Home LiteratureArticle Details
PMID: 17126911 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Three fluorescent protein voltage sensors exhibit low plasma membrane expression in mammalian cells.

Journal of neuroscience methods ·Vol. 161 ·No. 1 ·2007-03-30 ·Pages 32-8

Baker BJ, Lee H, Pieribone VA, Cohen LB, Isacoff EY, Knopfel T, Kosmidis EK

Abstract

Three first-generation fluorescent protein voltage sensitive probes (FP-voltage sensors) were characterized in mammalian cells. Flare, a Kv1.4 variant of FlaSh [Siegel MS, Isacoff EY. Neuron 1997;19(October (4)):735-41], SPARC [Ataka K, Pieribone VA. Biophys J 2002;82(January (1 Pt 1)):509-16], and VSFP-1 [Sakai R, Repunte-Canonigo V, Raj CD, Knopfel T. Eur J Neurosci 2001;13(June (12)):2314-18] were expressed, imaged and voltage clamped in HEK 293 cells and in dissociated hippocampal neurons. We were unable to detect a signal in response to changes in membrane potential after averaging16 trials with any of the three constructs. Using the hydrophobic voltage sensitive dye, di8-ANEPPS, as a surface marker, confocal analyses demonstrated poor plasma membrane expression for Flare, SPARC and VSFP-1 in both HEK 293 cells and dissociated hippocampal neurons. Almost all of the expressed FP-voltage sensors reside in internal membranes in both cell types. This internal expression generates a background fluorescence that increases the noise in the optical measurement.

MeSH Terms
Animals Cell Membrane/metabolism Cells, Cultured Coculture Techniques Electric Stimulation/methods Embryo, Mammalian Fluorescent Dyes/metabolism Gene Expression/physiology Hippocampus/cytology Humans Ion Channel Gating/physiology Kv1.4 Potassium Channel/genetics Luminescent Proteins/genetics,metabolism Membrane Potentials/physiology,radiation effects Mice Mice, Transgenic Neurons/ultrastructure Patch-Clamp Techniques/methods Transfection/methods
Chemicals
Fluorescent Dyes Kv1.4 Potassium Channel Luminescent Proteins
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Baker B J
Department of Cellular and Molecular Physiology, Yale University School of Medicine, 333 Cedar St., New Haven, CT 06520, USA. Bradley.baker@yale.edu
Lee H
Pieribone V A
Cohen L B
Isacoff E Y
Knopfel T
Kosmidis E K
Article Info
Journal
Journal of neuroscience methods
Abbr.
J Neurosci Methods
ISSN
0165-0270
Published
2007-03-30
Epub
2006-00-28
Pages
32-8
Language
English
Region
Netherlands
NLM ID
7905558
Subset
IM
Grants
NIDCD NIH HHS · DC05259 · United States
NINDS NIH HHS · NS050833 · United States
NIMH NIH HHS · R21MH064214 · United States
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com