001     3462
005     20200402205541.0
024 7 _ |2 pmid
|a pmid:19072315
024 7 _ |2 DOI
|a 10.1021/la803227s
024 7 _ |2 WOS
|a WOS:000262431100061
037 _ _ |a PreJuSER-3462
041 _ _ |a eng
082 _ _ |a 670
084 _ _ |2 WoS
|a Chemistry, Multidisciplinary
084 _ _ |2 WoS
|a Chemistry, Physical
084 _ _ |2 WoS
|a Materials Science, Multidisciplinary
100 1 _ |a Fenz, S.F.
|b 0
|u FZJ
|0 P:(DE-Juel1)VDB84049
245 _ _ |a Diffusion and Intermembrane Distance: Case Study of Avidin and E-Cadherin Mediated Adhesion
260 _ _ |a Washington, DC
|b ACS Publ.
|c 2009
300 _ _ |a 1074 - 1085
336 7 _ |a Journal Article
|0 PUB:(DE-HGF)16
|2 PUB:(DE-HGF)
336 7 _ |a Output Types/Journal article
|2 DataCite
336 7 _ |a Journal Article
|0 0
|2 EndNote
336 7 _ |a ARTICLE
|2 BibTeX
336 7 _ |a JOURNAL_ARTICLE
|2 ORCID
336 7 _ |a article
|2 DRIVER
440 _ 0 |a Langmuir
|x 0743-7463
|0 4081
|y 2
|v 25
500 _ _ |a Record converted from VDB: 12.11.2012
520 _ _ |a We present a biomimetic model system for cell-cell adhesion consisting of a giant unilamellar vesicle (GUV) adhering via specific ligand-receptor interactions to a supported lipid bilayer (SLB). The modification of in-plane diffusion of tracer lipids and receptors in the SLB membrane due to adhesion to the GUV is reported. Adhesion was mediated by either biotin-neutravidin (an avidin analogue) or the extracellular domains of the cell adhesion molecule E-cadherin (Ecad). In the strong interaction (biotin-avidin) case, binding of soluble receptors to the SLB alone led to reduced diffusion of tracer lipids. From theoretical considerations, this could be attributed partially to introduction of obstacles and partially to viscous effects. Further specific binding of a GUV membrane caused additional slowing down of tracers (up to 15%) and immobilization of receptors, and led to accumulation of receptors in the adhesion zone until full coverage was achieved. The intermembrane distance was measured to be 7 nm from microinterferometry (RICM). We show that a crowding effect due to the accumulated receptors alone is not sufficient to account for the slowing downan additional friction from the membrane also plays a role. In the weak binding case (Ecad), the intermembrane distance was about 50 nm, corresponding to partial overlap of the Ecad domains. No significant change in diffusion of tracer lipids was observed upon either protein binding or subsequent vesicle binding. The former was probably due to very small effective size of the obstacles introduced into the bilayer by Ecad binding, whereas the latter was due to the fact that, with such high intermembrane distance, the resulting friction is negligible. We conclude that the effect of intermembrane adhesion on diffusion depends strongly on the choice of the receptors.
536 _ _ |a Kondensierte Materie
|c P54
|2 G:(DE-HGF)
|0 G:(DE-Juel1)FUEK414
|x 0
588 _ _ |a Dataset connected to Web of Science, Pubmed
650 _ 2 |2 MeSH
|a Avidin: chemistry
650 _ 2 |2 MeSH
|a Binding Sites
650 _ 2 |2 MeSH
|a Biomimetic Materials: chemistry
650 _ 2 |2 MeSH
|a Cadherins: chemistry
650 _ 2 |2 MeSH
|a Diffusion
650 _ 2 |2 MeSH
|a Lipid Bilayers: chemistry
650 _ 2 |2 MeSH
|a Surface Properties
650 _ 7 |0 0
|2 NLM Chemicals
|a Cadherins
650 _ 7 |0 0
|2 NLM Chemicals
|a Lipid Bilayers
650 _ 7 |0 0
|2 NLM Chemicals
|a neutravidin
650 _ 7 |0 1405-69-2
|2 NLM Chemicals
|a Avidin
650 _ 7 |a J
|2 WoSType
700 1 _ |a Merkel, R.
|b 1
|u FZJ
|0 P:(DE-Juel1)128833
700 1 _ |a Sengupta, K.
|b 2
|u FZJ
|0 P:(DE-Juel1)VDB57655
773 _ _ |a 10.1021/la803227s
|g Vol. 25, p. 1074 - 1085
|p 1074 - 1085
|q 25<1074 - 1085
|0 PERI:(DE-600)2005937-1
|t Langmuir
|v 25
|y 2009
|x 0743-7463
856 7 _ |u http://dx.doi.org/10.1021/la803227s
909 C O |o oai:juser.fz-juelich.de:3462
|p VDB
913 1 _ |k P54
|v Kondensierte Materie
|l Kondensierte Materie
|b Materie
|z entfällt bis 2009
|0 G:(DE-Juel1)FUEK414
|x 0
914 1 _ |y 2009
915 _ _ |0 StatID:(DE-HGF)0010
|a JCR/ISI refereed
920 1 _ |k IBN-4
|l Biomechanik
|d 31.12.2010
|g IBN
|0 I:(DE-Juel1)VDB802
|x 0
970 _ _ |a VDB:(DE-Juel1)109501
980 _ _ |a VDB
980 _ _ |a ConvertedRecord
980 _ _ |a journal
980 _ _ |a I:(DE-Juel1)ICS-7-20110106
980 _ _ |a UNRESTRICTED
981 _ _ |a I:(DE-Juel1)IBI-2-20200312
981 _ _ |a I:(DE-Juel1)ICS-7-20110106


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