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 stituting them in vitro using inverted inner membrane vesicles.

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

5 using a protease protection assay in sealed membrane vesicles.

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

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

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

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

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

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

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

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

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

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

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

17 ultiple avenues, including lysis-independent membrane vesicles.

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

19 e in detergent solution and in reconstituted membrane vesicles.

20 1) and by exocytosis of ATP localized within membrane vesicles.

21 preciated source of bioactive, extracellular membrane vesicles.

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

23 small unilamellar vesicles and giant plasma membrane vesicles.

24 d in their native environment of cytoplasmic membrane vesicles.

25 man rhomboid protease RHBDL2 in giant plasma membrane vesicles.

26 ayed reduced rear release and deposited more membrane vesicles.

27 of efflux was also studied in right-side-out membrane vesicles.

28 ferent bacteria, and are secreted into outer membrane vesicles.

29 nner consistent with the production of outer membrane vesicles.

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

31 Exosomes, submicron membrane vesicles (30-200 nm) secreted by almost all cel

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

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

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

35 4 was present in HSC exosomes, which were bi-membrane vesicles, 50-150 nm in diameter, negatively cha

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

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

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

39 (2+) signals and actively traffic GFP-tagged membrane vesicles along their length.

40 mulatory versus prostimulatory CPSs on outer membrane vesicles also regulated immune responses.

41 Msp in intact organisms or outer membrane vesicles also restricts PIP signaling.

42 ytoplasmic cargo and closes to form a double-membrane vesicle (an autophagosome).

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

44 plex that spans both membranes of the double-membrane vesicle and would allow export of RNA to the cy

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

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

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

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

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

53 ATG2A can extract lipids from membrane vesicles and unload them to other vesicles.

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

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

56 including enveloped viruses, bacterial outer membrane vesicles, and mammalian extracellular vesicles.

57 ia either tunneling nanotubes (TNTs) or shed membrane vesicles, and this changes the phenotype of rec

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

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

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

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

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

63 interacts with and controls localization of membrane vesicle-associated PI3Kalpha to microtubules.

64 ruitment of the MLKL-containing necrosome to membrane vesicle-associated sites of aggregation.

65 and Atg8-play in the formation of the double-membrane vesicle autophagosome, which is the functional

66 lar organelles and proteins, in which double-membraned vesicles (autophagosomes) sequester cytoplasmi

67 hore complexes), sequestosomes within double-membraned vesicles (autophagosomes), and sequestosomes w

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

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

70 fic binding sites on the midgut brush border membrane vesicles (BBMV) of both insect species.

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

72 The trafficking of membrane vesicles between different intracellular organe

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

74 ortantly, intact T. forsythia cells or outer membrane vesicles, both of which carry surface-associate

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

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

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

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

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

80 n pathway in which the formation of a double-membrane vesicle called the autophagosome is a key event

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

82 is a major degradation pathway where double-membrane vesicles called autophagosomes deliver cytoplas

83 cytoplasmic material to lysosomes via double-membrane vesicles called autophagosomes.

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

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

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

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

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

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

90 ght microscopy, which correlates with double-membrane vesicles containing vacuoles observed with elec

91 s, hybrids from dendrimersomes and bacterial membrane vesicles containing YadA, a bacterial adhesin p

92 rial enlargement and the formation of double-membraned vesicles containing cytosolic protein within m

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

94 e establish a vaccination strategy utilizing membrane vesicles derived from epithelial cells to gener

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

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

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

98 Although double-membrane vesicles (DMVs) appear to be a pan-CoV RO eleme

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

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

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

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

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

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

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

106 on of ARF1*GTP molecules required for coated membrane vesicle formation.

107 ream viral protein palmitoylation and double-membrane vesicles formation, that are indispensable for

108 Everted membrane vesicles from cells expressing arsJ accumulated

109 (~80%) was S-acylated in ileal brush border membrane vesicles from human organ donors, as well as in

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

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

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

113 cles from giant dendrimersomes and bacterial membrane vesicles generated from the very stable bacteri

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

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

116 Giant plasma membrane vesicles (GPMVs) are a widely used experimental

117 guishes better lipid domains in giant plasma membrane vesicles (GPMVs) than Laurdan.

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

119 Here, giant plasma membrane vesicles (GPMVs) were employed to quantitativel

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

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

122 e adapted chemical induction of giant plasma membrane vesicles (GPMVs), which require both TMEM16F-de

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

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

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

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

127 Bacterial membrane vesicles have been implicated in a broad range

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

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

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

131 Inverted membrane vesicles (IMVs) prepared from CO-grown cells al

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

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

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

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

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

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

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

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

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

141 Gram-negative bacteria release outer membrane vesicles into the external milieu to deliver ef

142 Bacteria release membrane vesicles into the extracellular environment but

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

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

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

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

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

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

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

150 of FXa by the ZPI-PZ complex on procoagulant membrane vesicles (k(a) ((app)) ~10(7) m(-1) s(-1)) was

151 brane distortion and the production of outer membrane vesicle-like features, while NPs bearing short

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

153 Previously unidentified membrane vesicles lying immediately beneath the plasma m

154 ralise magnetite nanoparticles (MNPs) within membrane vesicles (magnetosomes), which are embedded wit

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

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

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

158 Recently, extracellular membrane vesicle (MV) production has been proposed as a

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

160 Here we characterize and compare the membrane vesicles (MVs) from three different Lactobacill

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

162 Extracellular membrane vesicles (MVs) secreted from symbiont commensal

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

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

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

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

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

168 r stable oligomers of RHBDL2 in giant plasma membrane vesicles of human cells even at concentrations

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

170 Membrane vesicles of this kind, termed exosomes and ecto

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

172 Recently, the outer membrane vesicle (OMV) meningococcal B vaccine, MeNZB, w

173 ic susceptibility, osmotic stress, and outer membrane vesicle (OMV) production, suggesting that these

174 Meningococcal outer membrane vesicle (OMV) vaccines are prepared with deterg

175 Outer membrane vesicle (OMV)- based vaccines have been used to

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

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

178 hibits also impairment in formation of outer-membrane vesicles (OMVs) and pili, as well as several ot

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

180 Outer membrane vesicles (OMVs) are nanoscale proteoliposomes t

181 Outer membrane vesicles (OMVs) are spherical liposomes that ar

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

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

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

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

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

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

188 Outer membrane vesicles (OMVs) isolated from Salmonella Typhim

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

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

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

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

193 The outer membrane vesicles (OMVs) produced by P. gingivalis have

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

195 Bacterial outer membrane vesicles (OMVs) represent an interesting vaccin

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

197 acteria have been described to release outer membrane vesicles (OMVs) that are capable of mediating s

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

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

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

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

202 Gram-negative bacteria produce outer-membrane vesicles (OMVs) that package genetic elements,

203 We further defined that the outer membrane vesicles (OMVs) that were derived from the iden

204 nts, wild-type or attenuated endotoxin outer membrane vesicles (OMVs), or lipopolysaccharide (LPS).

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

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

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

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

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

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

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

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

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

214 ayed increased biogenesis of bacterial outer membrane vesicles (OMVs).

215 amically and selectively packaged into outer membrane vesicles (OMVs).

216 ich the periplasm extrudes into a mega outer membrane vesicle or "MOMV" encased by OM which dynamical

217 D-mediated cross-linking of TatB and TatC in membrane vesicles or, alternatively, creating covalently

218 e this problem, we have adapted giant plasma membrane vesicles (or blebs) from native cell membranes

219 Using quantitative imaging of membrane vesicles, our results demonstrate that long dis

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

221 from infected cells were found within double-membrane vesicles partially composed from the donor cell

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

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

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

225 probiotics, the engineering of Lactobacillus membrane vesicles presents a new avenue for the developm

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

227 Outer membrane vesicles produced by Gram-negative bacteria hav

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

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

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

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

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

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

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

235 Exosomes are nanosized membrane vesicles released from cells after fusion of mu

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

237 For many years, double-layer phospholipid membrane vesicles, released by most cells, were not cons

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

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

240 The formation of membrane vesicles requires the activation of the ADP-rib

241 Extracellular vesicles (EVs) are membrane vesicles secreted by cells and can modulate bio

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 ndreae largely provisions its host via outer-membrane vesicle secretion.

246 somes), sequestosomes flanked by flat double-membraned vesicles (sequestosome:phagophore complexes),

247 ELVs are 100 nm diameter membrane vesicles shed into the urine by the cells linin

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

249 cluding in Aedes aegypti larval brush border membrane vesicles, small unilamellar vesicle liposomes,

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

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

252 Vacuoles contained double-membrane vesicles suggestive of partially assembled viru

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

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

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

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

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

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

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

260 MPs are small membrane vesicles that are highly procoagulant.

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

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

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

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

265 al, as it drives the formation of the double-membrane vesicles that engulf cytosolic material.

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

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

268 ure of specific cytosolic contents in double-membrane vesicles that subsequently fuse with the vacuol

269 beneath the alveoli, a network of flattened membrane vesicles that subtends the plasmalemma.

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

271 was mediated by a fraction of extracellular membrane vesicles that were released by the transduced c

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 assays with rhodamine 6G in purified plasma membrane vesicles, the initial rates of rhodamine 6G flu

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

292 Bacterial membrane vesicles were discovered over 60 years ago and

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

294 The symbionts load SsrA into outer membrane vesicles, which are transported specifically in

295 sociated with virus-induced cytosolic double-membrane vesicles, which may provide a tailored microenv

296 es proteins engage inwards with the internal membrane vesicle whilst 2-fold symmetric horn-like struc

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

298 Here we report the coassembly of human membrane vesicles with dendrimersomes.

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