Measuring membrane capacitance during a depolarizing stimulus

Regulated by the combined actions of various proteins and lipids, exocytosis in neurons or neuroendocrine cells is a highly dynamic process. It involves the transition of secretory vesicles through distinct molecular states in a time scale of seconds and final rapid Ca dependent vesicle fusion in a...

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Main Authors: Chen, Peng., Gillis, Kevin., Xue, Renhao., Pui, Tze Sian.
Other Authors: School of Chemical and Biomedical Engineering
Format: Research Report
Language:English
Published: 2010
Subjects:
Online Access:http://hdl.handle.net/10356/42274
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author Chen, Peng.
Gillis, Kevin.
Xue, Renhao.
Pui, Tze Sian.
author2 School of Chemical and Biomedical Engineering
author_facet School of Chemical and Biomedical Engineering
Chen, Peng.
Gillis, Kevin.
Xue, Renhao.
Pui, Tze Sian.
author_sort Chen, Peng.
collection NTU
description Regulated by the combined actions of various proteins and lipids, exocytosis in neurons or neuroendocrine cells is a highly dynamic process. It involves the transition of secretory vesicles through distinct molecular states in a time scale of seconds and final rapid Ca dependent vesicle fusion in a time scale of milliseconds. It is critical to resolve the highly dynamic kinetic steps along the molecular cascade of exocytosis in order to pin down the specific actions of regulatory molecules and eventually decipher this complex and fundamental process.
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spelling ntu-10356/422742023-03-03T15:30:51Z Measuring membrane capacitance during a depolarizing stimulus Chen, Peng. Gillis, Kevin. Xue, Renhao. Pui, Tze Sian. School of Chemical and Biomedical Engineering DRNTU::Engineering::Chemical engineering::Biotechnology Regulated by the combined actions of various proteins and lipids, exocytosis in neurons or neuroendocrine cells is a highly dynamic process. It involves the transition of secretory vesicles through distinct molecular states in a time scale of seconds and final rapid Ca dependent vesicle fusion in a time scale of milliseconds. It is critical to resolve the highly dynamic kinetic steps along the molecular cascade of exocytosis in order to pin down the specific actions of regulatory molecules and eventually decipher this complex and fundamental process. RG 41/05 2010-10-12T07:21:23Z 2010-10-12T07:21:23Z 2008 2008 Research Report http://hdl.handle.net/10356/42274 en 41 p. application/pdf
spellingShingle DRNTU::Engineering::Chemical engineering::Biotechnology
Chen, Peng.
Gillis, Kevin.
Xue, Renhao.
Pui, Tze Sian.
Measuring membrane capacitance during a depolarizing stimulus
title Measuring membrane capacitance during a depolarizing stimulus
title_full Measuring membrane capacitance during a depolarizing stimulus
title_fullStr Measuring membrane capacitance during a depolarizing stimulus
title_full_unstemmed Measuring membrane capacitance during a depolarizing stimulus
title_short Measuring membrane capacitance during a depolarizing stimulus
title_sort measuring membrane capacitance during a depolarizing stimulus
topic DRNTU::Engineering::Chemical engineering::Biotechnology
url http://hdl.handle.net/10356/42274
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