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Development and characterization of functional antibodies targeting NMDA receptors
N-methyl-D-aspartate receptors (NMDARs) are critically involved in basic brain functions and neurodegeneration as well as tumor invasiveness. Targeting specific subtypes of NMDARs with distinct activities has been considered an effective therapeutic strategy for neurological disorders and diseases....
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8854693/ https://www.ncbi.nlm.nih.gov/pubmed/35177668 http://dx.doi.org/10.1038/s41467-022-28559-3 |
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author | Tajima, Nami Simorowski, Noriko Yovanno, Remy A. Regan, Michael C. Michalski, Kevin Gómez, Ricardo Lau, Albert Y. Furukawa, Hiro |
author_facet | Tajima, Nami Simorowski, Noriko Yovanno, Remy A. Regan, Michael C. Michalski, Kevin Gómez, Ricardo Lau, Albert Y. Furukawa, Hiro |
author_sort | Tajima, Nami |
collection | PubMed |
description | N-methyl-D-aspartate receptors (NMDARs) are critically involved in basic brain functions and neurodegeneration as well as tumor invasiveness. Targeting specific subtypes of NMDARs with distinct activities has been considered an effective therapeutic strategy for neurological disorders and diseases. However, complete elimination of off-target effects of small chemical compounds has been challenging and thus, there is a need to explore alternative strategies for targeting NMDAR subtypes. Here we report identification of a functional antibody that specifically targets the GluN1-GluN2B NMDAR subtype and allosterically down-regulates ion channel activity as assessed by electrophysiology. Through biochemical analysis, x-ray crystallography, single-particle electron cryomicroscopy, and molecular dynamics simulations, we show that this inhibitory antibody recognizes the amino terminal domain of the GluN2B subunit and increases the population of the non-active conformational state. The current study demonstrates that antibodies may serve as specific reagents to regulate NMDAR functions for basic research and therapeutic objectives. |
format | Online Article Text |
id | pubmed-8854693 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-88546932022-03-04 Development and characterization of functional antibodies targeting NMDA receptors Tajima, Nami Simorowski, Noriko Yovanno, Remy A. Regan, Michael C. Michalski, Kevin Gómez, Ricardo Lau, Albert Y. Furukawa, Hiro Nat Commun Article N-methyl-D-aspartate receptors (NMDARs) are critically involved in basic brain functions and neurodegeneration as well as tumor invasiveness. Targeting specific subtypes of NMDARs with distinct activities has been considered an effective therapeutic strategy for neurological disorders and diseases. However, complete elimination of off-target effects of small chemical compounds has been challenging and thus, there is a need to explore alternative strategies for targeting NMDAR subtypes. Here we report identification of a functional antibody that specifically targets the GluN1-GluN2B NMDAR subtype and allosterically down-regulates ion channel activity as assessed by electrophysiology. Through biochemical analysis, x-ray crystallography, single-particle electron cryomicroscopy, and molecular dynamics simulations, we show that this inhibitory antibody recognizes the amino terminal domain of the GluN2B subunit and increases the population of the non-active conformational state. The current study demonstrates that antibodies may serve as specific reagents to regulate NMDAR functions for basic research and therapeutic objectives. Nature Publishing Group UK 2022-02-17 /pmc/articles/PMC8854693/ /pubmed/35177668 http://dx.doi.org/10.1038/s41467-022-28559-3 Text en © The Author(s) 2022 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Tajima, Nami Simorowski, Noriko Yovanno, Remy A. Regan, Michael C. Michalski, Kevin Gómez, Ricardo Lau, Albert Y. Furukawa, Hiro Development and characterization of functional antibodies targeting NMDA receptors |
title | Development and characterization of functional antibodies targeting NMDA receptors |
title_full | Development and characterization of functional antibodies targeting NMDA receptors |
title_fullStr | Development and characterization of functional antibodies targeting NMDA receptors |
title_full_unstemmed | Development and characterization of functional antibodies targeting NMDA receptors |
title_short | Development and characterization of functional antibodies targeting NMDA receptors |
title_sort | development and characterization of functional antibodies targeting nmda receptors |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8854693/ https://www.ncbi.nlm.nih.gov/pubmed/35177668 http://dx.doi.org/10.1038/s41467-022-28559-3 |
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