ライフサイエンスコーパス: clathrin-coated vesicle

1 hate (PIP(2)) to form the outer layer of the clathrin-coated vesicle.

2 ins disappeared together upon formation of a clathrin-coated vesicle.

3 a strong reduction in the internalization of clathrin-coated vesicles.

4 t manner, and HCs encoded by chc1-box formed clathrin-coated vesicles.

5 ns (CLCa and CLCb) are major constituents of clathrin-coated vesicles.

6 ns in vesicle scission and also in uncoating Clathrin-coated vesicles.

7 ng VDCC and beta-arrestin 1 (beta-Arr1) into clathrin-coated vesicles.

8 f retrieval of a postfusion SNARE complex in clathrin-coated vesicles.

9 og of AP180, also regulates the formation of clathrin-coated vesicles.

10 t solute uptake occurs in both caveolae- and clathrin-coated vesicles.

11 if-containing cargoes for incorporation into clathrin-coated vesicles.

12 may sort receptors into distinct cohorts of clathrin-coated vesicles.

13 ed the colocalization of unsheathed mum with clathrin-coated vesicles.

14 cleared from the membrane and sequestered in clathrin-coated vesicles.

15 e internalization of the LDL receptor within clathrin-coated vesicles.

16 consistent with this, WIPI49 is enriched in clathrin-coated vesicles.

17 in, but not Galpha(q), internalized with the clathrin-coated vesicles.

18 be distinct from those of well-characterized clathrin-coated vesicles.

19 ssory proteins that promote the formation of clathrin-coated vesicles.

20 nalicular membrane vesicles, microsomes, and clathrin-coated vesicles.

21 ed in endocytosis and membrane recycling via clathrin-coated vesicles.

22 in, a protein which is involved in uncoating clathrin-coated vesicles.

23 iated with CCPs, and DOR is internalized via clathrin-coated vesicles.

24 s is achieved by preferential inclusion into clathrin-coated vesicles.

25 AP2 adaptor proteins, integral components of clathrin-coated vesicles.

26 athrin coat proteins that drive formation of clathrin-coated vesicles.

27 these "free-floating" TGN cisternae produce clathrin-coated vesicles.

28 P-2) constitute the major coat components of clathrin-coated vesicles.

29 isassembly and curvature during formation of clathrin-coated vesicles.

30 are poorly incorporated into AP-1-containing clathrin-coated vesicles.

31 embrane, which triggers the formation of new clathrin-coated vesicles.

32 ions rather than cooperatively destabilizing clathrin-coated vesicles.

33 ted by the J-domain protein auxilin, uncoats clathrin-coated vesicles.

34 ged by their ability to remove clathrin from clathrin-coated vesicles.

35 s, which are known to recruit receptors into clathrin-coated vesicles.

36 CPY sorting to the vacuole in the absence of clathrin-coated vesicles.

37 s uncovering enzyme was detected in purified clathrin-coated vesicles.

38 f auxilin, which stimulates the uncoating of clathrin-coated vesicles.

39 embly of Grb2/Sos1 complexes associated with clathrin-coated vesicles.

40 AP)-2 and clathrin, and enriched in purified clathrin-coated vesicles.

41 bule NHE3 leading to endocytosis of NHE3 via clathrin-coated vesicles.

42 hat the uncovering enzyme is endocytosed via clathrin-coated vesicles.

43 of clathrin present in fractions enriched in clathrin-coated vesicles.

44 ind clathrin in vitro and cofractionate with clathrin-coated vesicles.

45 motes the assembly and restricts the size of clathrin-coated vesicles.

46 ependent protein transport being mediated by clathrin-coated vesicles.

47 ortant mediators of cargo protein sorting in clathrin-coated vesicles.

48 isms whereby CFTR could enter such endocytic clathrin-coated vesicles.

49 cal microscopy, was partially colocalized to clathrin-coated vesicles.

50 c70 to dissociate clathrin from bovine brain clathrin-coated vesicles.

51 it is still uncertain whether AP-3 nucleates clathrin-coated vesicles.

52 2 to facilitate efficient entry of CFTR into clathrin-coated vesicles.

53 es is marked by the accumulation of yolk via clathrin-coated vesicles.

54 n rat liver, bovine testes, and bovine brain clathrin-coated vesicles.

55 uits cargo proteins and promotes assembly of clathrin-coated vesicles.

56 n the proteins' role in the struggle to make clathrin-coated vesicles.

57 espectively, in the fission and uncoating of clathrin-coated vesicles.

58 ne fission events, including the scission of clathrin-coated vesicles.

59 that eventually pinch off and internalize as clathrin-coated vesicles.

60 TfR1 by PC7 requires endocytosis into acidic clathrin-coated vesicles.

61 he plasma membrane to begin the formation of clathrin-coated vesicles.

62 uits Hsc70, thus initiating uncoating of the clathrin-coated vesicles.

63 s); they bind cargo and grow in size to form clathrin-coated vesicles.

64 w that internalization of PC7 is mediated by clathrin-coated vesicles.

65 stage of endocytosis and is associated with clathrin-coated vesicles.

66 eins play key roles in transport mediated by clathrin-coated vesicles.

67 diated expression inhibited the uncoating of clathrin-coated vesicles.

68 Furthermore, PC7 was present in isolated clathrin-coated vesicles.

69 nephron K(+) channel that is internalized by clathrin-coated vesicles.

70 coat with a morphology distinct from that of clathrin-coated vesicles.

71 rt the Hsc70-dependent clathrin uncoating of clathrin-coated vesicles.

72 2-microinjected terminals, without affecting clathrin-coated vesicles.

73 n pancreatic beta-cells, the budding of AP-1/clathrin-coated vesicles, a portion of which is derived

74 ave been demonstrated to internalize through clathrin-coated vesicles, a process that involves the bi

75 he plasma membrane, which invaginate to form clathrin-coated vesicles, a process that is well underst

76 T cell receptor (TCR) internalization by clathrin-coated vesicles after encounter with antigen ha

77 nals, there was a persistent accumulation of clathrin-coated vesicles and a backup of newly reformed

78 These cells exhibit an accumulation of clathrin-coated vesicles and an increase in U-shaped cla

79 partner of huntingtin, copurifies with brain clathrin-coated vesicles and associates directly with bo

80 t (PFS), through the removal of membrane via clathrin-coated vesicles and by callose synthesis.

81 region that is required for localization to clathrin-coated vesicles and contains a putative pleckst

82 anin 1-deficient mice display an increase in clathrin-coated vesicles and delayed reentry of recyclin

83 tic function, including accumulation of free clathrin-coated vesicles and delayed vesicle reavailabil

84 adaptor protein preparations extracted from clathrin-coated vesicles and directly binds to both clat

85 An increased number of clathrin-coated vesicles and empty cages were present at

86 nsferrin and demonstrated virus particles in clathrin-coated vesicles and endosome-like structures.

87 AuNPs were also abundant inside the cells in clathrin-coated vesicles and endosomes.

88 eads at either end, and that it can assemble clathrin-coated vesicles and F-actin into higher order s

89 strate that REEP6 is detected in a subset of Clathrin-coated vesicles and interacts with the t-SNARE,

90 compartments were then identified, including clathrin-coated vesicles and pits, large uncoated vesicl

91 lar proteins, we showed that HCVpp enter via clathrin-coated vesicles and require delivery to early b

92 closely related JC virus can enter cells in clathrin-coated vesicles and subsequently traffic to cav

93 ody revealed that TBC1D24 is associated with clathrin-coated vesicles and synapses of hippocampal neu

94 , thereby promoting its internalization into clathrin-coated vesicles and the consequent disassembly

95 study the lattice organization of individual clathrin-coated vesicles and the disposition of the capt

96 localizes to the trans-Golgi network (TGN), clathrin-coated vesicles and the plasma membrane.

97 ns were found to be associated with isolated clathrin-coated vesicles and to colocalize with clathrin

98 eins were previously found to be enriched in clathrin-coated vesicles and to promote clathrin assembl

99 uPAR-LRP complexes are endocytosed via clathrin-coated vesicles and traffic together to early e

100 s receptor c-Met is rapidly internalized via clathrin-coated vesicles and traffics through an early e

101 o the adapter complex of the "inner" coat in clathrin-coated vesicles, and a heterotrimeric B-subcomp

102 um, endosomal compartments, Golgi apparatus, clathrin-coated vesicles, and sarcolemmal membranes were

103 protein-1 that are larger than conventional clathrin-coated vesicles, and that undergo long-range tr

104 ological structures, including mitochondria, clathrin-coated vesicles, and the actin cytoskeleton, in

105 ate protein (hsc70), the uncoating ATPase of clathrin-coated vesicles, and the other as its mitochond

106 kely determine the functional specificity of clathrin-coated vesicles, and together they control a mu

107 hages resulted in the binding of mu1A of the clathrin-coated vesicle AP-1 complex.

108 ( approximately 300-nm diameter) and typical clathrin-coated vesicles ( approximately 90 nm) makes it

109 es strong evidence that, as in animal cells, clathrin-coated vesicles are a major means of internalis

110 Clathrin-coated vesicles are important vehicles of membr

111 Clathrin-coated vesicles are known to play diverse and p

112 Endocytic clathrin-coated vesicles are short-lived transport inter

113 Clathrin-coated vesicles are vehicles for intracellular

114 lattices and the transition to highly curved clathrin-coated vesicles - are adaptable and can follow

115 Clathrin-coated vesicle assembly and disassembly is regu

116 r regional PtdIns(4,5)P(2) generation during clathrin-coated vesicle assembly at the synapse.

117 The precise sequence of events promoting clathrin-coated vesicle assembly is still debated.

118 could be a link between cargo molecules and clathrin-coated vesicle assembly.

119 ctin functions in the intermediate stages of clathrin-coated vesicle assembly.

120 ex-2 (AP-2) is required for the formation of clathrin-coated vesicles at the plasma membrane (PM).

121 amin 2 (Dyn 2) associates predominantly with clathrin-coated vesicles at the plasma membrane and the

122 that factors required both for formation of clathrin-coated vesicles at the TGN (the Chc1p clathrin

123 ndependent mannose 6-phosphate receptor into clathrin-coated vesicles at the TGN, partial redistribut

124 amer that participates in cargo sorting into clathrin-coated vesicles at the trans-Golgi network (TGN

125 or coat protein involved in the formation of clathrin-coated vesicles at the trans-Golgi network.

126 aging the mannose 6-phosphate receptors into clathrin-coated vesicles at the trans-Golgi network.

127 hereby marking Kir2.1 for incorporation into clathrin-coated vesicles at the trans-Golgi.

128 assigned putative identities and included a clathrin-coated vesicle ATPase, peroxisomal farnesylated

129 Clathrin-coated vesicles bud from selected cellular memb

130 ently of coat recruitment to facilitate AP-1/clathrin-coated vesicle budding from the TGN.

131 vesiculation, and that epsin is required for clathrin-coated vesicle budding in cells.

132 ys requiring Drs2p and how it contributes to clathrin-coated vesicle budding remain unclear.

133 ion of myosin VI and Hip1R in actin-mediated clathrin-coated vesicle budding.

134 one, either auxilin or GAK, not only uncoats clathrin-coated vesicles but also acts as a chaperone du

135 isassembling clathrin, not only in uncoating clathrin-coated vesicles but perhaps in preventing unpro

136 ed removal of receptors from the membrane in clathrin-coated vesicles, but it remains unclear how cla

137 is, the GTPase dynamin promotes formation of clathrin-coated vesicles, but its mode of action is unre

138 e endophilins results in the accumulation of clathrin-coated vesicles, but not of clathrin-coated pit

139 ain of the vacuolar ATPase from bovine brain clathrin-coated vesicles by electron microscopy at 21 A

140 is a required cofactor for the uncoating of clathrin-coated vesicles by Hsc70 in non-neuronal cells.

141 studied in vitro as a cofactor for uncoating clathrin-coated vesicles by the chaperone Hsc70.

142 Clathrin-coated vesicles carry traffic from the plasma m

143 minimal sequential region required to uncoat clathrin-coated vesicles catalytically.

144 uce ATP7B incorporation into AP-1-containing clathrin-coated vesicles, caused loss of TGN localizatio

145 (FCHo1/2) were required for plasma membrane clathrin-coated vesicle (CCV) budding and marked sites o

146 Within the clathrin-coated vesicle (CCV) cycle, coat assembly drive

147 EpsinR is a clathrin-coated vesicle (CCV) enriched 70-kD protein tha

148 diverse species, actin assembly facilitates clathrin-coated vesicle (CCV) formation during endocytos

149 and then compared the protein composition of clathrin-coated vesicle (CCV) fractions from control and

150 We then tested whether the clathrin-coated vesicle (CCV)-associated proteins could

151 The membrane-anchored pool is found on clathrin-coated vesicles (CCVs) and pits in rat liver an

152 ensitive cargo to visualize the formation of clathrin-coated vesicles (CCVs) at single CCPs with a ti

153 1) sorts and packages membrane proteins into clathrin-coated vesicles (CCVs) at the TGN and endosomes

154 les of Hsc70 and auxilin in the uncoating of clathrin-coated vesicles (CCVs) during neuronal endocyto

155 Clathrin-coated vesicles (CCVs) facilitate the transport

156 g protein ARF has been implicated in budding clathrin-coated vesicles (CCVs) from Golgi and endosomal

157 ultivariate proteomics approach to analyzing clathrin-coated vesicles (CCVs) from HeLa cells.

158 on has been proposed to involve formation of clathrin-coated vesicles (CCVs) from immature SGs (ISGs)

159 ure has been used to investigate the role of clathrin-coated vesicles (CCVs) in the transport of vacu

160 tests on subcellular fractions enriched for clathrin-coated vesicles (CCVs) indicated that pip5k1 an

161 The size of endocytic clathrin-coated vesicles (CCVs) is remarkably uniform, s

162 In particular, it is unknown whether clathrin-coated vesicles (CCVs) participate in this tran

163 Clathrin-coated vesicles (CCVs) that form at the PM and

164 family of J-domain proteins load Hsp70 onto clathrin-coated vesicles (CCVs) to drive uncoating.

165 as sorting signals for packaging cargo into clathrin-coated vesicles (CCVs), and also facilitate dow

166 ptor protein-2 (AP2), a central component of clathrin-coated vesicles (CCVs), is pivotal in clathrin-

167 on of the entire population of intracellular clathrin-coated vesicles (CCVs), suggesting a more globa

168 its of the adaptor protein (AP) complexes of clathrin-coated vesicles (CCVs), together with an FKBP a

169 ty, and leads to presynaptic accumulation of clathrin-coated vesicles (CCVs)-all without decreasing G

170 e regulation of AP2 uncoating from endocytic clathrin-coated vesicles (CCVs).

171 FM), we investigate mechanical properties of clathrin-coated vesicles (CCVs).

172 dynamin, a gene required for the budding of clathrin-coated vesicles (CCVs).

173 ha could be co-purified with a population of clathrin-coated vesicles (CCVs).

174 (CCPs) that invaginate and pinch off to form clathrin-coated vesicles (CCVs).

175 whether it is critical for CFTR uptake into clathrin-coated vesicles (CCVs).

176 rther maturation before pinching off to form clathrin-coated vesicles (CCVs).

177 During the formation of clathrin-coated vesicles, clathrin and endocytic accesso

178 ain of the early sorting endosome but not on clathrin-coated vesicles, consistent with a role in prov

179 his possibility, we show that immunoisolated clathrin-coated vesicles contain invertase.

180 Following NGF treatment, we found that clathrin-coated vesicles contained NGF bound to TrkA tog

181 sis, clathrin-coated pits invaginate to form clathrin-coated vesicles (CVs).

182 pre-early endosome sorting process begins at clathrin-coated vesicles, depends on microtubule-depende

183 a co-chaperone for Hsc70 in the uncoating of clathrin-coated vesicles during endocytosis.

184 s thought to be required for the assembly of clathrin-coated vesicles during endocytosis.

185 with clathrin heavy chain and is involved in clathrin-coated vesicle endocytosis.

186 sembly, suggesting that ACK2 plays a role in clathrin-coated vesicle endocytosis.

187 Clathrin-coated vesicles execute receptor-mediated endoc

188 l of cargo proteins to incorporate them into clathrin-coated vesicles for trafficking.

189 Clathrin-coated vesicles form by rapid assembly of discr

190 These results establish that AP-3-containing clathrin-coated vesicles form in vitro and are consisten

191 adapter proteins involved in early steps of clathrin coated vesicle formation.

192 Instead, blockade of clathrin-coated vesicle formation and forward traffickin

193 P-2 cooperate to increase the probability of clathrin-coated vesicle formation and to control the num

194 ed cells, we have identified which events in clathrin-coated vesicle formation are accelerated by the

195 rate clone 15) is well known for its role in clathrin-coated vesicle formation at the plasma membrane

196 ults indicate that AP-2 is not essential for clathrin-coated vesicle formation at the plasma membrane

197 thrin adaptor EPSIN1 (EPS1) is implicated in clathrin-coated vesicle formation at the trans-Golgi net

198 of adaptor protein-1 (AP1), responsible for clathrin-coated vesicle formation at the trans-Golgi, wa

199 ology domains and NPF motifs are involved in clathrin-coated vesicle formation during synaptic vesicl

200 nctional evidence for a role of actin during clathrin-coated vesicle formation is lacking.

201 Clathrin-coated vesicle formation is responsible for mem

202 dicate that Eps15 plays an important role in clathrin-coated vesicle formation not only at the plasma

203 endocytosis, but its exact role in endocytic clathrin-coated vesicle formation remains to be establis

204 ct to recruit accessory proteins involved in clathrin-coated vesicle formation, but the spectrum of k

205 Clathrin adaptors are key factors in clathrin-coated vesicle formation, coupling clathrin to

206 are required for multiple distinct stages of clathrin-coated vesicle formation, including coated pit

207 R) are multi-modular proteins that stimulate clathrin-coated vesicle formation.

208 ssociate with the endocytic machinery during clathrin-coated vesicle formation.

209 auxilin also acts during the early steps of clathrin-coated vesicle formation.

210 res a tyrosine-based signal that can mediate clathrin-coated vesicle formation.

211 e influences of cell-substrate attachment in clathrin-coated vesicle formation.

212 However, Hsc70 is also involved in uncoating clathrin-coated vesicles formed at the plasma membrane o

213 AP-3 cofractionates with clathrin-coated vesicle fractions isolated from PC12 cel

214 ndocytosis (CME) occurs via the formation of clathrin-coated vesicles from clathrin-coated pits (CCPs

215 ssembly of clathrin coats and the budding of clathrin-coated vesicles from the neuronal plasma membra

216 ge GTPase dynamin is required for budding of clathrin-coated vesicles from the plasma membrane, after

217 of dynamin, a GTPase required for budding of clathrin-coated vesicles from the plasma membrane.

218 The endocytosed NPs remain in clathrin-coated vesicles from which they mediate intrace

219 The clathrin-coated vesicle fuses with an endosome where the

220 Clathrin-coated vesicles had no detectable role in virio

221 ure of the vacuolar ATPase from bovine brain clathrin-coated vesicles has been determined by electron

222 sis occurs in plants, but the involvement of clathrin-coated vesicles has been unclear; a new study p

223 We previously showed that clathrin-coated vesicles have a dynamic phosphoinositide

224 nd clathrin toward the targeting of GPCRs to clathrin-coated vesicles have not been established.

225 or protein that functions in the assembly of clathrin-coated vesicles; however, biochemical evidence

226 largely with the trans-Golgi and cytoplasmic clathrin-coated vesicles, implicating huntingtin in vesi

227 Although many GPCRs internalize into clathrin-coated vesicles in a dynamin-dependent manner,

228 When Hsc70 uncoats clathrin-coated vesicles in an auxilin- and ATP-dependen

229 In addition, the presence of clathrin-coated vesicles in cells containing elevated le

230 of Na(+),K(+)-ATPase alpha(1)-subunits into clathrin-coated vesicles in cells transfected with the S

231 the Na(+),K(+)-ATPase alpha(1)-subunit into clathrin-coated vesicles in cells transfected with WT an

232 s regulated by ubiquitination, is present in clathrin-coated vesicles in epithelial cells that native

233 The role of clathrin-coated vesicles in receptor-mediated endocytosi

234 ile suggests the involvement of caveolae and clathrin-coated vesicles in the transcytotic process.

235 70 in the disassembly of clathrin coats from clathrin-coated vesicles in vitro.

236 of the intact V1V0-ATPase from bovine brain clathrin-coated vesicles indicates that the structure of

237 In addition, we observed an increase in clathrin-coated vesicles, indicating that the peptide do

238 ve incorporation of TGN cargo molecules into clathrin-coated vesicle intermediates.

239 lecules as well as the transport velocity of clathrin-coated vesicles involved in endocytosis.

240 We found that when the budding of clathrin-coated vesicle is blocked without significantly

241 The proper formation of clathrin-coated vesicles is dependent on, and highly reg

242 aptor, in mediating endocytic trafficking of clathrin-coated vesicles is well established.

243 f clathrin-coated profiles (in this case, of clathrin-coated vesicles) is observed at inhibitory syna

244 rin heavy chain (CHC), the main component of clathrin-coated vesicles, is well characterized for its

245 unctionally active CFTR is found in purified clathrin-coated vesicles isolated from both cultured epi

246 led analysis of heterogeneous populations of clathrin-coated vesicles isolated from cells.

247 Clathrin-coated vesicles lose their clathrin lattice wit

248 al triskelia, suggesting that disassembly of clathrin-coated vesicles may proceed through a partially

249 Also, our findings suggest that clathrin-coated vesicles may regulate Megatrachea turnov

250 Clathrin-coated vesicles mediate a variety of endocytosi

251 Clathrin-coated vesicles mediate sorting and intracellul

252 Clathrin-coated vesicles mediate the transport of the so

253 Clathrin-coated vesicles mediate vesicular traffic in ce

254 etails governing the sorting of a SNARE into clathrin-coated vesicles, namely the direct recognition

255 ted structures, and is enriched in placental clathrin-coated vesicles, new possibilities for Ced-6/Gu

256 The formation of clathrin-coated vesicles occurs continuously in non-divi

257 ed with the trans-Golgi where the budding of clathrin-coated vesicles occurs.

258 We examined the composition of clathrin-coated vesicles on an internal organelle respon

259 We propose that AP180 directs Vamp7B into clathrin-coated vesicles on contractile vacuoles, creati

260 le vacuoles offer a valuable system to study clathrin-coated vesicles on internal organelles within e

261 capture of the hydrolase-MPR complexes into clathrin-coated vesicles or transport carriers (TCs) des

262 e, auxilin, associates with a freshly budded clathrin-coated vesicle, or with an in vitro assembled c

263 aptor complex is involved in the assembly of clathrin-coated vesicles originating from the trans-Golg

264 are important components for the cleavage of clathrin-coated vesicles, phagosomes, and mitochondria.

265 Clathrin-coated vesicles play an established role in end

266 roteins from HeLa cells and identified known clathrin-coated vesicle proteins with >90% accuracy.

267 iling is a universal method for defining the clathrin-coated vesicle proteome and may be adapted for

268 and we report the first comprehensive insect clathrin-coated vesicle proteome.

269 Sorting of transmembrane cargo into clathrin-coated vesicles requires endocytic adaptors, ye

270 ins that participate in the process by which clathrin-coated vesicles retrieve synaptic membranes or

271 ockdown increases the number of postsynaptic clathrin-coated vesicles, some of which traffic NMDA rec

272 CHC17 forms the ubiquitous clathrin-coated vesicles that mediate membrane traffic.

273 n to localization on the plasma membrane and clathrin-coated vesicles that originated from the plasma

274 This transformation involves clathrin-coated vesicles that reduce the relative membra

275 After the internalization of a clathrin-coated vesicle, the vesicle must uncoat to repl

276 For clathrin-coated vesicles, the motifs are recognized by c

277 ls is to link ubiquitinated Notch ligands to Clathrin-coated vesicles through other Clathrin adapter

278 that catalytically supports the uncoating of clathrin-coated vesicles through recruitment of Hsc70 in

279 coordinate the intracellular trafficking of clathrin-coated vesicles through their interaction with

280 2 may stimulate Gap1 incorporation into AP-1/clathrin-coated vesicles to promote Gap1 trafficking fro

281 EEP6 in trafficking of cargo via a subset of Clathrin-coated vesicles to selected membrane sites in r

282 GGA proteins regulate clathrin-coated vesicle trafficking by interacting with

283 Thus, our results reveal the importance of clathrin-coated vesicle trafficking in C. burnetii infec

284 ovides novel insight into the TGN-associated clathrin-coated vesicle trafficking machinery that impac

285 athways include effector endocytosis through clathrin-coated vesicle trafficking, defense signaling t

286 In eukaryotic cells, clathrin-coated vesicles transport specific cargo from t

287 Clathrin-coated vesicle uncoating requires ATP and is me

288 , a phosphoinositide phosphatase involved in clathrin-coated vesicle uncoating.

289 ue 2 showed strong inhibition against bovine clathrin-coated vesicle V-ATPase (10 nM).

290 vacuolar ATPase (V-ATPase) from bovine brain clathrin coated vesicles was analyzed by electron micros

291 In contrast, when budding of clathrin-coated vesicles was blocked at the plasma membr

292 gi network and plasma membrane, and abundant clathrin coated vesicles were recruited to the region of

293 Otherwise, normal docking and clathrin-coated vesicles were observed, albeit at much r

294 Furthermore, mum failed to associate with clathrin-coated vesicles when receptor destabilization w

295 aled that MT1-MMP is internalized rapidly in clathrin-coated vesicles whereas MT1 Delta C remains on

296 Vps class C/HOPS proteins cofractionate with clathrin-coated vesicles, which are devoid of Hrs.

297 More importantly, liver clathrin-coated vesicles, which contain GAK but not auxi

298 and the late secretory route are mediated by clathrin-coated vesicles, while the COat Protein I and I

299 SNAREs, required for the fusion of endocytic clathrin-coated vesicles with endosomes and also for sub

300 ins (AP complexes) link the outer lattice of clathrin-coated vesicles with membrane-anchored cargo mo