Vesicular neurotransmitters exocytosis monitored by amperometry: theoretical quantitative links between experimental current spikes shapes and intravesicular structures-Reference-Cited by-同舟云学术

Vesicular neurotransmitters exocytosis monitored by amperometry: theoretical quantitative links between experimental current spikes shapes and intravesicular structures

Published:2024 Issue:34 Volume:15 Page:13909-13922
ISSN:2041-6520
Container-title:Chemical Science
language:en
Short-container-title:Chem. Sci.

Author:

Dannaoui Reina¹,Hu Ren²^ORCID,Hu Lihui¹,Tian Zhong-Qun²^ORCID,Svir Irina¹^ORCID,Huang Wei-Hua³^ORCID,Amatore Christian¹²^ORCID,Oleinick Alexander¹^ORCID

Affiliation:

1. Département de Chimie, PASTEUR, Ecole Normale Supérieure, PSL Université, Sorbonne Université, CNRS, 24 rue Lhomond, Paris 75005, France

2. State Key Laboratory of Physical Chemistry of Solid Surfaces, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, P.R. China

3. College of Chemistry and Molecular Sciences, Wuhan University, Wuhan 430072, P.R. China

Abstract

Single-cell amperometry: theoretical analysis of individual exocytotic spikes with two-exponential decay tails provides insights into intravesicular structure.

Funder

École Normale Supérieure

Sorbonne Université

National Natural Science Foundation of China

Centre National de la Recherche Scientifique

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/SC/D4SC04003A

Reference62 articles.

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2. Analysis of diffusional broadening of vesicular packets of catecholamines released from biological cells during exocytosis

3. Temporally resolved, independent stages of individual exocytotic secretion events

4. Temporally resolved catecholamine spikes correspond to single vesicle release from individual chromaffin cells.

5. Real-time Monitoring of Discrete Synaptic Release Events and Excitatory Potentials within Self-reconstructed Neuromuscular Junctions