ライフサイエンスコーパス: membrane vesicle

1 ipid envelope, internal lipid core, or inner membrane vesicle.

2 ks the initial emergence of a protein-coated membrane vesicle.

3 nization and stability of MHV-induced double-membrane vesicles.

4 reagents to catalyze cross-link formation in membrane vesicles.

5 stituting them in vitro using inverted inner membrane vesicles.

6 etected after treatment with PPAD-null outer membrane vesicles.

7 rt of fatty acids by Tet38 was determined in membrane vesicles.

8 ted transport of Hoechst 33 342 dye in Tet38 membrane vesicles.

9 e vaccinology) combined with bacterial outer-membrane vesicles.

10 ultiple avenues, including lysis-independent membrane vesicles.

11 1) protein natively anchored in cell-derived membrane vesicles.

12 cause 1 collapsed the proton motive force in membrane vesicles.

13 e in detergent solution and in reconstituted membrane vesicles.

14 preciated source of bioactive, extracellular membrane vesicles.

15 I secretion (T3SS) apparati as well as outer membrane vesicles.

16 small unilamellar vesicles and giant plasma membrane vesicles.

17 d in their native environment of cytoplasmic membrane vesicles.

18 structures are represented mostly by double-membrane vesicles.

19 MaX1 catalyzes Ca(2+) uptake into membrane vesicles.

20 cellular membranes such as single- or double-membrane vesicles.

21 y a role in thylakoid membrane formation via membrane vesicles.

22 to the B. henselae outer membrane and outer membrane vesicles.

23 p11 and show increased fusion of perinuclear membrane vesicles.

24 nuated the binding of palmitoylated PFK-1 to membrane vesicles.

25 purified lipopolysaccharide (LPS) and outer membrane vesicles.

26 ignols and their derivatives by these native membrane vesicles.

27 H(+) transport was measured using inside-out membrane vesicles.

28 using a protease protection assay in sealed membrane vesicles.

29 e cytosol (uncoated) from those still within membrane vesicles.

30 e surfaces of A431 cancer cells and isolated membrane vesicles.

31 acteria, with a thick cell wall, can release membrane vesicles.

32 p66 are constituents of B. burgdorferi outer membrane vesicles.

33 nner consistent with the production of outer membrane vesicles.

34 bending) proteins, pili, flagella, and outer membrane vesicles.

35 Exosomes are small membrane vesicles (30-100nm in diameter) secreted by cel

36 transport by probenecid in renal basolateral membrane vesicles (5.2-fold).

37 Blood microparticles (MPs) are small membrane vesicles (50-1000nm), derived from different ce

38 Exosomes are nano-sized membrane vesicles (50-120 nm), which are released from a

39 4 was present in HSC exosomes, which were bi-membrane vesicles, 50-150 nm in diameter, negatively cha

40 at when applied to cell-derived giant plasma membrane vesicles, a variant of CTxB containing only a s

41 e found in mouse plasma that cBIN1 exists in membrane vesicles about 200 nm in size, which is consist

42 c goods transported extracellularly in outer membrane vesicles allowing for the creation of PBP and c

43 (2+) signals and actively traffic GFP-tagged membrane vesicles along their length.

44 cal serogroup B vaccine (4CMenB) is an outer membrane vesicle and recombinant protein-based vaccine l

45 These structures, including double-membrane vesicles and convoluted membranes, are linked,

46 is is connected with the formation of double-membrane vesicles and convoluted membranes.

47 plasmic components are sequestered in double-membrane vesicles and degraded on fusion with lysosomal

48 nduced upon CVB3 infection, such as compound membrane vesicles and highly geometric paracrystalline a

49 ate transport in isolated renal brush border membrane vesicles and in cultured renal proximal tubule

50 In membrane vesicles and in intact cells, the coproduction

51 esolve RyR2 CaM binding, both in isolated SR membrane vesicles and in permeabilized ventricular myocy

52 Lactococcus lactis and studied in inside-out membrane vesicles and in purified form.

53 d BSAP-1, is secreted from the cell in outer membrane vesicles and no additional proteins are require

54 observed in human blood represent non-living membrane vesicles and protein aggregates derived from bl

55 g," a method for rapid proteomic analysis of membrane vesicles and protein particles.

56 as been probed by varying the solvent within membrane vesicles and proteoliposomes.

57 ontrast, phosphate transport in brush border membrane vesicles and proximal tubule cells from sodium-

58 that ultimately result in the production of membrane vesicles and release of the acrosomal contents.

59 ribosomes with the SecYEG complex present in membrane vesicles and the purified SecYEG complex presen

60 investigation regarding these extracellular membrane vesicles and their potential in diagnostic and

61 esence of protein Z (PZ), negatively charged membrane vesicles, and calcium ions approached the same

62 , receptors, large macromolecular complexes, membrane vesicles, and exosomes that can modify the micr

63 ATP hydrolysis and ion transport in inverted membrane vesicles, and experimentally demonstrate that t

64 ort measurements in intact cells, inside-out membrane vesicles, and proteoliposomes containing functi

65 istae tips dissociate into monomers in inner-membrane vesicles, and the membrane curvature at the ATP

66 Endocytosis generates double-membrane vesicles (annular GJs or connexosomes) in the c

67 M. tuberculosis), we propose that bacterial membrane vesicles are secreted by M. tuberculosis within

68 Our findings suggest that bacterial membrane vesicles are the primary means by which M. tube

69 with the viral glycoproteins) encased within membrane vesicles are transported in the anterograde dir

70 Exosomes, nano-sized membrane vesicles, are released by various cells and are

71 found for full-length YehU in right-side-out membrane vesicles as well as for a truncated, membrane-i

72 ENTH-bound membrane morphologies, including membrane vesicles as well as preformed membrane tubules.

73 ts, on ATP synthesis by ADP- and P(i)-loaded membrane vesicles at pH 7.5 and 10.5.

74 tosolic constituents are enveloped by double-membrane vesicles, autophagosomes, which later fuse with

75 rization by western blots using brush border membrane vesicles (BBMV) from a strain of P. xylostella

76 N2ta blocked Cry11Ba binding to brush border membrane vesicles (BBMV) of A. gambiae whereas the toxic

77 on western corn rootworm midgut brush border membrane vesicles (BBMV).

78 ts by regulating the quantity of Mtb-derived membrane vesicles bearing Toll-like receptor 2 ligands,

79 The trafficking of membrane vesicles between different intracellular organe

80 n assays with aphid gut-derived brush border membrane vesicles, binding of CP-P-GFP competed with bin

81 poliovirus, which also replicates in double-membrane vesicles, but not for dengue virus, which repli

82 in isolated, cytoskeleton-free giant plasma membrane vesicles, but not in intact cell membranes.

83 ced rearrangements such as single- or double-membrane vesicles, but the mechanisms of such rearrangem

84 ace gangliosides, allowing engulfment into a membrane vesicle by a clathrin-independent process.

85 Coassembly with the components of bacterial membrane vesicles by a dehydration-rehydration process g

86 bacterial virulence factor secreted in outer membrane vesicles by Pseudomonas aeruginosa, increases t

87 tegration and packaging of its contents into membrane vesicles called apoptotic bodies.

88 that sequesters cytosolic material in double membrane vesicles called autophagosomes and degrades it

89 ess characterized by the formation of double membrane vesicles called autophagosomes.

90 rt that during traumatic brain injury, small membrane vesicles, called microparticles, disseminate pr

91 ter membrane extensions in the form of outer membrane vesicle chains and membrane tubes that intercon

92 confirmed in cultured cells and in cell-free membrane vesicles characterized by acute inhibition of t

93 of both LPS and protein components of outer membrane vesicles combine to produce a bacterial strain-

94 in the polysialyltransferase produces outer membrane vesicles containing an acceptor for the alpha-2

95 nce resonance energy transfer assay in model membrane vesicles containing coexisting ordered and diso

96 h antibiotic susceptibility and formation of membrane vesicles containing greater amounts of vaccine

97 as effective in activating kinase as native membrane vesicles containing many neighbouring dimers.

98 e hypothesize that exosomes, which are small membrane vesicles containing mycobacterial components re

99 SN are membrane vesicles containing pre- and post-synaptic comp

100 w that the bacteria-like entities consist of membrane vesicles containing serum and exosome proteins,

101 We also propose that outer membrane vesicle-containing meningococcal vaccines may b

102 stinct subcellular structures such as double-membrane vesicles, convoluted membranes, and tubular str

103 genic plasminogen receptor released in outer membrane vesicles could be responsible for external prot

104 ependent phosphate transport in brush border membrane vesicles derived from hormone-treated kidney sl

105 tracellular vesicles (EVs) are small, double membrane vesicles derived from leukocytes, platelets, an

106 Instead, outer membrane vesicles derived from N. lactamica mediate a B

107 capsulation of drugs via remote loading into membrane vesicles derived from red blood cells.

108 irus-induced membrane changes include double-membrane vesicles (DMVs) and convoluted membranes.

109 addition to the conserved coronavirus double membrane vesicles (DMVs), Beau-R, an apathogenic strain

110 Coronaviruses induce double-membrane vesicles (DMVs), but the role of DMVs in replic

111 of exosomes and possibly other extracellular membrane vesicles (EMVs).

112 lls (OKF6) showed that they actively secrete membrane vesicles (exosomes) that are enriched with miR-

113 In everted membrane vesicles expressing CgAcr3-1, dissipation of ei

114 Although cell lysis and outer-membrane vesicle extrusion are possible means by which t

115 poration of cellular material into cytosolic membrane vesicles for lysosomal degradation.

116 esis, repair of the plasma membrane, nuclear membrane vesicle formation, and HIV budding.

117 to initiate recruitment of coat proteins for membrane vesicle formation.

118 Everted membrane vesicles from cells expressing arsJ accumulated

119 at natively express AQP1, in hemoglobin-free membrane vesicles from rat and human erythrocytes, and i

120 The release of membrane vesicles from the surface of cells into their s

121 Everted membrane vesicles from those cells accumulated MAs(III)

122 Acr3-1 was also the most active when everted membranes vesicles from Escherichia coli or C. glutamicu

123 ision in which a large number of TGN-derived membrane vesicles fuse with one another to form the part

124 vaccine consisting of glycoengineered outer membrane vesicles (geOMVs).

125 Escherichia coli to yield glycosylated outer membrane vesicles (glycOMVs) decorated with pathogen-mim

126 we report experiments utilizing giant plasma membrane vesicles (GPMVs) to explore how membrane transi

127 In contrast, for cell-derived giant plasma membrane vesicles (GPMVs), breaking the patch membrane a

128 ition temperature when added to giant plasma membrane vesicles (GPMVs), but increase that temperature

129 point observed in cell-derived giant plasma membrane vesicles (GPMVs).

130 cytoskeleton-free, cell-derived giant plasma membrane vesicles (GPMVs).

131 -alcohols are incorporated into giant plasma membrane vesicles (GPMVs).

132 se inhibitors, both WT- and SF-MRP1-enriched membrane vesicles had a high Km value for As(GS)3 (3-6 m

133 ments in human placental microvillous plasma membrane vesicles have persistently produced results tha

134 econstituted proteoliposomes and cytoplasmic membrane vesicles have revealed that the number of SecYE

135 ocess used to merge the synthetic and native membrane vesicles; importantly it was also conserved in

136 g identification of a highly active inverted membrane vesicle (IMV) fraction yielding transport rates

137 and VI are antagonistic motors that cohabit membrane vesicles in cells.

138 red to revertant virus, the number of double-membrane vesicles in MHV-Brts31-infected cells is reduce

139 mplexes are the predominant coat proteins of membrane vesicles in post-Golgi trafficking of mammalian

140 id substrates into isolated placental plasma membrane vesicles in the absence of opposing side amino

141 enhanced the formation and acidification of membrane vesicles in the cytoplasm.

142 Measurements on cell-derived membrane vesicles, in the plasma membrane of live cells,

143 Recently, actively secreted membrane vesicles, including exosomes, are being recogni

144 evidence indicates there is a role for small membrane vesicles, including exosomes, as vehicles for i

145 amics in individual CmeB trimers embedded in membrane vesicles indicates that each CmeB subunit under

146 inhibit lactose transport in right-side-out membrane vesicles, indicating that the Nbs recognize epi

147 o populations of PA pores were visualized in membranes, vesicle-inserted and nanodisc-inserted, allow

148 The shedding of these proteins by membrane vesicles into the medium is minimal.

149 ctures, some of which were similar to double membrane vesicles involved in virus replication.

150 However, enolase in the outer membrane vesicles is accessible to proteolytic degradati

151 ome from the phagophore, a cup-shaped double-membrane vesicle, is a critical step in autophagy.

152 irus-modified membrane structure, the double-membrane vesicle, is proportional to the rate of viral R

153 om rat and human erythrocytes, and in plasma membrane vesicles isolated from AQP1-transfected Chinese

154 ble adhesion zone is also observed in plasma membrane vesicles isolated from living RBL-2H3 cells, an

155 nteractions between these proteins in native membrane vesicles isolated from rabbit kidney.

156 ion of PINEM on whole human cancer cells and membrane vesicles isolated from them is reported.

157 athway for transporting cargo into cells via membrane vesicles; it plays an integral role in nutrient

158 onded to dense cell surface accumulations of membrane vesicle-like structures and were not fibrillar.

159 In vitro reconstitution of membrane vesicles loaded with prenylated Rac1 demonstrat

160 Previously unidentified membrane vesicles lying immediately beneath the plasma m

161 asure for GpATM in bilayers indicates that a membrane vesicle many orders of magnitude larger than a

162 Water flux across renal cortical membrane vesicles, measured by stopped-flow light scatte

163 In right-side-out membrane vesicles, melibiose efflux is inhibited by an i

164 assessed vaccine effectiveness of the outer membrane vesicle meningococcal B vaccine (MeNZB) against

165 ul, but surveillance data suggest that outer membrane vesicle meningococcal group B vaccines affect t

166 ylori facilitates bacterial persistence, and membrane vesicles (MV), which have the potential to cros

167 The release of bioactive membrane vesicles (MVs) from the cell surface is conserv

168 Recent studies indicate that membrane vesicles (MVs) secreted by various cells are as

169 Bacteria release membrane vesicles (MVs) that play important roles in var

170 Bacteria naturally release membrane vesicles (MVs) under a variety of growth enviro

171 Further, after treatment of C5 with outer membrane vesicles naturally shed by P. gingivalis, we ob

172 Outer membrane vesicles of B. burgdorferi contain enolase, a g

173 king studies on the McjD dimer in inside-out membrane vesicles of E. coli confirmed the presence of t

174 e extracellular environment diverse types of membrane vesicles of endosomal and plasma membrane origi

175 hat Tat-dependent protein translocation into membrane vesicles of Escherichia coli is blocked by the

176 Exosomes are nanometric membrane vesicles of late endosomal origin released by m

177 Membrane vesicles of this kind, termed exosomes and ecto

178 sembles its replication complex on cytosolic membrane vesicles often clustered in a membranous web (M

179 ly different delivery mechanism is the outer membrane vesicle (OMV) which is composed of bacterial ou

180 An outer membrane vesicle (OMV)-based cholera vaccine is highly e

181 gative bacteria constitutively release outer membrane vesicles (OMV), which may function in the deliv

182 into the host cytoplasm via bacterial outer membrane vesicles (OMV).

183 utation led to increased production of outer membrane vesicles (OMV).

184 here that engineered Escherichia coli outer membrane vesicles (OMVs) are an easily purified vaccine-

185 Outer membrane vesicles (OMVs) are composed of outer membrane

186 Outer membrane vesicles (OMVs) are nanoscale proteoliposomes t

187 Outer membrane vesicles (OMVs) are produced by all Gram-negati

188 Bacteria can naturally secrete outer membrane vesicles (OMVs) as pathogenic factors, while th

189 ed by H3-T6SS and is incorporated into outer membrane vesicles (OMVs) by directly interacting with th

190 We analyzed the potential of outer membrane vesicles (OMVs) derived from the NOVC strain V:

191 Many bacterial pathogens utilize outer membrane vesicles (OMVs) for delivery of virulence facto

192 Furthermore, an increased capacity of outer membrane vesicles (OMVs) formation and release was also

193 To address this, we used outer membrane vesicles (OMVs) from pathogenic bacteria as a p

194 of lipopolysaccharide (LPS)-detoxified outer membrane vesicles (OMVs) from Salmonella enterica serova

195 Production and release of outer-membrane vesicles (OMVs) is known in many bacteria inclu

196 Outer membrane vesicles (OMVs) isolated from Salmonella Typhim

197 Outer membrane vesicles (OMVs) of Gram-negative bacteria have

198 of adult female mice with V. cholerae outer-membrane vesicles (OMVs) passively protects suckling mic

199 Outer membrane vesicles (OMVs) produced by Gram-negative bacte

200 Here, we identify outer membrane vesicles (OMVs) produced by Gram-negative bacte

201 Here, we illustrate that outer membrane vesicles (OMVs) released by F. succinogenes are

202 es a cocktail of virulence factors via outer membrane vesicles (OMVs) shed during growth.

203 Pseudomonas aeruginosa produces outer membrane vesicles (OMVs) that contain a number of secret

204 Gram-negative bacteria produce outer membrane vesicles (OMVs) that contain biologically activ

205 tors to infect host cells by secreting outer membrane vesicles (OMVs) that contain small molecules, p

206 localized to host immune cells through outer membrane vesicles (OMVs) that harbor bacterial sulfatase

207 t Bacteroides fragilis releases PSA in outer membrane vesicles (OMVs) that induce immunomodulatory ef

208 esion to NETs involved the shedding of outer membrane vesicles (OMVs) that outcompeted the cytotoxic

209 Gram-negative bacteria produce outer membrane vesicles (OMVs) that package and deliver protei

210 Opa was contained within meningococcal outer membrane vesicles (OMVs), compared to Opa-negative OMVs.

211 l in an oligomeric conformation within outer membrane vesicles (OMVs), our findings suggest ClyA form

212 ied to date have been shown to produce outer membrane vesicles (OMVs), which are budded, released sph

213 bacteria have the capacity to release outer membrane vesicles (OMVs), which are nano-sized bilayered

214 he diarrheal disease cholera, secretes outer membrane vesicles (OMVs).

215 bacteria have been observed to secrete outer membrane vesicles (OMVs).

216 olysaccharides, secreted proteins, and outer membrane vesicles (OMVs).

217 on system (T6SS), autotransporter, and outer membrane vesicles (OMVs).

218 ysis revealed its abundant presence in outer membrane vesicles (OMVs).

219 cules to immune cells via secretion of outer membrane vesicles (OMVs).

220 roteins of gram-negative bacteria from outer membrane vesicles (OMVs).

221 d by several names (membrane vesicles, outer membrane vesicles [OMVs], exosomes, shedding microvesicl

222 nts in Cys154 --> Gly LacY in right-side-out membrane vesicles or after solubilization and purificati

223 ingdoms of life and called by several names (membrane vesicles, outer membrane vesicles [OMVs], exoso

224 Mycobacterium tuberculosis releases membrane vesicles packed with molecules that can modulat

225 otility assays with purified DDB and BICD2's membrane vesicle partner, the GTPase Rab6a.

226 In the presence of ATP, the inverted plasma membrane vesicles preferentially take up monolignol agly

227 lture supernatant, outer membrane, and outer membrane vesicle preparations, suggesting that many anti

228 Using isolated plasma and vacuolar membrane vesicles prepared from Arabidopsis, together wi

229 kinetics were observed between MRP1-enriched membrane vesicles prepared from human embryonic kidney 2

230 exhibit an H(+)-pumping activity in inverted membrane vesicles prepared from recombinant Escherichia

231 Extracellular vesicles (EV) are small membrane vesicles produced by cells upon activation and

232 In these studies, we found that membrane vesicles produced by M. tuberculosis and releas

233 iciency did not have a significant effect on membrane vesicle production; however, the protein profil

234 EBV-positive B cells with OKF6 cell-derived membrane vesicles promoted reactivation.

235 n: LXR inactivation by NeoB disrupted double-membrane vesicles, putative sites of viral replication.

236 nactivation resulted in dispersion of double-membrane vesicles, putative viral replication sites.

237 t these activities derive from the bacterial membrane vesicles rather than exosomes.

238 icroparticles (MPs) are submicron-sized shed membrane vesicles released from activated or injured cel

239 Exosomes, membrane vesicles released from cells within the lung al

240 Microparticles are cell-derived membrane vesicles, relevant to a range of biological res

241 three-dimensional architecture of the double-membrane vesicles, representing the sites of dengue viru

242 However, exosomes--membrane vesicles secreted by many cells, including MSCs

243 We propose that membrane vesicles secreted by oral and tonsillar epithel

244 Here we show that membrane vesicles secreted from oral epithelial cells co

245 eover, we show that both plasma and vacuolar membrane vesicles selectively transport different forms

246 MPs are submicron membrane vesicles shed by compromised or activated cells

247 ectron tomography of phage 'infecting' outer membrane vesicles shows the tail needle contacting and i

248 sociated within distances relevant to plasma membrane-vesicle SNARE interactions.

249 embrane extensions are associated with outer membrane vesicles, structures ubiquitous in Gram-negativ

250 Further evidence from giant plasma membrane vesicles suggests that the presence of an intac

251 In plants, membrane vesicles targeted to the cell division plane fu

252 C membrane was coated onto the nanogel via a membrane vesicle templated in situ gelation process, whe

253 fficking events to generate a de novo double-membrane vesicle termed the autophagosome, which matures

254 is characterized by the formation of double-membrane vesicles termed autophagosomes engulfing the su

255 It uses double- or multiple-membrane vesicles termed autophagosomes to remove protei

256 increased the number of lysosomes and double membrane vesicles termed autophagosomes, and enhanced th

257 TF is released into the circulation on small-membrane vesicles termed microparticles (MPs).

258 e efficiently taken up into MATE2-containing membrane vesicles than are the parent glycosides.

259 micron-sized critical fluctuations in plasma membrane vesicles that are detached from their cortical

260 MPs are small membrane vesicles that are highly procoagulant.

261 Cells release nano-sized membrane vesicles that are involved in intercellular com

262 Microparticles (MPs) are small cell membrane vesicles that are released from cells during ap

263 Most secreted LT is associated with outer membrane vesicles that are rich in lipopolysaccharide.

264 C-derived exosomes (Dex) are nanometer-sized membrane vesicles that are secreted by the sentinel anti

265 gram-negative sepsis and was associated with membrane vesicles that co-sedimented with the exosomal f

266 Exosomes (EXOs) are secreted, nano-sized membrane vesicles that contain potent immunostimulatory

267 hagy, which involves the formation of double membrane vesicles that engulf proteins and organelles th

268 complex II (COPII) mediates formation of the membrane vesicles that export newly synthesised proteins

269 proteins are generally carried out in model membrane vesicles that lack lipid asymmetry.

270 bly of COPI into a cage-like lattice sculpts membrane vesicles that transport cargo from the Golgi ap

271 pression of a miR-200 family member produced membrane vesicles that were able to induce the lytic cas

272 nes, resulting in the accumulation of double-membraned vesicles that resemble cellular autophagosomes

273 estration of cellular contents into a double-membrane vesicle, the autophagosome.

274 ablished modes of secretion, including outer membrane vesicles, the type II secretion system, and the

275 tiated estradiol glucuronide into inside-out membrane vesicles, their affinity for and ability to sti

276 engulfs cytoplasmic components within double-membrane vesicles to allow their delivery to, and subseq

277 sted role for phosphoinositides in targeting membrane vesicles to apicoplasts.

278 hagy is a conserved process that uses double-membrane vesicles to deliver cytoplasmic contents to lys

279 ted lipids and POPC lipids) with native cell-membrane vesicles to generate hybrid vesicles which read

280 egulating actin polymerization, transporting membrane vesicles to the leading edge, and/or facilitati

281 thetaiotaomicron are required for its outer membrane vesicles to transit to underlying host immune c

282 nexin A2, an RNA-binding protein involved in membrane vesicle trafficking, and is suppressed by exoso

283 and collectrin, which is involved in apical membrane vesicle trafficking.

284 rane-cytoskeletal interactions important for membrane/vesicle trafficking, morphogenesis, immune resp

285 ial-specific genetic manipulations affecting membrane (vesicle) trafficking, the membrane ionic gradi

286 pendent exchange can be uncoupled from outer membrane vesicle/tube formation, reported elsewhere to m

287 spholipases, exoproteases, phenazines, outer membrane vesicles, type III secreted effectors, flagella

288 sly translocate H(+) and Na(+) into inverted membrane vesicles under physiological conditions.

289 mping stoichiometry of complex I in inverted membrane vesicles under steady-state ADP-phosphorylating

290 ed with a control meningococcal native outer membrane vesicle vaccine had similar serum bactericidal

291 to recombinant FHbp vaccines or native outer membrane vesicle vaccines with overexpressed FHbp.

292 that enveloped virions were housed in single-membraned vesicles; viral particles were not observed in

293 ; however, the protein profile of the mutant membrane vesicles was significantly altered, including r

294 endent taurocholate transport in canalicular membrane vesicles, was induced by 90% (P < 0.05).

295 nance experiments and interaction studies in membrane vesicles, we find that in the absence of ATP th

296 s of serine uptake by placental microvillous membrane vesicles were carried out and the model applied

297 to generation of the autophagosome, a double-membrane vesicle, which is targeted to the lysosome.

298 Exosomes are extracellular membrane vesicles whose biogenesis by exocytosis of mult

299 d secretion mediated by exocytotic fusion of membrane vesicles with the plasma membrane is essential

300 stabilized domain separation in Giant Plasma Membrane Vesicles without affecting protein partitioning