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Antibody-directed extracellular proximity biotinylation reveals Contactin-1 regulates axo-axonic innervation of axon initial segments.
Ogawa, Yuki; Lim, Brian C; George, Shanu; Oses-Prieto, Juan A; Rasband, Joshua M; Eshed-Eisenbach, Yael; Nair, Supna; Boato, Francesco; Peles, Elior; Burlingame, Alma L; Van Aelst, Linda; Rasband, Matthew N.
Affiliation
  • Ogawa Y; Baylor College of Medicine, Department of Neuroscience, Houston, TX, USA.
  • Lim BC; Baylor College of Medicine, Department of Neuroscience, Houston, TX, USA.
  • George S; Cold Spring Harbor Laboratory, Division of Neuroscience, Cold Spring Harbor, NY, USA.
  • Oses-Prieto JA; University of California San Francisco, Department of Pharmaceutical Chemistry, San Francisco, CA, USA.
  • Rasband JM; Baylor College of Medicine, Department of Neuroscience, Houston, TX, USA.
  • Eshed-Eisenbach Y; Weizmann Institute of Science, Department of Molecular Cell Biology, Rehovot, Israel.
  • Nair S; University of California San Francisco, Department of Pharmaceutical Chemistry, San Francisco, CA, USA.
  • Boato F; Cold Spring Harbor Laboratory, Division of Neuroscience, Cold Spring Harbor, NY, USA.
  • Peles E; Weizmann Institute of Science, Department of Molecular Cell Biology, Rehovot, Israel.
  • Burlingame AL; University of California San Francisco, Department of Pharmaceutical Chemistry, San Francisco, CA, USA.
  • Van Aelst L; Cold Spring Harbor Laboratory, Division of Neuroscience, Cold Spring Harbor, NY, USA.
  • Rasband MN; Baylor College of Medicine, Department of Neuroscience, Houston, TX, USA.
bioRxiv ; 2023 Mar 06.
Article in En | MEDLINE | ID: mdl-36945454
ABSTRACT
Axon initial segment (AIS) cell surface proteins mediate key biological processes in neurons including action potential initiation and axo-axonic synapse formation. However, few AIS cell surface proteins have been identified. Here, we used antibody-directed proximity biotinylation to define the cell surface proteins in close proximity to the AIS cell adhesion molecule Neurofascin. To determine the distributions of the identified proteins, we used CRISPR-mediated genome editing for insertion of epitope tags in the endogenous proteins. We found Contactin-1 (Cntn1) among the previously unknown AIS proteins we identified. Cntn1 is enriched at the AIS through interactions with Neurofascin and NrCAM. We further show that Cntn1 contributes to assembly of the AIS-extracellular matrix, and is required for AIS axo-axonic innervation by inhibitory basket cells in the cerebellum and inhibitory chandelier cells in the cortex.

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: BioRxiv Year: 2023 Document type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: BioRxiv Year: 2023 Document type: Article Affiliation country: United States