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Antibody-directed extracellular proximity biotinylation reveals that Contactin-1 regulates axo-axonic innervation of axon initial segments

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 use antibody-directed proximity biotinylation to define the cell...

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Autores principales: Ogawa, Yuki, Lim, Brian C., George, Shanu, Oses-Prieto, Juan A., Rasband, Joshua M., Eshed-Eisenbach, Yael, Hamdan, Hamdan, Nair, Supna, Boato, Francesco, Peles, Elior, Burlingame, Alma L., Van Aelst, Linda, Rasband, Matthew N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10603070/
https://www.ncbi.nlm.nih.gov/pubmed/37884508
http://dx.doi.org/10.1038/s41467-023-42273-8
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author Ogawa, Yuki
Lim, Brian C.
George, Shanu
Oses-Prieto, Juan A.
Rasband, Joshua M.
Eshed-Eisenbach, Yael
Hamdan, Hamdan
Nair, Supna
Boato, Francesco
Peles, Elior
Burlingame, Alma L.
Van Aelst, Linda
Rasband, Matthew N.
author_facet Ogawa, Yuki
Lim, Brian C.
George, Shanu
Oses-Prieto, Juan A.
Rasband, Joshua M.
Eshed-Eisenbach, Yael
Hamdan, Hamdan
Nair, Supna
Boato, Francesco
Peles, Elior
Burlingame, Alma L.
Van Aelst, Linda
Rasband, Matthew N.
author_sort Ogawa, Yuki
collection PubMed
description 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 use 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 use CRISPR-mediated genome editing for insertion of epitope tags in the endogenous proteins. We identify Contactin-1 (Cntn1) as an AIS cell surface protein. 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 regulates AIS axo-axonic innervation by inhibitory basket cells in the cerebellum and inhibitory chandelier cells in the cortex.
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spelling pubmed-106030702023-10-28 Antibody-directed extracellular proximity biotinylation reveals that 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 Hamdan, Hamdan Nair, Supna Boato, Francesco Peles, Elior Burlingame, Alma L. Van Aelst, Linda Rasband, Matthew N. Nat Commun Article 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 use 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 use CRISPR-mediated genome editing for insertion of epitope tags in the endogenous proteins. We identify Contactin-1 (Cntn1) as an AIS cell surface protein. 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 regulates AIS axo-axonic innervation by inhibitory basket cells in the cerebellum and inhibitory chandelier cells in the cortex. Nature Publishing Group UK 2023-10-26 /pmc/articles/PMC10603070/ /pubmed/37884508 http://dx.doi.org/10.1038/s41467-023-42273-8 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Ogawa, Yuki
Lim, Brian C.
George, Shanu
Oses-Prieto, Juan A.
Rasband, Joshua M.
Eshed-Eisenbach, Yael
Hamdan, Hamdan
Nair, Supna
Boato, Francesco
Peles, Elior
Burlingame, Alma L.
Van Aelst, Linda
Rasband, Matthew N.
Antibody-directed extracellular proximity biotinylation reveals that Contactin-1 regulates axo-axonic innervation of axon initial segments
title Antibody-directed extracellular proximity biotinylation reveals that Contactin-1 regulates axo-axonic innervation of axon initial segments
title_full Antibody-directed extracellular proximity biotinylation reveals that Contactin-1 regulates axo-axonic innervation of axon initial segments
title_fullStr Antibody-directed extracellular proximity biotinylation reveals that Contactin-1 regulates axo-axonic innervation of axon initial segments
title_full_unstemmed Antibody-directed extracellular proximity biotinylation reveals that Contactin-1 regulates axo-axonic innervation of axon initial segments
title_short Antibody-directed extracellular proximity biotinylation reveals that Contactin-1 regulates axo-axonic innervation of axon initial segments
title_sort antibody-directed extracellular proximity biotinylation reveals that contactin-1 regulates axo-axonic innervation of axon initial segments
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10603070/
https://www.ncbi.nlm.nih.gov/pubmed/37884508
http://dx.doi.org/10.1038/s41467-023-42273-8
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