ライフサイエンスコーパス: coated vesicle

1 s) or by protein-protein interactions (e.g., coated vesicles).

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

3 peared together upon formation of a clathrin-coated vesicle.

4 ore coated-pit pinching and formation of the coated vesicle.

5 pression inhibited the uncoating of clathrin-coated vesicles.

6 ermore, PC7 was present in isolated clathrin-coated vesicles.

7 (+) channel that is internalized by clathrin-coated vesicles.

8 a morphology distinct from that of clathrin-coated vesicles.

9 c70-dependent clathrin uncoating of clathrin-coated vesicles.

10 he ability to inhibit the formation of CopII coated vesicles.

11 jected terminals, without affecting clathrin-coated vesicles.

12 reduction in the internalization of clathrin-coated vesicles.

13 and HCs encoded by chc1-box formed clathrin-coated vesicles.

14 at proteins that drive formation of clathrin-coated vesicles.

15 early secretory pathway is mediated by COPII-coated vesicles.

16 icle scission and also in uncoating Clathrin-coated vesicles.

17 which triggers the formation of new clathrin-coated vesicles.

18 e range of cargo accommodated by human COPII-coated vesicles.

19 nd beta-arrestin 1 (beta-Arr1) into clathrin-coated vesicles.

20 range of cargo proteins packaged into COPII-coated vesicles.

21 al of a postfusion SNARE complex in clathrin-coated vesicles.

22 which comprises the coat framework of COPII-coated vesicles.

23 80, also regulates the formation of clathrin-coated vesicles.

24 rted from the endoplasmic reticulum by COPII coated vesicles.

25 ning cargoes for incorporation into clathrin-coated vesicles.

26 Grb2/Sos1 complexes associated with clathrin-coated vesicles.

27 pits assemble on a membrane and pinch off as coated vesicles.

28 receptors into distinct cohorts of clathrin-coated vesicles.

29 gh its secretory pathway is dependent on GGA-coated vesicles.

30 localization of unsheathed mum with clathrin-coated vesicles.

31 sorting of an ER membrane protein into COPII-coated vesicles.

32 diators of cargo protein sorting in clathrin-coated vesicles.

33 rom the membrane and sequestered in clathrin-coated vesicles.

34 lization of the LDL receptor within clathrin-coated vesicles.

35 cific membrane compartments and pinch off as coated vesicles.

36 ant component of the LC, interacts with COPI-coated vesicles.

37 nt with this, WIPI49 is enriched in clathrin-coated vesicles.

38 Scap to bind COPII proteins for transport in coated vesicles.

39 ot Galpha(q), internalized with the clathrin-coated vesicles.

40 ct from those of well-characterized clathrin-coated vesicles.

41 teins that promote the formation of clathrin-coated vesicles.

42 membrane vesicles, microsomes, and clathrin-coated vesicles.

43 ocytosis and membrane recycling via clathrin-coated vesicles.

44 tein which is involved in uncoating clathrin-coated vesicles.

45 ransport of proteins in COPII (coat protein)-coated vesicles.

46 h CCPs, and DOR is internalized via clathrin-coated vesicles.

47 sis that it participates in the formation of coated vesicles.

48 uptake occurs in both caveolae- and clathrin-coated vesicles.

49 adaptor in mediating SAC1 transport in COPII-coated vesicles.

50 o proteins and promotes assembly of clathrin-coated vesicles.

51 teins' role in the struggle to make clathrin-coated vesicles.

52 ly, in the fission and uncoating of clathrin-coated vesicles.

53 ing its transport in coat protein complex II-coated vesicles.

54 n events, including the scission of clathrin-coated vesicles.

55 C7 requires endocytosis into acidic clathrin-coated vesicles.

56 membrane to begin the formation of clathrin-coated vesicles.

57 0, thus initiating uncoating of the clathrin-coated vesicles.

58 bind cargo and grow in size to form clathrin-coated vesicles.

59 ternalization of PC7 is mediated by clathrin-coated vesicles.

60 endocytosis and is associated with clathrin-coated vesicles.

61 key roles in transport mediated by clathrin-coated vesicles.

62 membrane, which invaginate to form clathrin-coated vesicles, a process that is well understood.

63 The endosome is resolved into coated vesicles after 3 s, which in turn become small-di

64 tion of Golgi-derived coat protomer I (COPI)-coated vesicles after activating or inhibiting signaling

65 l receptor (TCR) internalization by clathrin-coated vesicles after encounter with antigen has been im

66 se cells exhibit an accumulation of clathrin-coated vesicles and an increase in U-shaped clathrin-coa

67 TRAPPII is enriched on COPI (Coat Protein I)-coated vesicles and buds, but not Golgi cisternae, and i

68 through the removal of membrane via clathrin-coated vesicles and by callose synthesis.

69 hat is required for localization to clathrin-coated vesicles and contains a putative pleckstrin-homol

70 ficient mice display an increase in clathrin-coated vesicles and delayed reentry of recycling vesicle

71 ion, including accumulation of free clathrin-coated vesicles and delayed vesicle reavailability, impl

72 protein preparations extracted from clathrin-coated vesicles and directly binds to both clathrin and

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

74 HHV-8 was detected in coated vesicles and in large, smooth-surfaced endocytic

75 at REEP6 is detected in a subset of Clathrin-coated vesicles and interacts with the t-SNARE, Syntaxin

76 ins, we showed that HCVpp enter via clathrin-coated vesicles and require delivery to early but not to

77 related JC virus can enter cells in clathrin-coated vesicles and subsequently traffic to caveolae, th

78 promoting its internalization into clathrin-coated vesicles and the consequent disassembly of interc

79 lattice organization of individual clathrin-coated vesicles and the disposition of the captured vesi

80 We provide evidence that COPII-coated vesicles and the ER-Golgi fusion machinery are ne

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

82 Moreover, similarities between structures in coated vesicles and those in the NPC support our prior h

83 -ER transport vesicles, different from COPII-coated vesicles and those involved in traffic of VSVG.

84 ound to be associated with isolated clathrin-coated vesicles and to colocalize with clathrin light ch

85 previously found to be enriched in clathrin-coated vesicles and to promote clathrin assembly in vitr

86 r c-Met is rapidly internalized via clathrin-coated vesicles and traffics through an early endosomal

87 pter complex of the "inner" coat in clathrin-coated vesicles, and a heterotrimeric B-subcomplex, whic

88 s from mammalian macrophages, also uses WASH-coated vesicles, and cells expressing dominant negative

89 ts including the nuclear pore complex, COPII-coated vesicles, and inside the nucleus as a transcripti

90 ivity initially produced less glycogen loss, coated vesicles, and microtubule disassembly.

91 1 that are larger than conventional clathrin-coated vesicles, and that undergo long-range translocati

92 structures, including mitochondria, clathrin-coated vesicles, and the actin cytoskeleton, in either H

93 o ribosomal assembly, the formation of Golgi-coated vesicles, and the maintenance of PS asymmetry.

94 rmine the functional specificity of clathrin-coated vesicles, and together they control a multitude o

95 extends to less well characterized types of coated vesicles, and we identify and characterize the fi

96 ulted in the binding of mu1A of the clathrin-coated vesicle AP-1 complex.

97 mately 300-nm diameter) and typical clathrin-coated vesicles ( approximately 90 nm) makes it unlikely

98 evidence that, as in animal cells, clathrin-coated vesicles are a major means of internalisation by

99 ER-derived COPII-coated vesicles are conventionally targeted to the Golgi

100 COPII-coated vesicles are delivered to the early Golgi via dis

101 Clathrin-coated vesicles are important vehicles of membrane traff

102 Coated vesicles are key components of the machinery of v

103 Clathrin-coated vesicles are known to play diverse and pivotal ro

104 Endocytic clathrin-coated vesicles are short-lived transport intermediates

105 Clathrin/AP2-coated vesicles are the principal endocytic carriers ori

106 Clathrin-coated vesicles are vehicles for intracellular trafficki

107 Clathrin-coated vesicle assembly and disassembly is regulated by

108 l PtdIns(4,5)P(2) generation during clathrin-coated vesicle assembly at the synapse.

109 recise sequence of events promoting clathrin-coated vesicle assembly is still debated.

110 We have identified CVAK104 (a coated vesicle-associated kinase of 104 kDa) using a mas

111 Here we show that the coated vesicle-associated kinase SCYL2/CVAK104 plays a c

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

113 tors required both for formation of clathrin-coated vesicles at the TGN (the Chc1p clathrin heavy cha

114 participates in cargo sorting into clathrin-coated vesicles at the trans-Golgi network (TGN) and end

115 rotein involved in the formation of clathrin-coated vesicles at the trans-Golgi network.

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

117 rking Kir2.1 for incorporation into clathrin-coated vesicles at the trans-Golgi.

118 putative identities and included a clathrin-coated vesicle ATPase, peroxisomal farnesylated protein,

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

120 ion, and that epsin is required for clathrin-coated vesicle budding in cells.

121 tion that measures coat subunit assembly and coated vesicle budding on chemically defined synthetic l

122 ing Drs2p and how it contributes to clathrin-coated vesicle budding remain unclear.

123 in for unsaturated lipids, and are sites for coated vesicle budding.

124 er auxilin or GAK, not only uncoats clathrin-coated vesicles but also acts as a chaperone during clat

125 l of receptors from the membrane in clathrin-coated vesicles, but it remains unclear how clathrin rec

126 TPase dynamin promotes formation of clathrin-coated vesicles, but its mode of action is unresolved.

127 lins results in the accumulation of clathrin-coated vesicles, but not of clathrin-coated pits, at syn

128 COPI coated vesicles carry material between Golgi compartment

129 Clathrin-coated vesicles carry traffic from the plasma membrane t

130 equential region required to uncoat clathrin-coated vesicles catalytically.

131 incorporation into AP-1-containing clathrin-coated vesicles, caused loss of TGN localization and som

132 ) were required for plasma membrane clathrin-coated vesicle (CCV) budding and marked sites of CCV for

133 EpsinR is a clathrin-coated vesicle (CCV) enriched 70-kD protein that binds t

134 species, actin assembly facilitates clathrin-coated vesicle (CCV) formation during endocytosis.

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

136 We then tested whether the clathrin-coated vesicle (CCV)-associated proteins could be phosph

137 cargo to visualize the formation of clathrin-coated vesicles (CCVs) at single CCPs with a time resolu

138 Clathrin-coated vesicles (CCVs) facilitate the transport of cargo

139 te proteomics approach to analyzing clathrin-coated vesicles (CCVs) from HeLa cells.

140 en proposed to involve formation of clathrin-coated vesicles (CCVs) from immature SGs (ISGs).

141 subcellular fractions enriched for clathrin-coated vesicles (CCVs) indicated that pip5k1 and pip5k2

142 The size of endocytic clathrin-coated vesicles (CCVs) is remarkably uniform, suggesting

143 n particular, it is unknown whether clathrin-coated vesicles (CCVs) participate in this transport ste

144 f J-domain proteins load Hsp70 onto clathrin-coated vesicles (CCVs) to drive uncoating.

145 ng signals for packaging cargo into clathrin-coated vesicles (CCVs), and also facilitate down-regulat

146 ein-2 (AP2), a central component of clathrin-coated vesicles (CCVs), is pivotal in clathrin-mediated

147 entire population of intracellular clathrin-coated vesicles (CCVs), suggesting a more global functio

148 e adaptor protein (AP) complexes of clathrin-coated vesicles (CCVs), together with an FKBP and rapamy

149 eads to presynaptic accumulation of clathrin-coated vesicles (CCVs)-all without decreasing GABAergic

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

151 uration before pinching off to form clathrin-coated vesicles (CCVs).

152 ion of AP2 uncoating from endocytic clathrin-coated vesicles (CCVs).

153 nvestigate mechanical properties of clathrin-coated vesicles (CCVs).

154 During the formation of clathrin-coated vesicles, clathrin and endocytic accessory protei

155 Coated vesicles concentrate and package cargo molecules

156 Endoplasmic Reticulum (ER)-derived COPII coated vesicles constitutively transport secretory cargo

157 endosome sorting process begins at clathrin-coated vesicles, depends on microtubule-dependent motili

158 or proteins, leading to cargo packaging into coated vesicles destined for the endolysosomal system.

159 erone for Hsc70 in the uncoating of clathrin-coated vesicles during endocytosis.

160 on is to remove missorted proteins by small, coated vesicles during maturation of these spherical org

161 it the formation of clathrin-coated pits and coated vesicles during synaptic vesicle endocytosis.

162 exomer leading to the capture of Fus1p into coated vesicles en route to the cell surface.

163 hrin heavy chain and is involved in clathrin-coated vesicle endocytosis.

164 ation protocols were used to obtain modified coated vesicle-enriched fractions, which were compared b

165 COPII-coated vesicles export newly synthesized proteins from t

166 that the binding of TRAPPI to Sec23 marks a coated vesicle for fusion with another COPII vesicle or

167 t the TGN, resulting in p14 sorting into AP1-coated vesicles for anterograde TGN-plasma membrane tran

168 nd beta'-COP subunits and packaged into COPI-coated vesicles for Golgi-to-ER retrieval.

169 o proteins to incorporate them into clathrin-coated vesicles for trafficking.

170 tic cells packages cargo proteins into COPII-coated vesicles for transport from the endoplasmic retic

171 COPI-coated vesicles form at the Golgi apparatus from two cyt

172 Clathrin-coated vesicles form by rapid assembly of discrete coat

173 Instead, blockade of clathrin-coated vesicle formation and forward trafficking prevent

174 be involved in both the initiation of COPII-coated vesicle formation and scission of the nascent ves

175 rate to increase the probability of clathrin-coated vesicle formation and to control the number, size

176 e 15) is well known for its role in clathrin-coated vesicle formation at the plasma membrane through

177 or protein-1 (AP1), responsible for clathrin-coated vesicle formation at the trans-Golgi, was selecti

178 1 deficiency had no apparent effect on COPII-coated vesicle formation in an in vitro assay.

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

180 Clathrin-coated vesicle formation is responsible for membrane tra

181 at Eps15 plays an important role in clathrin-coated vesicle formation not only at the plasma membrane

182 own to depend on dynamin by rapidly blocking coated vesicle formation within seconds of dynasore addi

183 ruit accessory proteins involved in clathrin-coated vesicle formation, but the spectrum of known adap

184 lathrin adaptors are key factors in clathrin-coated vesicle formation, coupling clathrin to cargo and

185 red for multiple distinct stages of clathrin-coated vesicle formation, including coated pit formation

186 ces of cell-substrate attachment in clathrin-coated vesicle formation.

187 lti-modular proteins that stimulate clathrin-coated vesicle formation.

188 Dynamin is essential for clathrin-dependent coated vesicle formation.

189 with the endocytic machinery during clathrin-coated vesicle formation.

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

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

192 AP-3 cofractionates with clathrin-coated vesicle fractions isolated from PC12 cells even a

193 Budding of COPI-coated vesicles from Golgi membranes requires an Arf fam

194 essential for the retrograde traffic of COPI-coated vesicles from the Golgi to the ER.

195 dynamin is required for budding of clathrin-coated vesicles from the plasma membrane, after which th

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

197 The endocytosed NPs remain in clathrin-coated vesicles from which they mediate intracellular de

198 sistent with the formation and detachment of coated vesicles from within large patches.

199 and therefore independent of canonical COPII-coated vesicle function.

200 The clathrin-coated vesicle fuses with an endosome where the pH is lo

201 Clathrin-coated vesicles had no detectable role in virion traffic

202 s in plants, but the involvement of clathrin-coated vesicles has been unclear; a new study provides s

203 ith the trans-Golgi and cytoplasmic clathrin-coated vesicles, implicating huntingtin in vesicle traff

204 In addition, the presence of clathrin-coated vesicles in cells containing elevated levels of c

205 ,K(+)-ATPase alpha(1)-subunits into clathrin-coated vesicles in cells transfected with the S11A mutan

206 ),K(+)-ATPase alpha(1)-subunit into clathrin-coated vesicles in cells transfected with WT and S18A ra

207 mirror the localization of FAM21 to retromer-coated vesicles in cells.

208 ed by ubiquitination, is present in clathrin-coated vesicles in epithelial cells that natively expres

209 The role of clathrin-coated vesicles in receptor-mediated endocytosis is cons

210 sts the involvement of caveolae and clathrin-coated vesicles in the transcytotic process.

211 disassembly of clathrin coats from clathrin-coated vesicles in vitro.

212 ntact V1V0-ATPase from bovine brain clathrin-coated vesicles indicates that the structure of the isol

213 oration of TGN cargo molecules into clathrin-coated vesicle intermediates.

214 s well as the transport velocity of clathrin-coated vesicles involved in endocytosis.

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

216 laboratory indicates that the lifetime of a coated vesicle is extremely short, and assembly of nasce

217 Assembly of a COPI coated vesicle is initiated by the small GTPase Arf1 tha

218 The formation of coated vesicles is a fundamental step in many intracellu

219 tomer and formation of coat protein I (COPI)-coated vesicles is crucial to homeostasis in the early s

220 The proper formation of clathrin-coated vesicles is dependent on, and highly regulated by

221 mediating endocytic trafficking of clathrin-coated vesicles is well established.

222 n-coated profiles (in this case, of clathrin-coated vesicles) is observed at inhibitory synapses of n

223 chain (CHC), the main component of clathrin-coated vesicles, is well characterized for its role in i

224 sis of heterogeneous populations of clathrin-coated vesicles isolated from cells.

225 dense-core particles, liquid-filled, bilayer-coated vesicles/liposomes, and gas-filled bubbles.

226 ein complex found at the cytoplasmic face of coated vesicles located at the Golgi complex.

227 Sar1, and dynamin are core components of the coated vesicle machinery.

228 ity monitors that govern cargo packaging and coated vesicle maturation and as components of the fissi

229 lia, suggesting that disassembly of clathrin-coated vesicles may proceed through a partially uncoated

230 Also, our findings suggest that clathrin-coated vesicles may regulate Megatrachea turnover at the

231 Clathrin-coated vesicles mediate a variety of endocytosis pathway

232 Clathrin-coated vesicles mediate sorting and intracellular transp

233 COPII-coated vesicles mediate the transport of newly synthesiz

234 COPI coated vesicles mediate trafficking within the Golgi app

235 COPI-coated vesicles mediate trafficking within the Golgi app

236 Clathrin-coated vesicles mediate vesicular traffic in cells.

237 In the final coated vesicle, most appendage binding partners are abse

238 e structures larger than the typical protein-coated vesicles must be involved in transport.

239 verning the sorting of a SNARE into clathrin-coated vesicles, namely the direct recognition of the th

240 tures, and is enriched in placental clathrin-coated vesicles, new possibilities for Ced-6/Gulp operat

241 The formation of clathrin-coated vesicles occurs continuously in non-dividing cell

242 roach, we visualized the NEC in situ forming coated vesicles of defined size.

243 We examined the composition of clathrin-coated vesicles on an internal organelle responsible for

244 at AREs and caused aberrant accumulation of coated vesicles on AREs, suggesting a previously unrecog

245 pose that AP180 directs Vamp7B into clathrin-coated vesicles on contractile vacuoles, creating an eff

246 element-binding proteins (SREBPs) into COPII-coated vesicles on endoplasmic reticulum (ER) membranes

247 es offer a valuable system to study clathrin-coated vesicles on internal organelles within eukaryotic

248 Coat protein complex I (COPI)-coated vesicles, one of three major types of vesicular c

249 mics and does not involve clathrin assembly, coated vesicles or membrane cholesterol.

250 of the hydrolase-MPR complexes into clathrin-coated vesicles or transport carriers (TCs) destined for

251 n, associates with a freshly budded clathrin-coated vesicle, or with an in vitro assembled clathrin c

252 tant components for the cleavage of clathrin-coated vesicles, phagosomes, and mitochondria.

253 Clathrin-coated vesicles play an established role in endocytosis

254 rom HeLa cells and identified known clathrin-coated vesicle proteins with >90% accuracy.

255 a universal method for defining the clathrin-coated vesicle proteome and may be adapted for the analy

256 port the first comprehensive insect clathrin-coated vesicle proteome.

257 Protein-coated vesicles provide a major mechanism for intracellu

258 Coated vesicles provide a major mechanism for the transp

259 ociated with neck fission; 26 are enough for coated vesicle release in cells partially depleted of dy

260 Sorting of transmembrane cargo into clathrin-coated vesicles requires endocytic adaptors, yet RNA int

261 We conclude that, similar to coated vesicles, several copies of the same structural b

262 ) are too big to fit into conventional COPII-coated vesicles, so how are these bulky cargoes exported

263 ncreases the number of postsynaptic clathrin-coated vesicles, some of which traffic NMDA receptors, d

264 m conditions exhibited an increase in axonal coated vesicles, suggesting widespread neurotransmitter

265 we demonstrate the existence of mobile COPII-coated vesicles that completely encapsulate the cargo PC

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

267 lization on the plasma membrane and clathrin-coated vesicles that originated from the plasma membrane

268 COPI proteins oligomerize to form coated vesicles that transport contents between the Golg

269 EC23A is an essential component of the COPII-coated vesicles that transport secretory proteins from t

270 After the internalization of a clathrin-coated vesicle, the vesicle must uncoat to replenish the

271 For clathrin-coated vesicles, the motifs are recognized by clathrin a

272 roteins that influence the lifecycle of COPI-coated vesicles; this conclusion is supported by the obs

273 link ubiquitinated Notch ligands to Clathrin-coated vesicles through other Clathrin adapter proteins.

274 lytically supports the uncoating of clathrin-coated vesicles through recruitment of Hsc70 in an ATP h

275 te the intracellular trafficking of clathrin-coated vesicles through their interaction with several o

276 hat mTRAPPII is a Rab1 GEF that tethers COPI-coated vesicles to early Golgi membranes.

277 ind to the adaptor protein (AP) complexes of coated vesicles to modulate protein traffic, but the mol

278 mulate Gap1 incorporation into AP-1/clathrin-coated vesicles to promote Gap1 trafficking from endosom

279 rafficking of cargo via a subset of Clathrin-coated vesicles to selected membrane sites in retinal ro

280 ily protein driven, such as the formation of coated vesicles, to those that are primarily lipid drive

281 GGA proteins regulate clathrin-coated vesicle trafficking by interacting with multiple

282 ur results reveal the importance of clathrin-coated vesicle trafficking in C. burnetii infection and

283 nclude effector endocytosis through clathrin-coated vesicle trafficking, defense signaling through me

284 Coat protein II (COPII)-coated vesicles transport proteins and lipids from the e

285 Clathrin-coated vesicle uncoating requires ATP and is mediated by

286 hoinositide phosphatase involved in clathrin-coated vesicle uncoating.

287 ed strong inhibition against bovine clathrin-coated vesicle V-ATPase (10 nM).

288 ATPase (V-ATPase) from bovine brain clathrin coated vesicles was analyzed by electron microscopy and

289 In contrast, when budding of clathrin-coated vesicles was blocked at the plasma membrane or tr

290 in that plays major role in the formation of coated vesicles, was slower in rsw4 than in the control.

291 Otherwise, normal docking and clathrin-coated vesicles were observed, albeit at much reduced nu

292 k and plasma membrane, and abundant clathrin coated vesicles were recruited to the region of nascent

293 rmore, mum failed to associate with clathrin-coated vesicles when receptor destabilization was inhibi

294 exit the endoplasmic reticulum (ER) in COPII-coated vesicles, whereas resident and misfolded proteins

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

296 a core component of coat protein complex II-coated vesicles, which transport secretory proteins from

297 y components are returned to the ER via COPI-coated vesicles, which undergo similar tethering and fus

298 ate secretory route are mediated by clathrin-coated vesicles, while the COat Protein I and II (COPI a

299 equired for the fusion of endocytic clathrin-coated vesicles with endosomes and also for subsequent p

300 omplexes) link the outer lattice of clathrin-coated vesicles with membrane-anchored cargo molecules.