Open Access
Fluorescent probes for detecting cholesterol-rich ordered membrane microdomains: entangled relationships between structural analogies in the membrane and functional homologies in the cell
Gérald Gaibelet
1
,
François Tercé
2
,
Sophie Allart
3
,
Chantal Lebrun
4
,
Xavier Collet
2
,
Nadège Jamin
5, 6, 7
,
Stéphane Orlowski
5, 6, 7
1
1 Theranyx SA, Marseille, France
|
2
Institut des Maladies Métaboliques et Cardiovasculaires
3
U1043 Plateau Technique d’Imagerie Cellulaire
4
Toxalim
5
Centre National de La Recherche Scientifique
6
Institut de Biologie et de Technologies de Saclay
|
Publication type: Journal Article
Publication date: 2017-02-23
scimago Q4
wos Q4
SJR: 0.165
CiteScore: 2.2
Impact factor: 1.0
ISSN: 23779098
Biochemistry
Molecular Biology
Structural Biology
Biophysics
Abstract
This review addresses the question of fluorescent detection of ordered membrane (micro) domains in living (cultured) cells, with a “practical” point of view since the situation is much more complicated than for studying model membranes. We first briefly recall the bases of model membrane structural organization involving liquid-ordered and -disordered phases, and the main features of their counterparts in cell membranes that are the various microdomains. We then emphasize the utility of the fluorescent probes derived from cholesterol, and delineate the respective advantages, limitations and drawbacks of the existing ones. In particular, besides their intra-membrane behavior, their relevant characteristics should integrate their different cellular fates for membrane turn-over, trafficking and metabolism, in order to evaluate and improve their efficiency for in-situ probing membrane microdomains in the cell physiology context. Finally, at the present stage, it appears that Bdp-Chol and Pyr-met-Chol display well complementary properties, allowing to use them in combination to improve the reliability of the current experimental approaches. But the field is still open, and there remains much work to perform in this research area.
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Total citations:
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Citations from 2024:
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(14.29%)
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GOST
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Gaibelet G. et al. Fluorescent probes for detecting cholesterol-rich ordered membrane microdomains: entangled relationships between structural analogies in the membrane and functional homologies in the cell // AIMS Biophysics. 2017. Vol. 4. No. 1. pp. 121-151.
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Gaibelet G., Tercé F., Allart S., Lebrun C., Collet X., Jamin N., Orlowski S. Fluorescent probes for detecting cholesterol-rich ordered membrane microdomains: entangled relationships between structural analogies in the membrane and functional homologies in the cell // AIMS Biophysics. 2017. Vol. 4. No. 1. pp. 121-151.
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RIS
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TY - JOUR
DO - 10.3934/biophy.2017.1.121
UR - http://www.aimspress.com/article/10.3934/biophy.2017.1.121
TI - Fluorescent probes for detecting cholesterol-rich ordered membrane microdomains: entangled relationships between structural analogies in the membrane and functional homologies in the cell
T2 - AIMS Biophysics
AU - Gaibelet, Gérald
AU - Tercé, François
AU - Allart, Sophie
AU - Lebrun, Chantal
AU - Collet, Xavier
AU - Jamin, Nadège
AU - Orlowski, Stéphane
PY - 2017
DA - 2017/02/23
PB - American Institute of Mathematical Sciences (AIMS)
SP - 121-151
IS - 1
VL - 4
SN - 2377-9098
ER -
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BibTex (up to 50 authors)
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@article{2017_Gaibelet,
author = {Gérald Gaibelet and François Tercé and Sophie Allart and Chantal Lebrun and Xavier Collet and Nadège Jamin and Stéphane Orlowski},
title = {Fluorescent probes for detecting cholesterol-rich ordered membrane microdomains: entangled relationships between structural analogies in the membrane and functional homologies in the cell},
journal = {AIMS Biophysics},
year = {2017},
volume = {4},
publisher = {American Institute of Mathematical Sciences (AIMS)},
month = {feb},
url = {http://www.aimspress.com/article/10.3934/biophy.2017.1.121},
number = {1},
pages = {121--151},
doi = {10.3934/biophy.2017.1.121}
}
Cite this
MLA
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Gaibelet, Gérald, et al. “Fluorescent probes for detecting cholesterol-rich ordered membrane microdomains: entangled relationships between structural analogies in the membrane and functional homologies in the cell.” AIMS Biophysics, vol. 4, no. 1, Feb. 2017, pp. 121-151. http://www.aimspress.com/article/10.3934/biophy.2017.1.121.