ライフサイエンスコーパス: outer leaflet

1 rge at the inner leaflet exceeds that at the outer leaflet.

2 end into the hydrocarbon chain region of the outer leaflet.

3 n the inner leaflet and a single site in the outer leaflet.

4 ing a majority of lipopolysaccharides in its outer leaflet.

5 d GM3 (monosialodihexosylganglioside) in the outer leaflet.

6 dylcholine (PC) family from the inner to the outer leaflet.

7 formation of nano-clusters of GM3 within the outer leaflet.

8 y to alter the surface electrostatics of the outer leaflet.

9 inner leaflet and sphingomyelin (SM) in the outer leaflet.

10 phipathic LPS molecules across the OM to the outer leaflet.

11 the extracted lipids were from the membrane outer leaflet.

12 r translocation of MPD from the inner to the outer leaflet.

13 nd defective redistribution of sterol to the outer leaflet.

14 LPS) comprise the hydrophobic portion of the outer leaflet.

15 he induction of inner leaflet domains by the outer leaflet.

16 ria contains lipopolysaccharide (LPS) in the outer leaflet.

17 x glycolipid lipopolysaccharide (LPS) in the outer leaflet.

18 ation of ceramide within the plasma membrane outer leaflet.

19 f diblock copolymer and an independent lipid outer leaflet.

20 ation of phospholipids from the inner to the outer leaflet.

21 ted galactosylceramide from the inner to the outer leaflet.

22 l asymmetry of 0.63 +/- 0.04 in favor of the outer leaflet.

23 the inner leaflet but not of the IMPs of the outer leaflet.

24 ts the longitudinal diffusion of IMPs of the outer leaflet.

25 inner leaflet and lipopolysaccharides in the outer leaflet.

26 a unique lipid bilayer containing LPS in its outer leaflet.

27 lipid bilayer with lipopolysaccharide in the outer leaflet.

28 the delivery of exogenous lipids to the cell outer leaflet.

29 cellular envelope and is assembled at the OM outer leaflet.

30 leaflet and lipopolysaccharides (LPS) in the outer leaflet.

31 osition mimics the mammalian plasma membrane outer leaflet.

32 between the physical states of the inner and outer leaflets.

33 ral perturbation moved through the inner and outer leaflets.

34 aflet and lipopolysaccharides comprising the outer leaflet (1-3) .

35 observe an enrichment of cholesterol in the outer leaflet and a general non-ideal lateral mixing of

36 line (POPC) as the predominant lipids in the outer leaflet and dioleoylphosphatidylcholine (DOPC), PO

37 tive pressure in the headgroup region of the outer leaflet and increasing the positive pressure throu

38 distribution with lipopolysaccharides at the outer leaflet and phospholipids (PLs) at the inner leafl

39 th lipopolysaccharides (LPS) residing in the outer leaflet and phospholipids (PLs) in the inner leafl

40 composed of lipopolysaccharide (LPS) in the outer leaflet and phospholipids in the inner leaflet.

41 ne, with lipopolysaccharide molecules in the outer leaflet and phospholipids in the inner leaflet.

42 FFA into vesicles containing both FPE in the outer leaflet and pyranine trapped in the inside aqueous

43 species including the glycolipid GM3 in the outer leaflet and the anionic lipid, phosphatidylinosito

44 n a cavity that is open to both the membrane outer leaflet and the periplasm.

45 Then the coupling between the hardened outer leaflet and the softer inner leaflet generates ben

46 Outer-leaflet and total fractions of PG were determined

47 However, LPS is found in the outer leaflet, and RcsF was thought to be tethered to th

48 DOPC (dioleoylphosphatidylcholine) in their outer leaflets, and DOPC in their inner leaflets.

49 ght to pass through hemifusion, in which the outer leaflets are fused while the inner leaflets engage

50 and thereby stress small unilamellar vesicle outer leaflets as well as the periphery of intermediate

51 ions when alphaSyn is bound to the vesicle's outer leaflet at a 200:1 L/P.

52 only the outer leaflet of the bilayer, this outer leaflet becomes more ordered, and thus more solid-

53 Owing to its outer leaflet binding, Pro12A is much more sensitive to

54 usion of TMPs and IMPs of both the inner and outer leaflets by changing the density of TMPs.

55 Surprisingly, outer leaflet components characteristically associated w

56 dynamic, large-scale uncoupling of inner and outer leaflet components of lipid rafts.

57 mbrane of gram-negative bacteria contains an outer leaflet composed of lipopolysaccharide (LPS) that

58 mentioned nonextractable cardiolipin and its outer leaflet composed of trehalose dimycolates, phospha

59 Lipopolysaccharide (LPS) is the major outer leaflet constituent of the Gram-negative outer mem

60 The outer leaflet contained a mixture of sphingomyelin (SM)

61 The second lipid arises from the outer leaflet coordinate between two E protein helices.

62 UVs, lateral diffusion in the bSM-containing outer leaflet decreased, whereas that in the DOPC-contai

63 nes, the lipid compositions of the inner and outer leaflets differ.

64 In addition, reduced outer-leaflet diffusion upon introduction of outer-leafl

65 In the outer leaflet, distinct nanodomains consisting of gangli

66 Approximately 80-100% replacement of outer leaflet DOPE and POPS was achieved.

67 For asymmetric vesicles with outer-leaflet egg SM or milk SM, a fluorescent lipid wit

68 distinct waves, presumably hemifusion of the outer leaflet followed by inner leaflet (core) fusion.

69 However, the SM-rich outer leaflet formed an ordered state, melting with a mi

70 ed residues in the vicinity of the inner and outer leaflet head-groups.

71 y flipped across the liposome bilayer to the outer leaflet in the presence of Mg(2+)-ATP, whereas no

72 The presence of phosphatidylcholine in the outer leaflet increased the cholesterol concentration re

73 At room temperature, SM exchange into the outer leaflet increased the inner leaflet lipid order, s

74 veral assays showed that the ordering of the outer leaflet induced by the presence of SM was not refl

75 osphatidylserine (PS) to the plasma membrane outer leaflet is a nearly universal marker of apoptosis

76 unique asymmetric lipid bilayer in which the outer leaflet is composed of lipopolysaccharide (LPS) an

77 The OM outer leaflet is comprised of endotoxin containing lipid

78 In contrast, the outer leaflet is enriched in phosphatidylglycerol and ca

79 Analysis of the lipid composition of the outer leaflet is important for understanding cell membra

80 ular the exclusion of phospholipids from the outer leaflet, is key to creating an almost impenetrable

81 Our approaches using inner- and outer-leaflet-labeled fluorescent vesicles and (1)H NMR

82 To model its outer leaflet, Langmuir monolayers and cushioned support

83 e outer leaflet of brain SM, which decreased outer-leaflet lateral diffusion, had little effect upon

84 Asymmetry of inner and outer leaflet lipid composition is an important characte

85 ously defined for erythrocytes, as judged by outer leaflet lipid composition; and plasma membrane out

86 fected, we found that C8-PI(3,5)P(2) blocked outer leaflet lipid mixing.

87 without a targeting ligand anisamide, in the outer leaflet lipid mixture.

88 le neutral or cationic lipid was used as the outer leaflet lipid to form an asymmetric lipid bilayer

89 on of lipid asymmetry by partial exchange of outer-leaflet lipid, 4) verification of lipid asymmetry

90 envelope protein induced mixing of membrane outer leaflet lipids but did not lead to content mixing,

91 ids from the asymmetric vesicles or only the outer leaflet lipids from the asymmetric vesicles.

92 stant rafts exhibited a balance of inner and outer leaflet lipids, whereas the Triton X-100 rafts con

93 or inclusion into rafts occurs mainly on the outer leaflet lipids.

94 ton X-100 rafts contained a preponderance of outer leaflet lipids.

95 consists of inner leaflet phospholipids and outer leaflet lipopolysaccharides (LPS).

96 /PSs/Chol also exhibit lo phases adjacent to outer leaflet lo phases.

97 re not induced to form lo phases by adjacent outer leaflet lo phases.

98 This indicates that inner- and outer-leaflet Lo domains can have significantly differen

99 Here, we characterize how outer-leaflet Lo domains induce inner-leaflet-ordered do

100 For asymmetric vesicles containing egg SM, outer-leaflet Lo domains were also depleted in a saturat

101 on-enhanced coupling resulting in inner- and outer-leaflet Lo domains with similar physical propertie

102 um, promotes the lipid exchange of the fused outer leaflets mediated by lipid diffusion.

103 t the two populations of cells have distinct outer leaflet membrane compositions with the membranes o

104 was no detectable coupling between inner and outer leaflet membrane order.

105 nes, communication between inner leaflet and outer leaflet, membrane adhesion, and raft mobility.

106 ted at the cell surface mediated hemifusion (outer leaflet merger) upon low-pH treatment, but only th

107 outer-leaflet diffusion upon introduction of outer-leaflet milk SM or a synthetic C24:0 SM, both of w

108 contrast, in asymmetric vesicles containing outer-leaflet milk SM, which has long acyl chains capabl

109 PS exposure at the outer leaflet occurs early in apoptosis, but it is also

110 the wedging of its long alpha-helix into the outer leaflet of a membrane may cause curvature and an a

111 ping and to redistribute lipids added to the outer leaflet of ATG9 vesicles, thereby enabling growth

112 sequesters cell wall precursors found in the outer leaflet of bacterial plasma membranes, Lipid II an

113 The presence in the outer leaflet of brain SM, which decreased outer-leaflet

114 aberrant lipid composition presented on the outer leaflet of cancer cell membranes, which makes the

115 bined enrichment of both these lipids in the outer leaflet of cancer cells is highly significant for

116 cess serine (phosphatidylserine (PS)) on the outer leaflet of cancer cells.

117 1% of the human proteome is anchored to the outer leaflet of cell membranes via a class of glycolipi

118 amine, two aminophospholipids exposed on the outer leaflet of dead and activated cells, has shed new

119 hosphatidylcholine, which is enriched in the outer leaflet of eukaryotic cells, are not well understo

120 th lipopolysaccharide (LPS) constituting the outer leaflet of Gram-negative bacteria.

121 n planar bilayer patches originated from the outer leaflet of GUVs.

122 placement of lipopolysaccharide (LPS) in the outer leaflet of its outer membrane.

123 The OM comprises an outer leaflet of lipid A, the bioactive component of lip

124 ment of drug substrate from inner leaflet to outer leaflet of lipid bilayer.

125 tained probe, Pro12A, stains exclusively the outer leaflet of lipid bilayers of liposomes, as evidenc

126 phiphile that spontaneously inserts into the outer leaflet of lipid bilayers to bury its hydrophobic

127 atidylethanolamine (FPE) introduced into the outer leaflet of lipid vesicles was used to monitor FFA

128 ith an inner leaflet of phospholipids and an outer leaflet of lipopolysaccharide.

129 The OM is asymmetric and contains an outer leaflet of lipopolysaccharides (LPS) or lipooligos

130 A(2) rapidly hydrolyzed phospholipids in the outer leaflet of liposomes and proteoliposomes with a ha

131 ids are cell-type-specific components of the outer leaflet of mammalian plasma membranes.

132 n, glucose 6-phosphate releases HKI from the outer leaflet of mitochondria; however, the site of gluc

133 The outer leaflet of neuronal membranes is highly enriched i

134 eaflet showed that PS already existed in the outer leaflet of null spermatozoa before sperm capacitat

135 GIPC) sphingolipids that are abundant in the outer leaflet of plant plasma membranes.

136 nction in preventing appearance of PS in the outer leaflet of plasma membrane, and ectopic exposure o

137 th lipid compositions typically found in the outer leaflet of plasma membranes induce liquid-ordered

138 containing glycosphingolipids present in the outer leaflet of plasma membranes, are produced at high

139 cyanine lipid analogs in the plasma membrane outer leaflet of RBL mast cells was used to investigate

140 nge to characterize the phospholipids in the outer leaflet of red blood cells (RBCs) is reported.

141 ne, a phagocyte recognition marker, from the outer leaflet of senescent RBCs.

142 l (DOPC/DPPC/Chol), which is a model for the outer leaflet of the animal cell plasma membrane.

143 This glycolipid is found exclusively in the outer leaflet of the asymmetric outer membrane (OM), whe

144 Two residues located in the outer leaflet of the bilayer are critical for fusion.

145 rcellular spaces and that lens lipids in the outer leaflet of the bilayer bind to that calcium.

146 g of wt20, which is known to affect only the outer leaflet of the bilayer, this outer leaflet becomes

147 ile daunorubicin is stably inserted into the outer leaflet of the bilayer, verapamil dynamically flip

148 syn penetrates approximately 9-14 A into the outer leaflet of the bilayer, with a substantial portion

149 4 charges with membrane phospholipids in the outer leaflet of the bilayer.

150 arrow region of 10-15 A corresponding to the outer leaflet of the bilayer.

151 nzyme from intracellular compartments to the outer leaflet of the cell membrane, where hydrolysis of

152 osphocholine and DiI have been imaged on the outer leaflet of the cell membrane, while phosphocholine

153 A is a 30-kDa protein, lipid anchored to the outer leaflet of the cell membrane.

154 ion that anchors the modified protein in the outer leaflet of the cell membrane.

155 many eukaryotic proteins that reside in the outer leaflet of the cell membrane.

156 d DiI, a fluorescent dye that remains in the outer leaflet of the cell membrane.

157 ught to power the extraction of LPS from the outer leaflet of the cytoplasmic membrane and its transp

158 d within a coiled-coil domain of Rz near the outer leaflet of the cytoplasmic membrane and were not a

159 Abundant lipoproteins cover the outer leaflet of the cytoplasmic membrane, in contrast t

160 al and the lipid attaches the protein to the outer leaflet of the cytoplasmic membrane.

161 l wall dd-carboxypeptidase, localized in the outer leaflet of the cytosolic membrane of this Gram-neg

162 ermore, phospholipid synthesis "refills" the outer leaflet of the endoplasmic reticulum (ER) membrane

163 ell-derived exosomes and is localized on the outer leaflet of the exosomal membrane.

164 Kdo) is an essential component of LPS in the outer leaflet of the Gram-negative bacterial outer membr

165 hey fail to make productive contact with the outer leaflet of the host target membrane.

166 huttling hopanoid virulence factors from the outer leaflet of the inner membrane to the periplasm.

167 e faces, RS is associated primarily with the outer leaflet of the inner segment plasma membrane throu

168 ng conformation with two portals open to the outer leaflet of the membrane and a unique topology of t

169 In ECVs, the outer leaflet of the membrane bilayer contains aminophos

170 of phosphatidylserine from the inner to the outer leaflet of the membrane bilayer during platelet ac

171 PS) externalization has been observed on the outer leaflet of the membrane shortly after nsPEF exposu

172 bstrates, phosphatidylserine exposure on the outer leaflet of the membrane, and loss of viability.

173 lipooligosaccharide (LOS) exclusively in the outer leaflet of the membrane, establishes an impermeabl

174 appearance of phosphatidylserine (PS) in the outer leaflet of the membrane.

175 hat PIP2 lipids were being desorbed from the outer leaflet of the membrane.

176 lipid droplets are thought to form from the outer leaflet of the microsomal membrane, the reduction

177 membrane protein that is associated with the outer leaflet of the mitochondrial outer membrane.

178 t mislocalized glycerophospholipids from the outer leaflet of the OM and return them to the inner mem

179 sh chemical treatments accumulate PLs in the outer leaflet of the OM and this disrupts lipopolysaccha

180 oprotein that removes phospholipids from the outer leaflet of the OM of Escherichia coli, increases O

181 ert LPS from the periplasm directly into the outer leaflet of the OM to establish the asymmetry of th

182 assembled with divalent metal cations in the outer leaflet of the OM to form an impervious layer that

183 ransport of misplaced phospholipids from the outer leaflet of the OM to the cytoplasmic membrane (4)

184 D form a complex that assembles LPS into the outer leaflet of the OM.

185 across the periplasm, and insertion into the outer leaflet of the OM.

186 hat serves to prevent PL accumulation in the outer leaflet of the OM.

187 As a result of DAGK presence in the outer leaflet of the outer envelope membrane, phosphatid

188 S), a glucosamine-based phospholipid, in the outer leaflet of the outer membrane (OM).

189 Lipid A species comprise the bulk of the outer leaflet of the outer membrane and are produced thr

190 We found that the outer leaflet of the outer membrane contains a similar n

191 s of lipopolysaccharides that constitute the outer leaflet of the outer membrane in Gram-negative bac

192 e (LPS), a glycolipid that forms most of the outer leaflet of the outer membrane in Gram-negative bac

193 highly acylated saccharolipid located on the outer leaflet of the outer membrane of Gram-negative bac

194 endotoxin) is an essential component of the outer leaflet of the outer membrane of gram-negative bac

195 The negative surface charge of the outer leaflet of the outer membrane of Gram-negative bac

196 lipid anchor of a lipopolysaccharide in the outer leaflet of the outer membrane of Gram-negative bac

197 The outer leaflet of the outer membrane of the Gram-negative

198 Similar to most Gram-negative bacteria, the outer leaflet of the outer membrane of Vibrio cholerae i

199 lipid A of the LPS may be inserted into the outer leaflet of the outer membrane through a lateral op

200 ase subunits reveals that they reside on the outer leaflet of the outer membrane under anaerobic cond

201 slocated lipoprotein that is anchored in the outer leaflet of the outer membrane, with its C-terminal

202 to terminal reductase enzymes located on the outer leaflet of the outer membrane.

203 The outer leaflet of the outer membranes of Gram-negative ba

204 lucosamine-based phospholipids that form the outer leaflet of the outer membranes of Gram-negative ba

205 choring of these surface lipoproteins in the outer leaflet of the outer spirochetal membrane.

206 t LPS induced translocation of ASMase to the outer leaflet of the plasma membrane and reduced SM leve

207 lasma membrane induced exposure of PS on the outer leaflet of the plasma membrane at sites of egress,

208 X2 or tNOX), associated exclusively with the outer leaflet of the plasma membrane at the surface of c

209 ect traversing of CPPs through the uncharged outer leaflet of the plasma membrane bilayer is unlikely

210 ion, we show that coupling may extend to the outer leaflet of the plasma membrane by examining the fl

211 ion with the GM1 ganglioside receptor in the outer leaflet of the plasma membrane in intestinal (HT-2

212 quid disorder heterogeneity of lipids in the outer leaflet of the plasma membrane in live cells.

213 imited exposure of aminophospholipids on the outer leaflet of the plasma membrane is a fundamental fe

214 ystems showed that sphingomyelin (SM) in the outer leaflet of the plasma membrane is responsible for

215 monstrated that the lipid composition of the outer leaflet of the plasma membrane is sufficient for t

216 hatidylethanolamine, that are exposed on the outer leaflet of the plasma membrane of dead and activat

217 PS), 2 phospholipids that translocate to the outer leaflet of the plasma membrane of dead cells, as t

218 agged annexin V to phosphatidylserine in the outer leaflet of the plasma membrane of degranulated mas

219 e the sphingolipids and phospholipids in the outer leaflet of the plasma membrane of living mammalian

220 It was found to cluster on the outer leaflet of the plasma membrane of the photorecepto

221 d signaling molecules typically float in the outer leaflet of the plasma membrane or freely diffuse a

222 Lipids enriched in the outer leaflet of the plasma membrane oscillated in a hig

223 and phosphatidylserine (PS) exposure on the outer leaflet of the plasma membrane preceded loss of PM

224 of unknown function that is retained on the outer leaflet of the plasma membrane when MCs are activa

225 by this flippase causing PS exposure on the outer leaflet of the plasma membrane without disrupting

226 livery of acid sphingomyelinase (ASM) to the outer leaflet of the plasma membrane, and a rapid form o

227 which is a glycosphingolipid residing on the outer leaflet of the plasma membrane, and acetylcholine

228 id not interact with liposomes mimicking the outer leaflet of the plasma membrane, but it did induce

229 from the inner (cytoplasmic) leaflet to the outer leaflet of the plasma membrane, delivering Glc2-DA

230 The enzyme, peculiarly localized on the outer leaflet of the plasma membrane, has been shown to

231 membranes and, most interestingly, with the outer leaflet of the plasma membrane, suggesting a role

232 id phosphatidylserine (PS) is exposed on the outer leaflet of the plasma membrane.

233 on that anchors the modified proteins in the outer leaflet of the plasma membrane.

234 lserine to translocate from the inner to the outer leaflet of the plasma membrane.

235 atidylserine translocation from the inner to outer leaflet of the plasma membrane.

236 rm an important class of lipids found in the outer leaflet of the plasma membrane.

237 ively charged phosphatidylserine (PS) on the outer leaflet of the plasma membrane.

238 a glycosylphosphatidylinositol anchor to the outer leaflet of the plasma membrane.

239 to PIP2 redistribution from the inner to the outer leaflet of the plasma membrane.

240 to selectively oxidize MPD molecules in the outer leaflet of the reconstituted vesicles, we demonstr

241 used to anchor a synthetic transducer in the outer leaflet of the vesicles, and when the protein was

242 had been translocated from the inner to the outer leaflet of the vesicles.

243 n of the midspan Arg (694) "snorkels" to the outer leaflet of the viral membrane, the MSD assumes a m

244 ed viruses display phosphatidylserine on the outer leaflet of their membranes, enabling TAM receptor

245 changed lipids in the aGUVs are found in the outer leaflet of these asymmetric vesicles.

246 phosphatidylserine (PtdSer) exposure on the outer leaflet of transduced cells triggers their engulfm

247 l-phosphatidylcholine was exchanged into the outer leaflet of vesicles composed of 1,2-dioleoyl-phosp

248 ich the physical properties of the inner and outer leaflets of a bilayer are coupled to one another.

249 t) and cardiolipin (present in the inner and outer leaflets of bacterial membranes).

250 and cholesterol composition in the inner and outer leaflets of biological membranes.

251 Variations between the inner and outer leaflets of cell membranes are crucial for cell fu

252 proximately 1:1 if only the PG lipids in the outer leaflets of membranes are accessible to daptomycin

253 Inner and outer leaflets of the bilayer are affected nearly equall

254 through hemifusion, a condition in which the outer leaflets of the bilayers are mixed, but the inner

255 differences in tension between the inner and outer leaflets of the membrane contribute to this proces

256 nthesizing major components of the inner and outer leaflets of the mycobacterial outer membrane.

257 species are segregated between the inner and outer leaflets of the plasma membrane by ATP-dependent l

258 the context of lipid rafts at the inner and outer leaflets of the plasma membrane, respectively, for

259 en lateral domains and between the inner and outer leaflets of the plasma membrane.

260 During membrane fusion, the outer leaflets of the two membranes merge first, whereas

261 luorescent dyes to monitor the inner and the outer leaflets of the unsupported aGUVs.

262 ried as glycoproteins and glycolipids on the outer leaflets of their plasma membranes and constitute

263 usion intermediate, a condition in which the outer leaflets of two bilayers are combined and the inne

264 ially binds to mammalian cell membranes, the outer leaflets of which are enriched in sphingomyelin, c

265 oyl-sn-glycero-3-phospho-rac-glycerol in the outer leaflet only was quantified by zeta-potential meas

266 a cholesterol analogue was localized to the outer leaflet only, the fast diffusion of cholesterol di

267 s also significantly lower than the D in the outer leaflet or in giant unilamellar vesicles and the d

268 ster, indicative of coupling between SM-rich outer-leaflet-ordered domains and inner-leaflet-ordered

269 aflet lipid composition; and plasma membrane outer leaflet phosphatidylcholine had a significantly lo

270 Furthermore, in all raft preparations, the outer leaflet phospholipid species were significantly di

271 eaflet phospholipids to the pore, but allows outer leaflet phospholipids to bind to a pronounced ridg

272 d transport protein that selectively removes outer leaflet phospholipids to help maintain the essenti

273 How outer leaflet plasma membrane components, including glyc

274 brane, but some sickle RBCs expose PS in the outer leaflet (PS+ cells).

275 oon as FPE detects adsorption of FA into the outer leaflet, pyranine detects its movement to the inne

276 red domain formation in the SM+PC-containing outer leaflet relative to ordered domain stability in ch

277 s coupled across the water layer, while the "outer" leaflets remain unaffected.

278 ol POPE:POPS inside (SMo/2:1 POPE:POPSi) the outer leaflet SM formed an ordered state with a thermal

279 In other words, ordered state formation by outer-leaflet SM in asymmetric vesicles was not destabil

280 anoparticles was held at a distance from the outer leaflet-solution interface of bilayers containing

281 tent and location of binding relative to the outer leaflet-solution interface.

282 sF/OMP complexes are required for sensing OM outer leaflet stress.

283 within the TMD region spanning the vesicle's outer leaflet strongly impairs exocytosis and decelerate

284 characteristic time of lipid mixing between outer leaflets (tau approximately equal to 24 s) was com

285 redistributes lysosomal-derived PS to the PM outer leaflet that leads to membrane expansion and the f

286 ect phospholipid packing modification in the outer leaflet, that is promoted by protonation of cardio

287 morphology and surface electrostatics of the outer leaflet, the insertion of ACs, in particular their

288 e bilayer: upon hemifusion and mixing of the outer leaflets, the DNA-lipid is free to diffuse into th

289 sphingomyelin resided in the plasma membrane outer leaflet; the asymmetry of metabolically active cel

290 ethanolamine and phosphatidylserine from the outer leaflet to the cytosolic leaflet of the plasma mem

291 luorescent PtdIns(3,4)P(2) can flip from the outer leaflet to the inner leaflet of the membrane.

292 diffusion of annular lipids in the inner and outer leaflets was observed and correlated with an asymm

293 (asymmetric) compositions in their inner and outer leaflets were deposited at surface pressures of 20

294 the sum of the molar ratios of the inner and outer leaflets), were characterized before and after bet

295 aflet of the PM, but PS redistributes to the outer leaflet when the cell is damaged or at the onset o

296 osis, these phospholipids move to the cell's outer leaflet where they are recognized by so-called PS

297 tor activation, PM sterol was shifted to the outer leaflet, where it could be removed by HDL.

298 d to extract phospholipids from the membrane outer leaflet, while delivering lipids to the cell to ma

299 the most abundant phospholipids in the RBCs outer leaflet with PC 34:1 and SM 34:1 being the most ab

300 ich show restricted diffusion of IMPs of the outer leaflet, with our simulations, we conjectured the