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Updated: Sep 25, 2025

Simultaneous Two-photon In Vivo Imaging of Synaptic Inputs and Postsynaptic Targets in the Mouse Retrosplenial Cortex
Published on: March 13, 2016
Multimodal imaging of synaptic vesicles with a single probe.
Seong J An1,2, Massimiliano Stagi3,4,5,6, Travis J Gould2,7
1Department of Cellular and Molecular Physiology, Yale University School of Medicine, New Haven, CT 06510, USA.
Researchers developed a versatile synaptic vesicle probe using a C2 domain. This single, modular probe allows imaging across multiple microscopy techniques, aiding the study of synaptic vesicle recycling and membrane dynamics.
Area of Science:
- Neuroscience
- Cell Biology
- Biochemistry
Background:
- Understanding synaptic-vesicle recycling is crucial for neuroscience.
- Current microscopy probes often target specific modalities, limiting comprehensive analysis.
- A need exists for versatile probes to study vesicle dynamics across different resolutions.
Purpose of the Study:
- To develop a single, modular probe for imaging synaptic vesicles using multiple microscopy techniques.
- To overcome limitations of modality-specific probes in studying vesicle recycling.
- To provide a tool for high-resolution imaging of synaptic vesicle function.
Main Methods:
- Utilized the membrane-binding C2 domain of cytosolic phospholipase A2 (cPLA2).
- Conjugated the C2 domain with various detectable tags.
- Demonstrated imaging of synaptic vesicles with the modular probe.
Main Results:
- A single, modular probe based on the cPLA2 C2 domain was successfully created.
- The probe enabled synaptic vesicle imaging across multiple spatial and temporal resolutions.
- The C2 domain functions as a general endocytic marker.
Conclusions:
- The developed cPLA2 C2 domain probe offers a versatile tool for synaptic vesicle research.
- This modular probe complements existing tools for studying vesicle recycling and membrane dynamics.
- The C2 domain's utility extends to studying membrane recycling in diverse cell types.
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