2011
DOI: 10.1016/j.ab.2011.05.044
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Isolation of detergent-resistant membranes from plant photosynthetic and non-photosynthetic tissues

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Cited by 27 publications
(19 citation statements)
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“…Borner et al [4] and Mongrand et al [31] first quantified lipid class and fatty acid composition using DRM as microdomain-enriched fractions. In the same way, the DRM lipid compositions of maize embryos and bean leaves have been characterized [6,7]. Furt et al [12] reported that phosphatidylinositol-4,5-bisphosphate forms a cluster-like structure that is not influenced by sterol depletion, and that phosphoinositide metabolism-related enzyme activities in DRMs are higher than in the PM.…”
Section: Introductionmentioning
confidence: 99%
“…Borner et al [4] and Mongrand et al [31] first quantified lipid class and fatty acid composition using DRM as microdomain-enriched fractions. In the same way, the DRM lipid compositions of maize embryos and bean leaves have been characterized [6,7]. Furt et al [12] reported that phosphatidylinositol-4,5-bisphosphate forms a cluster-like structure that is not influenced by sterol depletion, and that phosphoinositide metabolism-related enzyme activities in DRMs are higher than in the PM.…”
Section: Introductionmentioning
confidence: 99%
“…With a reported size of microdomains ranging from nanoscale up to microscale (Edidin, 2001; Cacas et al, 2012), direct visualization of such domains in living cells remains challenging. Sterol-dependent protein localization was reported in various plant systems (Borner et al, 2005; Roche et al, 2008; Kierszniowska et al, 2009; Minami et al, 2009; Carmona-Salazar et al, 2011; Navarro-Lérida et al, 2012) and selected proteins with sterol-dependent membrane location were shown to exhibit a patchy organization within the plasma membrane (Bariola et al, 2004; Parton and Hancock, 2004). The biological function of these microdomains was especially linked to signaling and transport processes in several independent studies (Simons and Toomre, 2000; Borner et al, 2005; Langhorst et al, 2005; Kierszniowska et al, 2009; Staubach and Hanisch, 2011; Stuermer, 2011).…”
Section: Introductionmentioning
confidence: 99%
“…The plant plasma membrane contains at least four major sterols: stigmasterol, sitosterol, campesterol, and cholesterol. For example, sitosterol and stigmasterol represent the major sterols in Arabidopsis and rice (Cooke et al 1991(Cooke et al , 1993Arnqvist et al 2008), whereas sitosterol and campesterol are two of the major sterols present in rye and maize (Cooke et al 1991(Cooke et al , 1993Bohn et al 2001;Carmona-Salazar et al 2011) and stigmasterol and cholesterol are found at the highest levels in oat (Cooke et al 1991(Cooke et al , 1993(Cooke et al , 1994. Sterols have a stabilizing effect on the membrane structure since their small polar head (the OH in the position 3 0 ) and the planar stereochemistry of their rings fulfill the voids between the other complex lipids due to bulky polar heads and unsaturations that produce deformations of acyl chains.…”
Section: Interaction With Sterols: the Planar Solutionmentioning
confidence: 99%
“…Attached to the sphingosine there is a neutral head composed of carbohydrates or an acidic head with phosphate and carbohydrates. The diversity of these two large classes of membrane complex lipids lies in the many forms of FA, LCB, and polar heads that may assemble in multiple combinations, rendering a large amount of different molecular species (Bohn et al 2001;Chen et al 2009;Carmona-Salazar et al 2011, 2015. Sterols are also diversified, as they are mainly present as sitosterol, stigmasterol, campesterol, and cholesterol (Hartmann 2004).…”
mentioning
confidence: 99%