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  • Video-rate far-field optical nanoscopy dissects synaptic vesicle movement.

Video-rate far-field optical nanoscopy dissects synaptic vesicle movement.

Science (New York, N.Y.) (2008-02-23)
Volker Westphal, Silvio O Rizzoli, Marcel A Lauterbach, Dirk Kamin, Reinhard Jahn, Stefan W Hell
ABSTRACT

We present video-rate (28 frames per second) far-field optical imaging with a focal spot size of 62 nanometers in living cells. Fluorescently labeled synaptic vesicles inside the axons of cultured neurons were recorded with stimulated emission depletion (STED) microscopy in a 2.5-micrometer by 1.8-micrometer field of view. By reducing the cross-sectional area of the focal spot by about a factor of 18 below the diffraction limit (260 nanometers), STED allowed us to map and describe the vesicle mobility within the highly confined space of synaptic boutons. Although restricted within boutons, the vesicle movement was substantially faster in nonbouton areas, consistent with the observation that a sizable vesicle pool continuously transits through the axons. Our study demonstrates the emerging ability of optical microscopy to investigate intracellular physiological processes on the nanoscale in real time.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Atto 647N azide, BioReagent, suitable for fluorescence
Sigma-Aldrich
Atto 647N amine, BioReagent, suitable for fluorescence
Supelco
Atto 647N maleimide, BioReagent, suitable for fluorescence, ≥90% (HPLC)
Sigma-Aldrich
Atto 647N-Biotin, BioReagent, suitable for fluorescence, ≥90.0% (HPLC)
Sigma-Aldrich
Atto 647N NHS ester, BioReagent, suitable for fluorescence, ≥90% (HPLC)
Supelco
Atto 647N, BioReagent, suitable for fluorescence, ≥90.0% (HPLC)