)
  5. Univ. of Missouri, Kansas City, MO (United States). School of Medicine
Publication Date:
Grant/Contract Number:
AC02-05CH11231
Type:
Accepted Manuscript
Journal Name:
Journal of Biological Chemistry
Additional Journal Information:
Journal Volume: 291; Journal Issue: 41; Journal ID: ISSN 0021-9258
Publisher:
American Society for Biochemistry and Molecular Biology
Research Org:
Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States)
Sponsoring Org:
USDOE Office of Science (SC), Basic Energy Sciences (BES) (SC-22)
Country of Publication:
United States
Language:
English
Subject:
59 BASIC BIOLOGICAL SCIENCES
OSTI Identifier:
1408402

Nikolaienko, Roman M., Hammel, Michal, Dubreuil, Véronique, Zalmai, Rana, Hall, David R., Mehzabeen, Nurjahan, Karuppan, Sebastian J., Harroch, Sheila, Stella, Salvatore L., and Bouyain, Samuel. Structural Basis for Interactions Between Contactin Family Members and Protein-tyrosine Phosphatase Receptor Type G in Neural Tissues. United States: N. p., Web. doi:10.1074/jbc.M116.742163.
Nikolaienko, Roman M., Hammel, Michal, Dubreuil, Véronique, Zalmai, Rana, Hall, David R., Mehzabeen, Nurjahan, Karuppan, Sebastian J., Harroch, Sheila, Stella, Salvatore L., & Bouyain, Samuel. Structural Basis for Interactions Between Contactin Family Members and Protein-tyrosine Phosphatase Receptor Type G in Neural Tissues. United States. doi:10.1074/jbc.M116.742163.
Nikolaienko, Roman M., Hammel, Michal, Dubreuil, Véronique, Zalmai, Rana, Hall, David R., Mehzabeen, Nurjahan, Karuppan, Sebastian J., Harroch, Sheila, Stella, Salvatore L., and Bouyain, Samuel. 2016. "Structural Basis for Interactions Between Contactin Family Members and Protein-tyrosine Phosphatase Receptor Type G in Neural Tissues". United States. doi:10.1074/jbc.M116.742163. https://www.osti.gov/servlets/purl/1408402.
@article{osti_1408402,
title = {Structural Basis for Interactions Between Contactin Family Members and Protein-tyrosine Phosphatase Receptor Type G in Neural Tissues},
author = {Nikolaienko, Roman M. and Hammel, Michal and Dubreuil, Véronique and Zalmai, Rana and Hall, David R. and Mehzabeen, Nurjahan and Karuppan, Sebastian J. and Harroch, Sheila and Stella, Salvatore L. and Bouyain, Samuel},
abstractNote = {Protein-tyrosine phosphatase receptor type G (RPTPγ/PTPRG) interacts in vitro with contactin-3-6 (CNTN3-6), a group of glycophosphatidylinositol-anchored cell adhesion molecules involved in the wiring of the nervous system. In addition to PTPRG, CNTNs associate with multiple transmembrane proteins and signal inside the cell via cis-binding partners to alleviate the absence of an intracellular region. Here, we use comprehensive biochemical and structural analyses to demonstrate that PTPRG·CNTN3-6 complexes share similar binding affinities and a conserved arrangement. Furthermore, as a first step to identifying PTPRG·CNTN complexes in vivo, we found that PTPRG and CNTN3 associate in the outer segments of mouse rod photoreceptor cells. In particular, PTPRG and CNTN3 form cis-complexes at the surface of photoreceptors yet interact in trans when expressed on the surfaces of apposing cells. Further structural analyses suggest that all CNTN ectodomains adopt a bent conformation and might lie parallel to the cell surface to accommodate these cis and trans binding modes. Taken together, these studies identify a PTPRG·CNTN complex in vivo and provide novel insights into PTPRG- and CNTN-mediated signaling.},
doi = {10.1074/jbc.M116.742163},
journal = {Journal of Biological Chemistry},
number = 41,
volume = 291,
place = {United States},
year = {2016},
month = {8}
}

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