ライフサイエンスコーパス: unilamellar vesicle

1 igand): soluble and anchored to a LUV (large unilamellar vesicle).

2 tube) membrane and a pipette-aspirated giant unilamellar vesicle.

3 h their interactions in monolayers and giant unilamellar vesicles.

4 e stabilization and leakage on diverse small unilamellar vesicles.

5 r detergent-mediated reconstitution in large unilamellar vesicles.

6 d membranes that self-assemble to form small unilamellar vesicles.

7 r of these membrane-active peptides in giant unilamellar vesicles.

8 te into liposomes and form channels in large unilamellar vesicles.

9 and phosphatidylserine in the form of large unilamellar vesicles.

10 omain on tubular membranes pulled from giant unilamellar vesicles.

11 limited leakage of a fluorophore from small unilamellar vesicles.

12 ized in the liquid disordered phase in giant unilamellar vesicles.

13 bly sites, using purified proteins and giant unilamellar vesicles.

14 mers in phosphatidylcholine-containing large unilamellar vesicles.

15 consistent with the effect of LL-37 on giant unilamellar vesicles.

16 anes and essentially flat membranes of giant unilamellar vesicles.

17 motions for these molecules in a variety of unilamellar vesicles.

18 ors of one-, two-, and three-component large unilamellar vesicles.

19 nfluence of these two steroids on DPPC large unilamellar vesicles.

20 r and deform plasma membrane-mimicking giant unilamellar vesicles.

21 icles of 1:1:1 DOPC/DPPC/sterol within giant unilamellar vesicles.

22 face area fraction of ordered phase in giant unilamellar vesicles.

23 Texas Red MARCKS(151-175) adsorbed to large unilamellar vesicles.

24 uring polymer-induced dye leakage from large unilamellar vesicles.

25 different methods applied to giant and large unilamellar vesicles.

26 aggregates induced vesicle budding in giant unilamellar vesicles.

27 ncrease that temperature when added to giant unilamellar vesicles.

28 lifetime imaging microscopy (FLIM) on giant unilamellar vesicles.

29 ting of proteins to lipid membranes of giant unilamellar vesicles.

30 n studied as transmembrane anion carriers in unilamellar vesicles.

31 haSyn inhibits the fusion of synthetic small unilamellar vesicles.

32 00 nm liposomes and modest effect with giant unilamellar vesicles.

33 microscopy were used to reveal that they are unilamellar vesicles.

34 measure thermal shape fluctuations in giant unilamellar vesicles.

35 d directly visualized Drp1 activity in giant unilamellar vesicles.

36 In two-component phosphatidylcholine unilamellar vesicles [1,2-dioleoyl-sn-glycero-3-phosphoc

37 molecule was observed to assemble into large unilamellar vesicles (350 nm, TEM) in water and thereby

38 m of sphingosine efflux from large and giant unilamellar vesicles; a graded-release efflux has been d

39 Using giant unilamellar vesicles able to separate into two coexistin

40 Model membrane systems, including giant unilamellar vesicles, allow optical fluorescence discrim

41 e observed time behavior of individual giant unilamellar vesicles, although complex, exhibited the ph

42 Histone binding to giant unilamellar vesicle and vesicle aggregation was visualiz

43 hanges due to lipid transfer between anionic unilamellar vesicles and a cationic supported bilayer we

44 erlin change the lipid packing of both small unilamellar vesicles and giant plasma membrane vesicles.

45 In vitro studies using small unilamellar vesicles and giant unilamellar vesicles demo

46 two-photon fluorescence polarimetry in giant unilamellar vesicles and in the plasma membrane (PM) of

47 terbium-dipicolinic acid complex from large unilamellar vesicles and migrated as a trimer by blue-na

48 In large unilamellar vesicles and monocyte cells, we showed that

49 nt analogues with large and cell-sized giant unilamellar vesicles and supported bilayers are reported

50 than the D in the outer leaflet or in giant unilamellar vesicles and the diffusion coefficient for o

51 ally reconstituted the ATP synthase in giant unilamellar vesicles and tracked the membrane fluctuatio

52 S in two phospholipid membrane models: giant unilamellar vesicles and water-in-oil droplet monolayers

53 (verified by comparison to results for giant unilamellar vesicles) and accurately quantify the dramat

54 c helix is sufficient for budding into giant unilamellar vesicles, and mutation of this sequence inhi

55 region were anchored to the surface of small unilamellar vesicles, and PrP-PrP interactions were moni

56 mixed bile salt micelles, phospholipid small unilamellar vesicles, and trioleoylglycerol emulsions wh

57 Giant unilamellar vesicles are a widely utilized model membran

58 Unilamellar vesicles are observed to form in aqueous sol

59 ayers, contours of these bilayers, and large unilamellar vesicles are shown.

60 the two proteins was determined using large unilamellar vesicles as a reaction surface.

61 was assessed with red blood cells and giant unilamellar vesicles as membrane models for endosomes.

62 GFP hemichannels were reconstituted in giant unilamellar vesicles as proven by fluorescence microscop

63 cture of the artificial channels using large unilamellar vesicle assays and the structural parameters

64 Unilamellar vesicles assembled layer-by-layer support fu

65 o investigated the effects of hIAPP on giant unilamellar vesicles at various peptide concentrations.

66 Using a novel giant unilamellar vesicle-based system, we found that PI(4,5)P

67 When small unilamellar vesicles bearing neuronal v-SNAREs fused wit

68 the size and changes the morphology of giant unilamellar vesicles by inducing massive vesiculation of

69 letal network formed on the surface of giant unilamellar vesicles by the prokaryotic tubulin homolog,

70 rs to phospholipid vesicles (small and large unilamellar vesicles) by a dual fluorescence approach th

71 by random diffusion or, in the case of large unilamellar vesicles, by microtubule-dependent transport

72 omplementary DNA-lipids, inserted into small unilamellar vesicles, can mediate membrane fusion in bul

73 We utilized micropipette aspiration of giant unilamellar vesicles composed of 1-stearoyl-2-oleoyl-pho

74 Giant unilamellar vesicles composed of a ternary mixture of ph

75 Using this new assay, we found that, in unilamellar vesicles composed of DHE and 1-palmitoyl-2-o

76 eglycol (PEG)-mediated fusion of 25 nm small unilamellar vesicles composed of dioleoylphosphatidylcho

77 hylene glycol)(PEG)-mediated fusion of small unilamellar vesicles composed of dioleoylphosphatidylcho

78 red lipid domains in a model system of giant unilamellar vesicles composed of dioleoylphosphatidylcho

79 ly(ethylene glycol)-mediated fusion of small unilamellar vesicles composed of dioleoylphosphatidylcho

80 or small (SUV), large (LUV), and giant (GUV) unilamellar vesicles composed of egg phosphatidylcholine

81 The release of carboxyfluorescein from large unilamellar vesicles composed of lipids characteristical

82 affinities of cholesterol oxidase to 100-nm unilamellar vesicles composed of mixtures of DOPC or DPP

83 n-scale liquid-liquid immiscibility in giant unilamellar vesicles composed of ternary mixtures of cho

84 The adsorption of large unilamellar vesicles composed of various combinations of

85 nd confocal fluorescence microscopy of giant unilamellar vesicles concurred in showing that equimolar

86 Microscopy studies in giant unilamellar vesicles confirmed that PFO exhibits interme

87 We reconstituted rhodopsin into large unilamellar vesicles consisting of polyunsaturated 18:0,

88 ed protein-coated membranes by forming giant unilamellar vesicles containing a small amount of biotin

89 rm an extended structure that bound to large unilamellar vesicles containing acidic phospholipids, pr

90 erol content also appeared in multicomponent unilamellar vesicles containing bovine brain sphingomyel

91 tive analysis of ANX partitioning into large unilamellar vesicles containing either 25% or 75% anioni

92 Large unilamellar vesicles containing extracts are produced in

93 Using reconstituted giant unilamellar vesicles containing preassembled t-SNARE pro

94 ucture rings to template uniform-sized small unilamellar vesicles containing predetermined maximal nu

95 ls the docking, priming, and fusion of small unilamellar vesicles containing the v-SNARE VAMP2 and th

96 vesicles (large unilamellar vesicle or small unilamellar vesicle) containing negatively charged phosp

97 t of purified AKAP18delta fragments to large unilamellar vesicles correlates (i) with the fraction of

98 ial membrane association or changes in large unilamellar vesicle curvature.

99 theronal A (1a) or atheronal B (1b) in large unilamellar vesicles (cyt-LUVs) with the lipid compositi

100 a from method 4 overlap and validate the new unilamellar vesicles data for DMPC, so method 4 is not r

101 ted membrane interfaces in vitro using giant unilamellar vesicles decorated with synthetic binding an

102 s using small unilamellar vesicles and giant unilamellar vesicles demonstrated that L-threo-LacCer di

103 elf-assembled into uniform, stable, and soft unilamellar vesicles, denoted glycodendrimersomes.

104 Unilamellar vesicles (diameter approximately 200 nm) for

105 Large unilamellar vesicles (diameter approximately 200 nm), a

106 ngly, whilst the use of 10% PEG in the small unilamellar vesicles did not block the formation of a de

107 he dynamics and fusogenicity of single large unilamellar vesicles doped with the v-SNARE synaptobrevi

108 We used giant unilamellar vesicles, each of which was aspirated in a m

109 iposomes and induces vesiculation into giant unilamellar vesicles, effects that are abrogated by hydr

110 was reconstituted and visualized using giant unilamellar vesicles, fluorescent ESCRT-0, -I, -II and -

111 RNA molecules inside 100- to 200-nm diameter unilamellar vesicles, following the procedures described

112 ilayers for q(z) extending to 0.85 A(-1) and unilamellar vesicles for smaller q(z).

113 Using giant unilamellar vesicles formed from a quaternary lipid mixt

114 Giant unilamellar vesicles formed from ACGal-containing mixtur

115 sensitive to the molar composition of large unilamellar vesicles formed from cholesterol, distearoyl

116 el were identified using lipid models (large unilamellar vesicles, giant unilamelllar vesicles, and l

117 icin (Hyp) from aqueous solutions into giant unilamellar vesicle (GUV) membranes has been studied exp

118 ed exterior of the resulting polymeric giant unilamellar vesicles (GUVs) allows their selective inter

119 compatible with multidomain imaging in giant unilamellar vesicles (GUVs) and cells by confocal laser

120 RE-mediated docking and fusion between giant unilamellar vesicles (GUVs) and smaller liposomes or pur

121 Giant unilamellar vesicles (GUVs) are convenient biomimetic sy

122 al studies showed that when cell-sized giant unilamellar vesicles (GUVs) are exposed to hypotonic med

123 Giant unilamellar vesicles (GUVs) are presumably the current m

124 artitioning in various lipid phases in giant unilamellar vesicles (GUVs) as a model system.

125 Specifically, we use giant unilamellar vesicles (GUVs) as soft colloids and explore

126 ures below Tmix in GPMVs as well as in giant unilamellar vesicles (GUVs) composed of ternary mixtures

127 oxidation, large rafts did not form in giant unilamellar vesicles (GUVs) containing 20 or more mol %

128 of membrane shape, we used cell-sized giant unilamellar vesicles (GUVs) containing either the potass

129 order, we measured protein binding to giant unilamellar vesicles (GUVs) containing the same PS conce

130 Giant unilamellar vesicles (GUVs) have been widely used as a m

131 e study the behavior of multicomponent giant unilamellar vesicles (GUVs) in the presence of AzoTAB, a

132 ping, holding, and rotating individual giant unilamellar vesicles (GUVs) inside dielectrophoretic mic

133 Liquid-liquid phase separation in giant unilamellar vesicles (GUVs) leads to the formation of in

134 ed tubulin binding to the membranes of giant unilamellar vesicles (GUVs) made from DOPC and DOPC/DOPE

135 and fluorescence microscopy to observe giant unilamellar vesicles (GUVs) made of erythrocyte membrane

136 sphosphate (PI(4,5)P2)-rich domains in giant unilamellar vesicles (GUVs) of complex lipid composition

137 Giant unilamellar vesicles (GUVs) of identical composition to

138 ype of gel-liquid phase segregation in giant unilamellar vesicles (GUVs) of mixed lipids.

139 scanning calorimetry was performed on giant unilamellar vesicles (GUVs) of pure dipalmitoylphosphati

140 to the membrane than those measured at giant unilamellar vesicles (GUVs) or a plane glass interface.

141 In samples of giant unilamellar vesicles (GUVs) prepared by electroformation

142 ing-disk confocal microscopy (SDCM) of giant unilamellar vesicles (GUVs) that allow for the detailed

143 shed a bilayer system based on adhered giant unilamellar vesicles (GUVs) to be able to control and ad

144 In this study, we used giant unilamellar vesicles (GUVs) to examine how PI(4,5)P2 wit

145 ermeability in E. coli spheroplasts or giant unilamellar vesicles (GUVs) under well-defined concentra

146 ed lipid bilayers (SLBs) on glass from giant unilamellar vesicles (GUVs) was studied using fluorescen

147 ncorporated into the lipid membrane of giant unilamellar vesicles (GUVs) whose dimensions match those

148 Cell-sized giant unilamellar vesicles (GUVs) would be ideal for in vitro

149 luorescence-microscopy image stacks of giant unilamellar vesicles (GUVs), a dedicated 3D-image analys

150 The method employs giant unilamellar vesicles (GUVs), which are 20-60 mum in diam

151 uid phase morphologies are observed on giant unilamellar vesicles (GUVs).

152 ple method to obtain stable asymmetric giant unilamellar vesicles (GUVs).

153 dy reported drastic effects of EGCg on giant unilamellar vesicles (GUVs).

154 lcholine or DEPC) on the morphology of giant unilamellar vesicles (GUVs, used as a biomembrane model)

155 of the diester phosphate of phospholipids in unilamellar vesicles has been studied from 0.004 to 11.7

156 Fluorescence microscopy imaging of giant unilamellar vesicles has greatly assisted the determinat

157 Individual unilamellar vesicles have been isolated using laser twee

158 is observed on the surface of ternary giant unilamellar vesicles held in a temperature gradient in c

159 s with a higher affinity than it bound large unilamellar vesicles in stopped-flow measurements.

160 ron microscopy (TEM) confirm the presence of unilamellar vesicles in the corresponding solutions.

161 tructural and mechanical properties of small unilamellar vesicles in the fluid-phase.

162 asket 1, forming a curved monolayer of large unilamellar vesicles in water (CAC < 0.25 muM), and biva

163 ,3,6-trisulfonic acid) encapsulated in large unilamellar vesicles in which the channel of interest ha

164 equilibrium dissociation constant for small unilamellar vesicles increases more than 50 times ( appr

165 e to show that the presence of anionic small unilamellar vesicles inhibits amyloid fibril formation b

166 AMO-induced topological transition of small unilamellar vesicles into an inverted hexagonal phase, i

167 behavior, leading to the conversion of large unilamellar vesicles into highly curved vesicles approxi

168 ndent oligomerization that transformed giant unilamellar vesicles into small vesicles connected throu

169 , showing that enterocyte microvilli release unilamellar vesicles into the intestinal lumen; these ve

170 opensity to induce membrane tubules in giant unilamellar vesicles is more pronounced for Gb3-S.

171 xternal side of cardiolipin-containing giant unilamellar vesicles, leads to the formation of tubules

172 ant EspD spontaneously integrates into large unilamellar vesicle (LUV) lipid bilayers; however, pore

173 oyl-Sn-glycero-3-phosphocholine (POPC) large unilamellar vesicle (LUV) model biomembrane system was s

174 sucrose density gradients reveals that large unilamellar vesicles (LUV) and sedimented multilamellar

175 t established an in vitro assay method using unilamellar vesicles (LUV) of deuterium-labeled substrat

176 Large unilamellar vesicles (LUV) prepared from the polar lipid

177 ngly partitioned into the membranes of large unilamellar vesicles (LUV), adopting a beta-sheet struct

178 amined two ways to bind the protein to large unilamellar vesicles (LUV).

179 ated with the main phase transition of large unilamellar vesicles (LUVs) and multilamellar vesicles (

180 e IQ domains and bound calmodulins) to large unilamellar vesicles (LUVs) composed of phosphatidylchol

181 t, CdtB, also is capable of binding to large unilamellar vesicles (LUVs) containing cholesterol.

182 d that the myo1e tail binds tightly to large unilamellar vesicles (LUVs) containing physiological con

183 he outer membrane phospholipase A into large unilamellar vesicles (LUVs) of 1,2-dilauroyl-sn-glycero-

184 d relative volume fluctuations of PLFE large unilamellar vesicles (LUVs) over a wide range of tempera

185 dimyristoylphosphatidylcholine (DMPC) large unilamellar vesicles (LUVs) were incubated with apolipop

186 We purified and reconstituted IAR into large unilamellar vesicles (LUVs), and demonstrated the proton

187 nge-based method to prepare asymmetric large unilamellar vesicles (LUVs), which have less membrane cu

188 e standards, lipid droplets (LDs), and large unilamellar vesicles (LUVs).

189 (IQ-tail)) to and from 100-nm diameter large unilamellar vesicles (LUVs).

190 purified ACR protein reconstituted in large unilamellar vesicles (LUVs).

191 etic membranes that are assembled into large unilamellar vesicles (LUVs).

192 -oleoylphosphatidylcholine/cholesterol large unilamellar vesicles (LUVs).

193 oyl-l-alpha-phosphatidylcholine (POPC) large unilamellar vesicles (LUVs, approximately 800 nm in diam

194 We performed kinetic experiments using giant unilamellar vesicles made of 7:3 DOPC/DOPG.

195 us solubilization of either multilamellar or unilamellar vesicles made of a membrane-PL mixture and F

196 ions of the local anesthetic tetracaine with unilamellar vesicles made of dimyristoyl or dipalmitoyl

197 Confocal experiments on giant unilamellar vesicles made of human, sheep, and rabbit er

198 e alphaS helix triggers an increase in small unilamellar vesicle membrane leakage.

199 umber of conducting gA channels in the large unilamellar vesicle membrane, will be detectable as chan

200 Myr-Gag forms clusters on giant unilamellar vesicle membranes containing the plasma memb

201 nalysis of the photodamage promoted on giant unilamellar vesicles membranes made of dioleoyl-sn-glyce

202 A14.1, TW-37) in biochemically defined large unilamellar vesicle model systems that faithfully recapi

203 cyt c crossing the membrane barrier of giant unilamellar vesicle model systems, we investigate the in

204 ents and coarse-grained simulations on giant unilamellar vesicles of 1,2-dipalmitoyl-sn-glycero-3-pho

205 NMR study in which alphaS is added to small unilamellar vesicles of a composition mimicking synaptic

206 Confocal fluorescence microscopy of giant unilamellar vesicles of all of the compositions under st

207 Unilamellar vesicles of an equimolar mixture of dimyrist

208 tering was measured from oriented stacks and unilamellar vesicles of dioleoylphosphatidylcholine lipi

209 nding, as measured by turbidity clearance of unilamellar vesicles of DMPC, is faster at acidic pH val

210 se patterned surfaces to a solution of small unilamellar vesicles of phospholipids and their mixtures

211 e analysis of the binding of alphaS to large unilamellar vesicles of various lipid compositions.

212 Unilamellar vesicles of varying net charge and lipid com

213 mbrane junctions, formed by rupture of giant unilamellar vesicles onto conventional supported lipid m

214 ation of phosphatidylcholine vesicles (large unilamellar vesicle or small unilamellar vesicle) contai

215 Giant unilamellar vesicles or GUVs are systems of choice as bi

216 intrinsic curvature and thereby stress small unilamellar vesicle outer leaflets as well as the periph

217 th a >15-fold increase in affinity for small unilamellar vesicles over large unilamellar vesicles, su

218 easurements of influx rates in SUV and giant unilamellar vesicles performed with oleate-BSA complexes

219 yoctecadienoate esters of 2-lyso-PC in small unilamellar vesicles produced the 9-hydroxy-12-oxododec-

220 show that reconstitution of opsin into large unilamellar vesicles promotes rapid (tau<10 s) flipping

221 now show that when reconstituted into large unilamellar vesicles, purified BR trimers exhibit light-

222 cence microscopy show that AMO-treated giant unilamellar vesicles remain intact, instead of reconstru

223 thers pulled from micropipet-aspirated giant unilamellar vesicles, repartitioning of membrane-bound E

224 mains, efficiently bent the surface of large unilamellar vesicles, resulting in the formation of tubu

225 Fluorescence polarization studies of small unilamellar vesicles revealed that hopanoid 2-methylatio

226 vitro experiments with Gb3-containing giant unilamellar vesicles revealed that LecA/Gb3-mediated lip

227 Dendrimersomes are stable, monodisperse unilamellar vesicles self-assembled in water from amphip

228 rescence microscopy measurements using giant unilamellar vesicles showed that A2t of wild type, but n

229 Fluorescence microscopy of giant unilamellar vesicles shows micrometer-scale domains belo

230 adiating methylene blue present in the giant unilamellar vesicles solution.

231 these peptide-induced perturbations in giant unilamellar vesicles, suggesting size-dependent membrane

232 ty for small unilamellar vesicles over large unilamellar vesicles, suggesting that alphaS may be a cu

233 h their ability to induce leakage from large unilamellar vesicles, supporting membrane permeabilizati

234 ed-flow mixing of uncomplexed FFA with small unilamellar vesicles (SUV) containing pyranine yields th

235 Because these studies have focused on small unilamellar vesicles (SUV), they leave open the question

236 nerated upon binding to LEM and egg PC small unilamellar vesicles (SUV).

237 inding to egg phosphatidylcholine (PC) small unilamellar vesicles (SUV).

238 low curvature stress, i.e., small and large unilamellar vesicles (SUVs and LUVs).

239 association, we reacted N-62 StAR with small unilamellar vesicles (SUVs) composed of lipids resemblin

240 BV interacted directly with small unilamellar vesicles (SUVs) comprised of phospholipids p

241 sn-glycero-3-[phospho-L-serine] (DOPS) small unilamellar vesicles (SUVs) dramatically enhances the ag

242 -free apolipoprotein A-I (apoA-I) with small unilamellar vesicles (SUVs) of 1-palmitoyl, 2-oleoyl pho

243 -free apolipoprotein A-I (apoA-I) with small unilamellar vesicles (SUVs) of 1-palmitoyl-2-oleoylphosp

244 nstrate that peptide binding to either small unilamellar vesicles (SUVs) or bicelles can readily be d

245 DMPC in the form of small unilamellar vesicles (SUVs) or DMPC-NP-SLBs with excess

246 lowing triple homologous immunisation, small unilamellar vesicles (SUVs) with no TLR agonists showed

247 bution studies, it was found that with small unilamellar vesicles (SUVs), 10% PEGylation of the formu

248 On analogous small unilamellar vesicles (SUVs), the conformation of alphaS

249 diated eNOS activation by both HDL and small unilamellar vesicles (SUVs), whereas the SR-BI mutant AV

250 re biological membrane-like asymmetric small unilamellar vesicles (SUVs).

251 ly binds to ganglioside GM1-containing small unilamellar vesicles (SUVs).

252 orescently labeled proteins on PC-rich small unilamellar vesicles (SUVs).

253 acteria to transport small, large, and giant unilamellar vesicles (SUVs, LUVs, and GUVs).

254 iant unilamellar vesicles with that of giant unilamellar vesicles that contain phosphatidylglycerol (

255 nts were done using fluorophore-loaded large unilamellar vesicles that had been doped with gA, and ch

256 he transition temperature in GPMVs and giant unilamellar vesicles that results from the addition of a

257 In giant unilamellar vesicles the change in temperature displays

258 , compared with cardiolipin-containing giant unilamellar vesicles the tubules are longer, exhibit a v

259 non-substrate membrane model systems (small unilamellar vesicle) through its N-terminal domain, indu

260 ental setup for modulating adhesion of giant unilamellar vesicles to a planar substrate.

261 ve utilized micropipette aspiration of giant unilamellar vesicles to determine salicylate's effects o

262 Here, we microaspirate giant unilamellar vesicles to determine the effect of mechanic

263 We used unilamellar vesicles to explore the effects of PFCs on m

264 rified RNAs, recombinant HIV-1 Gag and giant unilamellar vesicles to recapitulate the selective packa

265 Experiments performed on model giant unilamellar vesicles under a confocal laser scanning mic

266 formation is modeled on the surface of giant unilamellar vesicles using a Landau field theory model f

267 G protein coupled receptor 5-HT1A into giant unilamellar vesicles using an agarose rehydration method

268 in dodecylphosphocholine micelles and small unilamellar vesicles using circular dichroism spectrosco

269 escently labeled Lipid II molecules in giant unilamellar vesicles using light-sheet illumination.

270 Confocal microscopy of intact giant unilamellar vesicles verified that in the absence of GAP

271 scission of intralumenal vesicles into giant unilamellar vesicles was reconstituted and visualized by

272 pectroscopy to VDAC reconstituted into giant unilamellar vesicles, we demonstrate that PG significant

273 Using micropipette manipulation of giant unilamellar vesicles, we directly measured the lysis ten

274 erbium-dipicolinic acid complex-loaded large unilamellar vesicles, we found that TP0453 increased eff

275 Using giant unilamellar vesicles, we show that pUL31 and pUL34 are s

276 nt apical membranes reconstituted into giant unilamellar vesicles, we showed a 2-fold decrease in lat

277 Using giant unilamellar vesicles, we visualized the formation of wri

278 detect quenching of Bodipy-TMR-PIP2 in large unilamellar vesicles when unlabeled MARCKS(151-175) bind

279 we study the mechanics of liposomes or giant unilamellar vesicles, when a biomimetic actin cortex is

280 to generate highly monodispersed sub-100-nm unilamellar vesicles, where liposome self-assembly was n

281 se were verified by domain behavior in giant unilamellar vesicles, which displayed two-dimensional mi

282 can insert into the lipid bilayer of a small unilamellar vesicle, while the other spans a planar lipi

283 ely 13 nm diameter domains residing in 60 nm unilamellar vesicles, whose lipid composition mimics the

284 Hsv2 bound small unilamellar vesicles with a higher affinity than it boun

285 It enables the spontaneous creation of unilamellar vesicles with a narrow size distribution tha

286 n microscopy of exosomes, we found spherical unilamellar vesicles with a significant protein content,

287 PPDHQ to image the phase separation in giant unilamellar vesicles with both linear and nonlinear opti

288 activity by human and rat PITPs, using small unilamellar vesicles with carefully controlled phospholi

289 d phase coexistence to the geometry of giant unilamellar vesicles with coexisting liquid-disordered (

290 changes (multilayering) upon aggregation of unilamellar vesicles with concanavalin A.

291 3), X-ray scattering from extruded unilamellar vesicles with diameter 600 A provided |F(q(z

292 ains within membranes of free-floating giant unilamellar vesicles with diameters between 80 and 250 m

293 in a model of viral egress we employed giant unilamellar vesicles with different lipid compositions.

294 onomer exhibits a reduced affinity for small unilamellar vesicles with lipid composition similar to s

295 esent an integrated method for forming giant unilamellar vesicles with simultaneous control over (i)

296 hange technique was devised to prepare small unilamellar vesicles with stable asymmetric lipid compos

297 are the case of cardiolipin-containing giant unilamellar vesicles with that of giant unilamellar vesi

298 By correlating experiments using giant unilamellar vesicles with those of peptide-lipid multila

299 e the size of nanoscopic membrane domains in unilamellar vesicles with unprecedented accuracy.

300 protein integration directly into preformed unilamellar vesicles without the use of surfactants.