Quantitative measurement of transmitters in individual vesicles in the cytoplasm of single cells with nanotip electrodes.

The quantification of vesicular transmitter content is important for studying the mechanisms of neurotransmission and malfunction in disease, and yet it is incredibly difficult to measure the tiny amounts of neurotransmitters in the attoliter volume of a single vesicle, especially in the cell environment. We introduce a novel method, intracellular vesicle electrochemical cytometry. A nanotip conical carbon-fiber microelectrode was used to electrochemically measure the total content of electroactive neurotransmitters in individual nanoscale vesicles in single PC12 cells as these vesicles lysed on the electrode inside the living cell. The results demonstrate that only a fraction of the quantal neurotransmitter content is released during exocytosis. These data support the intriguing hypothesis that the vesicle does not open all the way during the normal exocytosis process, thus resulting in incomplete expulsion of the vesicular contents.

[1]  R. Tsien,et al.  Influence of Synaptic Vesicle Position on Release Probability and Exocytotic Fusion Mode , 2012, Science.

[2]  Andrew G. Ewing,et al.  Characterizing the catecholamine content of single mammalian vesicles by collision-adsorption events at an electrode. , 2015, Journal of the American Chemical Society.

[3]  Andrew G Ewing,et al.  Hybrid capillary-microfluidic device for the separation, lysis, and electrochemical detection of vesicles. , 2009, Analytical chemistry.

[4]  R. Tsien,et al.  Single synaptic vesicles fusing transiently and successively without loss of identity , 2003, Nature.

[5]  C. Amatore,et al.  Reconstruction of aperture functions during full fusion in vesicular exocytosis of neurotransmitters. , 2010, Chemphyschem : a European journal of chemical physics and physical chemistry.

[6]  Scott N. Thorgaard,et al.  Monitoring the electrophoretic migration and adsorption of single insulating nanoparticles at ultramicroelectrodes. , 2013, The journal of physical chemistry. B.

[7]  Andrew G. Ewing,et al.  Amperometric post spike feet reveal most exocytosis is via extended kiss-and-run fusion , 2012, Scientific Reports.

[8]  Ege T. Kavalali,et al.  Kinetics and regulation of fast endocytosis at hippocampal synapses , 1998, Nature.

[9]  J. A. Jankowski,et al.  Etched carbon-fiber electrodes as amperometric detectors of catecholamine secretion from isolated biological cells. , 1991, Analytical chemistry.

[10]  C. Amatore,et al.  Vesicular release of neurotransmitters: converting amperometric measurements into size, dynamics and energetics of initial fusion pores. , 2013, Faraday discussions.

[11]  David Klenerman,et al.  Electrochemical nanoprobes for single-cell analysis. , 2014, ACS nano.

[12]  A. Ewing,et al.  VMAT-Mediated Changes in Quantal Size and Vesicular Volume , 2000, The Journal of Neuroscience.

[13]  S. Lemay,et al.  Time-resolved electrochemical detection of discrete adsorption events. , 2004, Journal of the American Chemical Society.

[14]  Zhuan Zhou,et al.  Nanoelectrode for amperometric monitoring of individual vesicular exocytosis inside single synapses. , 2014, Angewandte Chemie.

[15]  Jun Wang,et al.  Individually addressable thin-film ultramicroelectrode array for spatial measurements of single vesicle release. , 2013, Analytical chemistry.

[16]  B. Kasemo,et al.  Rupture Pathway of Phosphatidylcholine Liposomes on Silicon Dioxide , 2009, International journal of molecular sciences.

[17]  Andrew G. Ewing,et al.  Characterization of submicron-sized carbon electrodes insulated with a phenol-allylphenol copolymer , 1992 .

[18]  M. Dahan,et al.  Probing cellular events, one quantum dot at a time , 2010, Nature Methods.

[19]  Charles M. Lieber,et al.  Three-Dimensional, Flexible Nanoscale Field-Effect Transistors as Localized Bioprobes , 2010, Science.

[20]  Ning Wang,et al.  Nanoneedle: a multifunctional tool for biological studies in living cells. , 2010, Nanoscale.

[21]  D. Sulzer,et al.  Dopamine neurons release transmitter via a flickering fusion pore , 2004, Nature Neuroscience.

[22]  C. Stevens,et al.  Three modes of synaptic vesicular recycling revealed by single-vesicle imaging , 2003, Nature.

[23]  R. Tsien,et al.  The Dynamic Control of Kiss-And-Run and Vesicular Reuse Probed with Single Nanoparticles , 2009, Science.

[24]  R. Compton,et al.  Investigation of single-drug-encapsulating liposomes using the nano-impact method. , 2014, Angewandte Chemie.

[25]  Andrew G Ewing,et al.  Only a Fraction of Quantal Content is Released During Exocytosis as Revealed by Electrochemical Cytometry of Secretory Vesicles. , 2010, ACS chemical neuroscience.

[26]  W. Betz,et al.  Synaptic vesicle pools , 2005, Nature Reviews Neuroscience.

[27]  R. Jahn,et al.  Molecular machines governing exocytosis of synaptic vesicles , 2012, Nature.

[28]  B. J. Venton,et al.  Flame etching enhances the sensitivity of carbon-fiber microelectrodes. , 2008, Analytical chemistry.

[29]  M. Mirkin,et al.  Steady-state limiting currents at finite conical microelectrodes. , 2002, Analytical chemistry.

[30]  A. Andrews,et al.  The real catecholamine content of secretory vesicles in the CNS revealed by electrochemical cytometry , 2013, Scientific Reports.