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Keywords: lipid raft
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Biochem J (2024) 481 (24): 1997–2015.
Published: 23 December 2024
... and cholesterol, so called lipid rafts [ 4 ], have been related to signaling pathways involved in cancer progression; they can recruit or exclude signaling proteins, including kinases and phosphatases in response to external and intracellular stimuli leading to dynamic changes in cell size and composition [ 5 , 6...
Includes: Supplementary data
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Biochem J (2011) 439 (3): 497–504.
Published: 13 October 2011
...Sai P. Ramnarayanan; Pamela L. Tuma Our recent studies have been aimed at understanding the mechanisms regulating apical protein sorting in polarized epithelial cells. In particular, we have been investigating how lipid rafts serve to sort apical proteins in the biosynthetic pathway. The recent...
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Biochem J (2011) 437 (3): 483–491.
Published: 13 July 2011
...Peter Meszaros; Karin Klappe; Ina Hummel; Dick Hoekstra; Jan Willem Kok MRP1 (multidrug-resistance-related protein 1)/ABCC1 (ATP-binding cassette transporter C1) has been localized in cholesterol-enriched lipid rafts, which suggests a role for these lipid rafts and/or cholesterol in MRP1 function...
Includes: Supplementary data
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Biochem J (2010) 432 (2): 283–294.
Published: 12 November 2010
... the possibility of bi-directional cell–cell Notch signalling. In the present study we have unequivocally identified the sheddase responsible for shedding Jagged1 as ADAM17, the activity of which has previously been shown to be localized within specialized microdomains of the cell membrane known as ‘lipid rafts...
Includes: Supplementary data
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Biochem J (2010) 430 (3): e7–e9.
Published: 27 August 2010
...Nicoletta Kahya Tracking fluorescent lipids in cellular membranes has been applied for decades to shed light on membrane trafficking, sorting, endocytosis and exocytosis, viral entry, and to understand the functional relevance of membrane heterogeneity, phase separation and lipid rafts. However...
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Biochem J (2010) 430 (3): 415–423.
Published: 27 August 2010
... Journal compilation © 2010 Biochemical Society 2010 confocal fluorescence microscopy fluorescent probe giant unilamellar vesicle lipid raft liquid-ordered phase partitioning The number of fluorescence probes used for imaging membrane domains is steadily increasing [ 17 – 19 ]. However...
Includes: Supplementary data
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Biochem J (2010) 427 (3): 535–540.
Published: 14 April 2010
...Andy A. Cole; Ayse Dosemeci; Thomas S. Reese Biochemical studies have suggested that certain synaptic proteins associate with lipid rafts to perform key functions within the synapse. However, variability in biochemical preparations raises questions as to which synaptic proteins actually associate...
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Biochem J (2010) 427 (1): 79–90.
Published: 15 March 2010
... and inhibition of ERK1/2 phosphorylation by PD098059 resulted in reduced IbeA+ E. coli invasion. Fourthly, IbeA+ E. coli and IbeA-coated beads induced the clustering of vimentin that was correlated with increased entry of bacteria and beads. Lastly, IbeA+ E. coli K1 invasion was inhibited by lipid-raft...
Includes: Supplementary data
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Biochem J (2010) 425 (2): 341–351.
Published: 23 December 2009
.... We show that both proteins localize prevalently on the basolateral surface of FRT cells, in both singly and doubly transfected clones. Interestingly we found that they associate with DRMs (detergent-resistant membranes) or lipid rafts, from where they can be co-immunoprecipitated in a cholesterol...
Includes: Supplementary data
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Biochem J (2009) 424 (2): 163–167.
Published: 11 November 2009
... [email protected] ). 17 8 2009 28 9 2009 7 10 2009 7 10 2009 © The Authors Journal compilation © 2009 Biochemical Society 2009 giant plasma-membrane vesicle (GPMV) lipid raft liquid ordered Several lines of evidence, including the identification [ 1...
Includes: Supplementary data
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Biochem J (2009) 424 (2): e5–e6.
Published: 11 November 2009
...David Holowka Since evidence first appeared for ‘detergent-resistant membranes’ in the early to mid-1990s, cell biologists from a wide spectrum of biological sciences have been intrigued by the functional relevance of this indication of membrane heterogeneity, commonly referred to as ‘lipid rafts...
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Biochem J (2009) 423 (3): 343–351.
Published: 12 October 2009
...Julia Kiyan; Graham Smith; Hermann Haller; Inna Dumler The cholesterol-enriched membrane microdomains lipid rafts play a key role in cell activation by recruiting and excluding specific signalling components of cell-surface receptors upon receptor engagement. Our previous studies have demonstrated...
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Biochem J (2009) 420 (1): 93–103.
Published: 28 April 2009
..., such as signal transduction, endocytosis and protein trafficking, have been attributed to plant lipid rafts and DRMs. The data available are essentially based on proteomics and more approaches need to be undertaken to elucidate the precise function of individual populations of DRMs in plants. We report here...
Includes: Supplementary data
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Biochem J (2009) 417 (2): 525–533.
Published: 23 December 2008
... raft non-ionic detergent prion protein Thy-1 Lipid rafts are postulated to be nanodomains within the cell-surface membrane, formed by local condensation of cholesterol with saturated lipids to form distinct patches of L o (liquid ordered) phase within the general fluid ‘sea’ of L d (liquid...
Includes: Supplementary data
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Biochem J (2007) 403 (2): 313–322.
Published: 26 March 2007
...: Department of Biochemistry and Molecular Biology, University of Calgary, 3330 Hospital Drive NW, Calgary, Alberta, Canada T2N 4N1. 9 11 2006 20 12 2006 5 1 2007 5 1 2007 The Biochemical Society, London 2007 cross-linking flotillin lipid raft membrane microdomain...
Includes: Supplementary data
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Biochem J (2006) 400 (3): 401–410.
Published: 28 November 2006
...Richard R. Sprenger; Ruud D. Fontijn; Jan van Marle; Hans Pannekoek; Anton J. G. Horrevoets Lipid rafts and caveolae are biochemically similar, specialized domains of the PM (plasma membrane) that cluster specific proteins. However, they are morphologically distinct, implying different, possibly...
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Biochem J (2005) 392 (1): 29–38.
Published: 08 November 2005
... propose that the polycystin multiprotein complex is embedded in a cholesterol-containing signalling microdomain specified by flotillin-2, which is distinct from classical light-buoyant-density, detergent-resistant domains. Recent investigations determined a possible association between lipid rafts...
Includes: Supplementary data
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Biochem J (2005) 391 (3): 465–472.
Published: 25 October 2005
... in the plasma membrane, alters the properties of lipid rafts and interferes with the function of a raft-associated plasma-membrane receptor. Such a mechanism may participate in the pathogenesis of NPC disease and contribute to insulin resistance in other disorders of lipid metabolism. Cells were serum-starved...
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Biochem J (2005) 389 (1): 1–11.
Published: 21 June 2005
.... Muncke, R. G. Parton and J. F. Hancock, unpublished work). The clustering of H-rasG12V and K-rasG12V is insensitive to acute cholesterol depletion, indicating that neither domain is a classical lipid raft [ 28 ]. The minimal membrane anchor of H-ras targets GFP (GFP–tH) and mRFP (mRFP–tH) to cholesterol...
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Biochem J (2005) 385 (2): 329–337.
Published: 07 January 2005
... (ICAM-1) lipid raft transmigration vascular cell adhesion molecule-1 (VCAM-1) VE-cadherin Leucocytes need to cross the endothelium in order to enter tissues during inflammatory and immune responses [ 1 , 2 ]. Leucocyte TEM (trans-endothelial migration; also known as extravasation...
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Biochem J (2004) 381 (3): 911–917.
Published: 27 July 2004
... becomes associated with detergent-resistant membranes, indicating that it binds preferentially to lipid rafts. In the present study, we have used atomic force microscopy to examine directly the association of VacA with lipid domains in supported lipid bilayers. VacA did not bind to lipid bilayers at pH...
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Biochem J (2004) 380 (1): 181–191.
Published: 15 May 2004
... and detergent solubility studies revealed Shank2E complexed with actin and co-distributed with actin in detergent-insoluble lipid rafts. These findings indicate epithelial cells express an ankyrin repeat-containing Shank2 isoform, termed Shank2E, that is poised to co-ordinate actin-dependent events...
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Biochem J (2004) 378 (2): 641–648.
Published: 01 March 2004
... to occur early in the secretory pathway and, in agreement with this proposal, GPI-PLD activity in GPI-PLD-HeLa cells was detected not only in the endoplasmic reticulum and Golgi apparatus, but also in the plasma membrane. The enzyme was also active in lipid rafts, membrane microdomains in which GPI...
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Biochem J (2004) 378 (2): 281–292.
Published: 01 March 2004
...Linda J. PIKE Lipid rafts are membrane microdomains that are enriched in cholesterol and glycosphingolipids. They have been implicated in processes as diverse as signal transduction, endocytosis and cholesterol trafficking. Recent evidence suggests that this diversity of function is accompanied...
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Biochem J (2004) 377 (3): 741–747.
Published: 01 February 2004
... should be addressed (e-mail [email protected] ). 25 2 2003 12 9 2003 21 10 2003 21 10 2003 The Biochemical Society, London ©2004 2004 caveolae cholesteryl ester intracellular signalling lipid raft scavenger receptor class B type I Src homology 3 (SH3...
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Biochem J (2003) 373 (1): 125–132.
Published: 01 July 2003
...Gert H. HANSEN; Jens PEDERSEN; Lise-Lotte NIELS-CHRISTIANSEN; Lissi IMMERDAL; E. Michael DANIELSEN The brush border of small intestinal enterocytes is highly enriched in cholesterol- and glycosphingolipid-containing membrane microdomains, commonly termed as lipidrafts’. Functionally, transcytosis...
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Biochem J (2003) 369 (2): 199–211.
Published: 15 January 2003
... part in a metabolic flux towards sphingomyelin, diacylglycerol and glycosphingolipids, which drives lipid raft formation and vesicular transport towards the plasma membrane. At the cell surface, receptor clustering in lipid rafts and the formation of endosomes can be facilitated by transient ceramide...