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Synapse Development

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Cover of 'Synapse Development'

Table of Contents

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    Book Overview
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    Chapter 1 A Cell Culture System to Investigate the Presynaptic Control of Subsynaptic Membrane Differentiation at the Neuromuscular Junction.
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    Chapter 2 Co-culture Synaptogenic Assay: A New Look at Fluorescence Reporters and Technological Devices.
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    Chapter 3 Synaptogenic Assays Using Neurons Cultured on Micropatterned Substrates.
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    Chapter 4 Monitoring Synapses Via Trans-Synaptic GFP Complementation.
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    Chapter 5 Generation of Spinal Motor Neurons from Human Pluripotent Stem Cells.
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    Chapter 6 Biochemical Purification of Binding Partners of Synaptic Scaffold Proteins.
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    Chapter 7 In Situ Protein Binding Assay Using Fc-Fusion Proteins.
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    Chapter 8 Reconstitution of Synaptic SNAREs into Large Liposomes with Reduced Curvature Stress.
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    Chapter 9 Isolation of Synaptosomes, Synaptic Plasma Membranes, and Synaptic Junctional Complexes.
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    Chapter 10 Purification of Synaptosome Populations Using Fluorescence-Activated Synaptosome Sorting.
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    Chapter 11 Optimized Protocol for Imaging Cleared Neural Tissues Using Light Microscopy.
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    Chapter 12 Structured Illumination Microscopy for the Investigation of Synaptic Structure and Function.
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    Chapter 13 3D d STORM Imaging of Fixed Brain Tissue.
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    Chapter 14 Synapse Development
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    Chapter 15 3D Analysis of Synaptic Ultrastructure in Organotypic Hippocampal Slice Culture by High-Pressure Freezing and Electron Tomography.
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    Chapter 16 Analyzing Endosomal Docking, Fusion, Sorting, and Budding Mechanisms in Isolated Organelles.
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    Chapter 17 Concurrent Imaging of Receptor Trafficking and Calcium Dynamics by Spinning Disk Confocal Microscopy.
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    Chapter 18 Imaging Activity-Dependent Signaling Dynamics at the Neuronal Synapse Using FRET-Based Biosensors.
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    Chapter 19 Analyzing Structural Plasticity of Dendritic Spines in Organotypic Slice Culture.
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    Chapter 20 Using Fluorescent Markers to Estimate Synaptic Connectivity In Situ.
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    Chapter 21 Dual Anterograde and Retrograde Viral Tracing of Reciprocal Connectivity.
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    Chapter 22 Mapping Synaptic Inputs of Developing Neurons Using Calcium Imaging.
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    Chapter 23 Monosynaptic Tracing in Developing Circuits Using Modified Rabies Virus.
Attention for Chapter 12: Structured Illumination Microscopy for the Investigation of Synaptic Structure and Function.
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Chapter title
Structured Illumination Microscopy for the Investigation of Synaptic Structure and Function.
Chapter number 12
Book title
Synapse Development
Published in
Methods in molecular biology, January 2017
DOI 10.1007/978-1-4939-6688-2_12
Pubmed ID
Book ISBNs
978-1-4939-6686-8, 978-1-4939-6688-2
Authors

Soyon Hong, Daniel K. Wilton, Beth Stevens, Douglas S. Richardson

Editors

Alexandros Poulopoulos

Abstract

The neuronal synapse is a primary building block of the nervous system to which alterations in structure or function can result in numerous pathologies. Studying its formation and elimination is the key to understanding how brains are wired during development, maintained throughout adulthood plasticity, and disrupted during disease. However, due to its diffraction-limited size, investigations of the synaptic junction at the structural level have primarily relied on labor-intensive electron microscopy or ultra-thin section array tomography. Recent advances in the field of super-resolution light microscopy now allow researchers to image synapses and associated molecules with high-spatial resolution, while taking advantage of the key characteristics of light microscopy, such as easy sample preparation and the ability to detect multiple targets with molecular specificity. One such super-resolution technique, Structured Illumination Microscopy (SIM), has emerged as an attractive method to examine synapse structure and function. SIM requires little change in standard light microscopy sample preparation steps, but results in a twofold improvement in both lateral and axial resolutions compared to widefield microscopy. The following protocol outlines a method for imaging synaptic structures at resolutions capable of resolving the intricacies of these neuronal connections.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 46 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 46 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 7 15%
Researcher 7 15%
Student > Bachelor 5 11%
Other 5 11%
Student > Master 5 11%
Other 7 15%
Unknown 10 22%
Readers by discipline Count As %
Neuroscience 15 33%
Agricultural and Biological Sciences 7 15%
Biochemistry, Genetics and Molecular Biology 7 15%
Chemistry 3 7%
Medicine and Dentistry 1 2%
Other 3 7%
Unknown 10 22%