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Stitching the synapse: Cross-linking mass spectrometry into resolving synaptic protein interactions
Synaptic transmission is the predominant form of communication in the brain. It requires functionally specialized molecular machineries constituted by thousands of interacting synaptic proteins. Here, we made use of recent advances in cross-linking mass spectrometry (XL-MS) in combination with bioch...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7030922/ https://www.ncbi.nlm.nih.gov/pubmed/32128395 http://dx.doi.org/10.1126/sciadv.aax5783 |
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author | Gonzalez-Lozano, M. A. Koopmans, F. Sullivan, P. F. Protze, J. Krause, G. Verhage, M. Li, K. W. Liu, F. Smit, A. B. |
author_facet | Gonzalez-Lozano, M. A. Koopmans, F. Sullivan, P. F. Protze, J. Krause, G. Verhage, M. Li, K. W. Liu, F. Smit, A. B. |
author_sort | Gonzalez-Lozano, M. A. |
collection | PubMed |
description | Synaptic transmission is the predominant form of communication in the brain. It requires functionally specialized molecular machineries constituted by thousands of interacting synaptic proteins. Here, we made use of recent advances in cross-linking mass spectrometry (XL-MS) in combination with biochemical and computational approaches to reveal the architecture and assembly of synaptic protein complexes from mouse brain hippocampus and cerebellum. We obtained 11,999 unique lysine-lysine cross-links, comprising connections within and between 2362 proteins. This extensive collection was the basis to identify novel protein partners, to model protein conformational dynamics, and to delineate within and between protein interactions of main synaptic constituents, such as Camk2, the AMPA-type glutamate receptor, and associated proteins. Using XL-MS, we generated a protein interaction resource that we made easily accessible via a web-based platform (http://xlink.cncr.nl) to provide new entries into exploration of all protein interactions identified. |
format | Online Article Text |
id | pubmed-7030922 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-70309222020-03-03 Stitching the synapse: Cross-linking mass spectrometry into resolving synaptic protein interactions Gonzalez-Lozano, M. A. Koopmans, F. Sullivan, P. F. Protze, J. Krause, G. Verhage, M. Li, K. W. Liu, F. Smit, A. B. Sci Adv Research Articles Synaptic transmission is the predominant form of communication in the brain. It requires functionally specialized molecular machineries constituted by thousands of interacting synaptic proteins. Here, we made use of recent advances in cross-linking mass spectrometry (XL-MS) in combination with biochemical and computational approaches to reveal the architecture and assembly of synaptic protein complexes from mouse brain hippocampus and cerebellum. We obtained 11,999 unique lysine-lysine cross-links, comprising connections within and between 2362 proteins. This extensive collection was the basis to identify novel protein partners, to model protein conformational dynamics, and to delineate within and between protein interactions of main synaptic constituents, such as Camk2, the AMPA-type glutamate receptor, and associated proteins. Using XL-MS, we generated a protein interaction resource that we made easily accessible via a web-based platform (http://xlink.cncr.nl) to provide new entries into exploration of all protein interactions identified. American Association for the Advancement of Science 2020-02-19 /pmc/articles/PMC7030922/ /pubmed/32128395 http://dx.doi.org/10.1126/sciadv.aax5783 Text en Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution License 4.0 (CC BY). http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Gonzalez-Lozano, M. A. Koopmans, F. Sullivan, P. F. Protze, J. Krause, G. Verhage, M. Li, K. W. Liu, F. Smit, A. B. Stitching the synapse: Cross-linking mass spectrometry into resolving synaptic protein interactions |
title | Stitching the synapse: Cross-linking mass spectrometry into resolving synaptic protein interactions |
title_full | Stitching the synapse: Cross-linking mass spectrometry into resolving synaptic protein interactions |
title_fullStr | Stitching the synapse: Cross-linking mass spectrometry into resolving synaptic protein interactions |
title_full_unstemmed | Stitching the synapse: Cross-linking mass spectrometry into resolving synaptic protein interactions |
title_short | Stitching the synapse: Cross-linking mass spectrometry into resolving synaptic protein interactions |
title_sort | stitching the synapse: cross-linking mass spectrometry into resolving synaptic protein interactions |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7030922/ https://www.ncbi.nlm.nih.gov/pubmed/32128395 http://dx.doi.org/10.1126/sciadv.aax5783 |
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