-
Je něco špatně v tomto záznamu ?
On multivalent receptor activity of GM1 in cholesterol containing membranes
R. Šachl, M. Amaro, G. Aydogan, A. Koukalová, II. Mikhalyov, IA. Boldyrev, J. Humpolíčková, M. Hof,
Jazyk angličtina Země Nizozemsko
Typ dokumentu časopisecké články, práce podpořená grantem
- MeSH
- buněčná membrána metabolismus MeSH
- cholesterol MeSH
- difuze MeSH
- G(M1) gangliosid chemie metabolismus MeSH
- hydraziny metabolismus MeSH
- ligandy MeSH
- metoda Monte Carlo MeSH
- ovce MeSH
- počítačová simulace MeSH
- receptory buněčného povrchu metabolismus MeSH
- rezonanční přenos fluorescenční energie MeSH
- shluková analýza MeSH
- titrace MeSH
- zvířata MeSH
- Check Tag
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
Gangliosides located at the outer leaflet of plasma membrane are molecules that either participate in recognizing of exogenous ligand molecules or exhibit their own receptor activity, which are both essential phenomena for cell communication and signaling as well as for virus and toxin entry. Regulatory mechanisms of lipid-mediated recognition are primarily subjected to the physical status of the membrane in close vicinity of the receptor. Concerning the multivalent receptor activity of the ganglioside GM1, several regulatory strategies dealing with GM1 clustering and cholesterol involvement have been proposed. So far however, merely the isolated issues were addressed and no interplay between them investigated. In this work, several advanced fluorescence techniques such as Z-scan fluorescence correlation spectroscopy, Förster resonance energy transfer combined with Monte Carlo simulations, and a newly developed fluorescence antibunching assay were employed to give a more complex portrait of clustering and cholesterol involvement in multivalent ligand recognition of GM1. Our results indicate that membrane properties have an impact on a fraction of GM1 molecules that is not available for the ligand binding. While at low GM1 densities (~1 %) it is the cholesterol that turns GM1 headgroups invisible, at higher GM1 level (~4 %) it is purely the local density of GM1 molecules that inhibits the recognition. At medium GM1 content, cooperation of the two phenomena occurs. This article is part of a Special Issue entitled: Nanoscale membrane organisation and signalling.
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc15031918
- 003
- CZ-PrNML
- 005
- 20170124161411.0
- 007
- ta
- 008
- 151005s2015 ne f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1016/j.bbamcr.2014.07.016 $2 doi
- 035 __
- $a (PubMed)25101973
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a ne
- 100 1_
- $a Šachl, Radek $u Department of Biophysical Chemistry, J. Heyrovsky Institute of Physical Chemistry of the Academy of Sciences of the Czech Republic, Dolejškova 2155/3, Prague 8, Cz-182 23, Czech Republic. Electronic address: radek.sachl@jh-inst.cas.cz. $7 xx0210158
- 245 10
- $a On multivalent receptor activity of GM1 in cholesterol containing membranes / $c R. Šachl, M. Amaro, G. Aydogan, A. Koukalová, II. Mikhalyov, IA. Boldyrev, J. Humpolíčková, M. Hof,
- 520 9_
- $a Gangliosides located at the outer leaflet of plasma membrane are molecules that either participate in recognizing of exogenous ligand molecules or exhibit their own receptor activity, which are both essential phenomena for cell communication and signaling as well as for virus and toxin entry. Regulatory mechanisms of lipid-mediated recognition are primarily subjected to the physical status of the membrane in close vicinity of the receptor. Concerning the multivalent receptor activity of the ganglioside GM1, several regulatory strategies dealing with GM1 clustering and cholesterol involvement have been proposed. So far however, merely the isolated issues were addressed and no interplay between them investigated. In this work, several advanced fluorescence techniques such as Z-scan fluorescence correlation spectroscopy, Förster resonance energy transfer combined with Monte Carlo simulations, and a newly developed fluorescence antibunching assay were employed to give a more complex portrait of clustering and cholesterol involvement in multivalent ligand recognition of GM1. Our results indicate that membrane properties have an impact on a fraction of GM1 molecules that is not available for the ligand binding. While at low GM1 densities (~1 %) it is the cholesterol that turns GM1 headgroups invisible, at higher GM1 level (~4 %) it is purely the local density of GM1 molecules that inhibits the recognition. At medium GM1 content, cooperation of the two phenomena occurs. This article is part of a Special Issue entitled: Nanoscale membrane organisation and signalling.
- 650 _2
- $a zvířata $7 D000818
- 650 _2
- $a buněčná membrána $x metabolismus $7 D002462
- 650 _2
- $a cholesterol $7 D002784
- 650 _2
- $a shluková analýza $7 D016000
- 650 _2
- $a počítačová simulace $7 D003198
- 650 _2
- $a difuze $7 D004058
- 650 _2
- $a rezonanční přenos fluorescenční energie $7 D031541
- 650 _2
- $a G(M1) gangliosid $x chemie $x metabolismus $7 D005677
- 650 _2
- $a hydraziny $x metabolismus $7 D006834
- 650 _2
- $a ligandy $7 D008024
- 650 _2
- $a metoda Monte Carlo $7 D009010
- 650 _2
- $a receptory buněčného povrchu $x metabolismus $7 D011956
- 650 _2
- $a ovce $7 D012756
- 650 _2
- $a titrace $7 D017186
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Amaro, Mariana $u Department of Biophysical Chemistry, J. Heyrovsky Institute of Physical Chemistry of the Academy of Sciences of the Czech Republic, Dolejškova 2155/3, Prague 8, Cz-182 23, Czech Republic. Electronic address: mariana.amaro@jh-inst.cas.cz. $7 gn_A_00005285
- 700 1_
- $a Aydogan, Gokcan $u Department of Biophysical Chemistry, J. Heyrovsky Institute of Physical Chemistry of the Academy of Sciences of the Czech Republic, Dolejškova 2155/3, Prague 8, Cz-182 23, Czech Republic. Electronic address: gokcan.aydogan@jh-inst.cas.cz. $7 gn_A_00010568
- 700 1_
- $a Koukalová, Alena $u Department of Biophysical Chemistry, J. Heyrovsky Institute of Physical Chemistry of the Academy of Sciences of the Czech Republic, Dolejškova 2155/3, Prague 8, Cz-182 23, Czech Republic; Faculty of Science, Charles University in Prague, Albertov 6, 128 43, Prague 2, Czech Republic. Electronic address: alenakoukalova@seznam.cz.
- 700 1_
- $a Mikhalyov, Ilya I $u Shemyakin- Ovchinnikov Institute of Bioorganic Chemistry of the Russian Academy of Science, Ul. Miklukho-Maklaya, 16/10, 117997 Moscow, GSP-7, Russian Federation. Electronic address: ilya.mikhalyov@gmail.com.
- 700 1_
- $a Boldyrev, Ivan A $u Shemyakin- Ovchinnikov Institute of Bioorganic Chemistry of the Russian Academy of Science, Ul. Miklukho-Maklaya, 16/10, 117997 Moscow, GSP-7, Russian Federation. Electronic address: ivan@lipids.ibch.ru.
- 700 1_
- $a Humpolíčková, Jana $u Department of Biophysical Chemistry, J. Heyrovsky Institute of Physical Chemistry of the Academy of Sciences of the Czech Republic, Dolejškova 2155/3, Prague 8, Cz-182 23, Czech Republic. Electronic address: jana.humpolickova@jh-inst.cas.cz.
- 700 1_
- $a Hof, Martin $u Department of Biophysical Chemistry, J. Heyrovsky Institute of Physical Chemistry of the Academy of Sciences of the Czech Republic, Dolejškova 2155/3, Prague 8, Cz-182 23, Czech Republic. Electronic address: martin.hof@jh-inst.cas.cz.
- 773 0_
- $w MED00009314 $t Biochimica et biophysica acta $x 0006-3002 $g Roč. 1853, č. 4 (2015), s. 850-7
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/25101973 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20151005 $b ABA008
- 991 __
- $a 20170124161526 $b ABA008
- 999 __
- $a ok $b bmc $g 1092794 $s 915044
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2015 $b 1853 $c 4 $d 850-7 $e 20140804 $i 0006-3002 $m Biochimica et biophysica acta $n Biochim Biophys Acta $x MED00009314
- LZP __
- $a Pubmed-20151005