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Quantifying molecular aggregation by super resolution microscopy within an excitatory synapse from mouse hippocampal neurons

Super-resolution microscopy (SRM) has been widely adopted to probe molecular distribution at excitatory synapses. We present an SRM paradigm to evaluate the nanoscale organization heterogeneity between neuronal subcompartments. Using mouse hippocampal neurons, we describe the identification of the m...

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Detalles Bibliográficos
Autores principales: Kedia, Shekhar, Ramanan, Narendrakumar, Nair, Deepak
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8076707/
https://www.ncbi.nlm.nih.gov/pubmed/33937876
http://dx.doi.org/10.1016/j.xpro.2021.100470
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author Kedia, Shekhar
Ramanan, Narendrakumar
Nair, Deepak
author_facet Kedia, Shekhar
Ramanan, Narendrakumar
Nair, Deepak
author_sort Kedia, Shekhar
collection PubMed
description Super-resolution microscopy (SRM) has been widely adopted to probe molecular distribution at excitatory synapses. We present an SRM paradigm to evaluate the nanoscale organization heterogeneity between neuronal subcompartments. Using mouse hippocampal neurons, we describe the identification of the morphological characteristics of nanodomains within functional zones of a single excitatory synapse. This information can be used to correlate structure and function at molecular resolution in single synapses. The protocol can be applied to immunocytochemical/histochemical samples across different imaging paradigms. For complete details on the use and execution of this protocol, please refer to Kedia et al. (2021).
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spelling pubmed-80767072021-04-29 Quantifying molecular aggregation by super resolution microscopy within an excitatory synapse from mouse hippocampal neurons Kedia, Shekhar Ramanan, Narendrakumar Nair, Deepak STAR Protoc Protocol Super-resolution microscopy (SRM) has been widely adopted to probe molecular distribution at excitatory synapses. We present an SRM paradigm to evaluate the nanoscale organization heterogeneity between neuronal subcompartments. Using mouse hippocampal neurons, we describe the identification of the morphological characteristics of nanodomains within functional zones of a single excitatory synapse. This information can be used to correlate structure and function at molecular resolution in single synapses. The protocol can be applied to immunocytochemical/histochemical samples across different imaging paradigms. For complete details on the use and execution of this protocol, please refer to Kedia et al. (2021). Elsevier 2021-04-14 /pmc/articles/PMC8076707/ /pubmed/33937876 http://dx.doi.org/10.1016/j.xpro.2021.100470 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Protocol
Kedia, Shekhar
Ramanan, Narendrakumar
Nair, Deepak
Quantifying molecular aggregation by super resolution microscopy within an excitatory synapse from mouse hippocampal neurons
title Quantifying molecular aggregation by super resolution microscopy within an excitatory synapse from mouse hippocampal neurons
title_full Quantifying molecular aggregation by super resolution microscopy within an excitatory synapse from mouse hippocampal neurons
title_fullStr Quantifying molecular aggregation by super resolution microscopy within an excitatory synapse from mouse hippocampal neurons
title_full_unstemmed Quantifying molecular aggregation by super resolution microscopy within an excitatory synapse from mouse hippocampal neurons
title_short Quantifying molecular aggregation by super resolution microscopy within an excitatory synapse from mouse hippocampal neurons
title_sort quantifying molecular aggregation by super resolution microscopy within an excitatory synapse from mouse hippocampal neurons
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8076707/
https://www.ncbi.nlm.nih.gov/pubmed/33937876
http://dx.doi.org/10.1016/j.xpro.2021.100470
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