ライフサイエンスコーパス: clathrin coat

1 uding those that regulate disassembly of the clathrin coat.

2 o the correct spatiotemporal assembly of the clathrin coat.

3 the cell surface and link them to the PM and clathrin coat.

4 of clathrin-binding adaptor proteins and the clathrin coat.

5 ished for clathrin-AP-1/AP-2 coats, to a non-clathrin coat.

6 organization of the inner AP-1 layer of the clathrin coat.

7 regulation to ensure the correct assembly of clathrin coats.

8 on structural elements with COPI, COPII, and clathrin coats.

9 pe and results in loss of ARH from endocytic clathrin coats.

10 Clathrin coat accessory proteins play key roles in trans

11 omyces cerevisiae, regulates the behavior of clathrin coats after the recruitment of clathrin.

12 h a perturbation of the coupling between the clathrin coat and the actin cytoskeleton, which we confi

13 entral roles in coordinating the assembly of clathrin coats and cargo selection.

14 oated vesicle, or with an in vitro assembled clathrin coat, and recruits Hsc70 to its specific heavy-

15 yotes, and many of the proteins required for clathrin coat assembly and disassembly have orthologs in

16 Clathrin coat assembly on membranes requires cytosolic a

17 functions in clathrin-mediated endocytosis, clathrin coat assembly protein AP180, was quantified as

18 ribosylation factor 1 (ARF1), essential for clathrin coat assembly, Golgi architecture, and vesicula

19 to clathrin-coated pits (CCPs) or initiating clathrin-coat assembly around the cargo molecules.

20 n, triggering clathrin recruitment and hence clathrin-coated bud formation.

21 s was not accompanied by the accumulation of clathrin coated buds on their surface and this process p

22 ular plasma membrane invaginations capped by clathrin-coated buds, occurs selectively at inhibitory s

23 ch in metazoans links endocytic cargo to the clathrin coat, but had no assigned function in yeast, wa

24 for the docking of numerous other important clathrin coat components at the nascent bud site.

25 tection and tracking of fluorescently tagged clathrin coat components within cultured cells.

26 d the genes encoding a set of early arriving clathrin-coat constituents, FCHO1 and FCHO2, in HeLa cel

27 Inducible overexpression of the Arabidopsis clathrin coat disassembly factor, Auxilin2, which inhibi

28 In mammalian systems, clathrin coat disassembly has been reconstituted using n

29 te and facilitates compensatory endocytosis, clathrin-coat disassembly, and vesicle reavailability at

30 Spatiotemporal heterogeneity of clathrin coat dynamics is also observed during morpholog

31 n adaptor whose most critical function(s) in clathrin coat dynamics remain(s) elusive.

32 cant spatiotemporal alterations in endocytic clathrin coat dynamics.

33 e fission, which resulted in accumulation of clathrin-coated endocytic intermediates on the plasma me

34 ce also indicates that Ulk1/2 mediates a non-clathrin-coated endocytosis in sensory growth cones.

35 h Vps class C/HOPS subunits incorporate into clathrin-coated endosomal domains and carriers in mammal

36 e a parallel pathway for AP-2 activation and clathrin-coat fabrication.

37 pical endocytic adaptor critical for optimal clathrin coat formation.

38 -active processes-vacuolar acidification and clathrin-coat formation--as modulators of sertraline's a

39 nistic models for disassembly of nonneuronal clathrin coats has been limited by the absence of a func

40 of the heat shock response or disassembly of clathrin coats, however, where binding of a short hydrop

41 at about 11 A resolution, the structure of a clathrin coat (in the D6-barrel form) with specifically

42 ls of tonic activity leading to a buildup of clathrin-coated intermediates in these synapses.

43 cytic defects and a striking accumulation of clathrin-coated intermediates, strongly implicating Sac

44 ecreased dynamin recruitment to the necks of clathrin-coated invaginations resulting in impaired vesi

45 tor protein 4 (AP-4) is a component of a non-clathrin coat involved in protein sorting at the trans-G

46 chain of botulinum toxin C, nor by block of clathrin-coat maturation.

47 abled researchers to observe the dynamics of clathrin-coated pit (CCP) assembly in real time.

48 or protein 2 (AP2) complexes, which initiate clathrin-coated pit (CCP) assembly, are activated by con

49 Live-cell imaging of individual clathrin-coated pit (CCP) dynamics has revealed a broad

50 Analysis of clathrin-coated pit (CCP) dynamics led us to propose the

51 This corresponded to a decreased rate of clathrin-coated pit (CCP) initiation and increased lifet

52 DEO ABSTRACT: Some endocytic cargoes control clathrin-coated pit (CCP) maturation, but it is not know

53 ecruitment of cargo molecules into a growing clathrin-coated pit (CCP).

54 raphy to investigate the massive increase in clathrin-coated pit abundance that is selectively observ

55 In this paper, we describe a study of clathrin-coated pit dynamics in living cells using ion c

56 , exhibit increased rates of CME and altered clathrin-coated pit dynamics.

57 synthesis and its metabolic processing, the clathrin-coated pit endocytosis pathway, and the ubiquit

58 importance of molecular events required for clathrin-coated pit initiation.

59 activity of neutral sphingomyelinase but not clathrin-coated pit maturation.

60 or proteins facilitate cargo recruitment and clathrin-coated pit nucleation.

61 s, confirming that uptake is mediated by the clathrin-coated pit pathway.

62 When and where a clathrin-coated pit will form and what cargo it will con

63 blocked by a dominant negative mutant of the clathrin-coated pit-associated protein Eps15.

64 after a 4 h chase and became undetectable if clathrin-coated pit-mediated trafficking was blocked wit

65 Classical CME proceeds via the formation of clathrin-coated pits (CCPs) at the plasma membrane, whic

66 Clathrin-coated pits (CCPs) in proximity to substrate co

67 ns (EAPs) mediate assembly and maturation of clathrin-coated pits (CCPs) into cargo-containing vesicl

68 Consistently, Lpd localizes to clathrin-coated pits (CCPs) just before vesicle scission

69 es of the observed heterogeneous dynamics of clathrin-coated pits (CCPs) might be the different cargo

70 rgo receptors, either recruiting cargos into clathrin-coated pits (CCPs) or initiating clathrin-coat

71 ntrol its fate by regulating the dynamics of clathrin-coated pits (CCPs) that mediate their internali

72 ing structures at the plasma membrane termed clathrin-coated pits (CCPs) that mediate vesicle formati

73 substantial increase in the ratio of "open" clathrin-coated pits (CCPs) to "necked"/"closed" CCVs an

74 composition of the lifetime distributions of clathrin-coated pits (CCPs) to measure independent aspec

75 P(2) levels and is concentrated at endocytic clathrin-coated pits (CCPs) via interactions with the sc

76 CME is initiated by the formation of clathrin-coated pits (CCPs), in which adaptors nucleate

77 cargos are known to accumulate into maturing clathrin-coated pits (CCPs), whether and how cargo recru

78 recruitment of adaptors and clathrin to form clathrin-coated pits (CCPs).

79 te the interaction of BMPRs with proteins in clathrin-coated pits (CCPs).

80 eptors is regulated by their endocytosis via clathrin-coated pits (CCPs).

81 which the GAK was disrupted showed a lack of clathrin-coated pits and a complete block in clathrin-me

82 that results in an accumulation of arrested clathrin-coated pits and a greatly reduced synaptic vesi

83 e clathrin-mediated endocytosis with shallow clathrin-coated pits and a strong reduction in the inter

84 quires both clathrin assembly into endocytic clathrin-coated pits and active Cdc42.

85 ls through receptor-mediated endocytosis via clathrin-coated pits and caveolae, that actin filaments

86 tic adaptor, which is highly concentrated at clathrin-coated pits and coordinates acquisition of bila

87 is, a pathway that involves the formation of clathrin-coated pits and fusion to early endosomes.

88 NM23-H1/H2 localized at clathrin-coated pits and interacted with the proline-ric

89 hat ADAM17 is constitutively internalised by clathrin-coated pits and that physiological stimulators

90 per-resolution images of living cells, using clathrin-coated pits and the transferrin cargo as model

91 ies showed FcRY-mediated internalization via clathrin-coated pits and transport involving early and r

92 Clathrin-coated pits are a major entry portal where asse

93 eptor signaling, in cells in which endocytic clathrin-coated pits are frozen at a deeply invaginated

94 Clathrin-coated pits are well defined, but the identity,

95 Despite the identification of clathrin-coated pits at the cell surface over 30 years a

96 catalyzes the scission of deeply invaginated clathrin-coated pits at the plasma membrane, but the mec

97 classical dynamin, which severs the necks of clathrin-coated pits at the plasma membrane.

98 lex and that both BRAG2 and Arf5 localize to clathrin-coated pits at the plasma membrane.

99 Activated receptors are recruited to clathrin-coated pits by beta-arrestins, scaffolding prot

100 ns can be marked as cargo for inclusion into clathrin-coated pits by common internalization signals (

101 ARH recruits ROMK to clathrin-coated pits for constitutive and WNK1-stimuated

102 ntry that is low-pH dependent occurs through clathrin-coated pits in a manner similar to wild-type vi

103 A subpopulation of clathrin-coated pits in cell bodies and dendrites label

104 is generally believed that the formation of clathrin-coated pits in epithelial cells occurs randomly

105 y ligands, MORs are rapidly internalized via clathrin-coated pits in heterologous cells and dissociat

106 athrin-mediated endocytosis, is recruited to clathrin-coated pits in two sequential phases.

107 but they remain defective in the scission of clathrin-coated pits in vivo.

108 tors recruit and polymerize clathrin to form clathrin-coated pits into which cargo is sorted.

109 ocalization of the SNX9.dynamin-2 complex to clathrin-coated pits is blocked by interactions with the

110 d capsids laterally diffused into assembling clathrin-coated pits less than 30 s after attachment.

111 pendent endocytosis through the formation of clathrin-coated pits on the cell membrane.

112 rin receptors are delivered selectively from clathrin-coated pits on the plasma membrane into a speci

113 e ESCRT-0 complex accumulates at a subset of clathrin-coated pits on the surface of human cells.

114 ocal activity, and axonal boutons containing clathrin-coated pits showed a more pronounced decrease i

115 erized, and it remains controversial whether clathrin-coated pits specialize to internalize particula

116 indings reveal a link between progression of clathrin-coated pits to endocytic vesicles and an activa

117 , these findings indicate that BRAG2 acts at clathrin-coated pits to promote integrin internalization

118 D1A, which encodes a protein associated with clathrin-coated pits where cell-surface receptors reside

119 toplasmic domain of E-selectin or disrupting clathrin-coated pits with hypertonic medium blocked inte

120 Ack is concentrated at clathrin-coated pits, and binds clathrin heavy chain via

121 PS15, a protein required for the assembly of clathrin-coated pits, and DN PAK-1, an obligate mediator

122 Triad3A associates with Arc, localizes to clathrin-coated pits, and is associated with endocytic s

123 oenvironments, three-dimensional tracking of clathrin-coated pits, and long-term imaging spanning >10

124 Lp(a) internalization was also dependent on clathrin-coated pits, and Lp(a) was targeted for lysosom

125 ysically interacts with AP-2, is enriched on clathrin-coated pits, and requires clathrin but not RAB-

126 1 and inducing GLUT1 internalization through clathrin-coated pits, as well as indirectly, by reducing

127 tion of clathrin-coated vesicles, but not of clathrin-coated pits, at synapses.

128 onstruct of EPS15, an essential component of clathrin-coated pits, blocked the entry of RRV into RFs.

129 sion by forming a collar around the necks of clathrin-coated pits, but the specific structural intera

130 thrin interactor, is recruited to late-stage clathrin-coated pits, clinical manifestations have been

131 st partially defined by the cytoskeleton and clathrin-coated pits, in which receptors and G proteins

132 )P(3) biosensors, disappearance of endocytic clathrin-coated pits, nearly complete inhibition of KCNQ

133 At clathrin-coated pits, PI(3)P is produced by the INPP4A h

134 n thought to coordinate cargo selection into clathrin-coated pits, results in a significant impairmen

135 Then as the cargoes being enclosed in clathrin-coated pits, they slow down the active rotation

136 endocytosis of ligand-receptor complexes via clathrin-coated pits, trafficking of the internalized li

137 ntrast to INPP5B visits late stage endocytic clathrin-coated pits, was earlier shown to contain anoth

138 ed mechanism for 7TMR internalization is via clathrin-coated pits, where clathrin and adaptor protein

139 ns in a complex with the GTPase dynamin-2 at clathrin-coated pits, where it provokes fission of vesic

140 accumulate at the base of arrested endocytic clathrin-coated pits, where they support the growth of d

141 -coated vesicles and an increase in U-shaped clathrin-coated pits, which may result from sequestratio

142 ntly, ligand-bound EGFR is incorporated into clathrin-coated pits--membrane structures containing cla

143 h syndrome protein (WASP) assembles actin at clathrin-coated pits.

144 s intracellularly into EEA-1+ endosomes from clathrin-coated pits.

145 g that CAT-1-HA-GFP internalization requires clathrin-coated pits.

146 xclusion of bulky extracellular domains from clathrin-coated pits.

147 or-dependent redistribution of arrestin2L to clathrin-coated pits.

148 nner vesicles/tubules and exocytosis through clathrin-coated pits.

149 centration upon Wnt-induced recruitment into clathrin-coated pits.

150 targets the proteins for internalization via clathrin-coated pits.

151 o in mammalian cells, they are excluded from clathrin-coated pits.

152 est detectable endocytic vesicles arise from clathrin-coated pits.

153 n ECs (HUVECs), increasing NP uptake through clathrin-coated pits.

154 at leads to invagination and then fission of clathrin-coated pits.

155 rin-mediated endocytosis and associates with clathrin-coated pits/vesicles at the plasma membrane.

156 A similar massive increase of clathrin-coated profiles (in this case, of clathrin-coat

157 as key membrane determinants for assembly of clathrin coat proteins that drive formation of clathrin-

158 f endocytosis following MC4R localization to clathrin-coated sites and exclusion of the receptor from

159 The earliest stages of clathrin-coated structure (CCS) assembly involve the rec

160 ar organisms on formation and dissolution of clathrin-coated structures (CCSs) have not been directly

161 we found that actin patches associated with clathrin-coated structures (CCSs) in cultured mouse cell

162 To address whether clathrin-coated structures (CCSs) specialize to internal

163 oth the large insert isoform of myosin VI on clathrin-coated structures and the no-insert isoform on

164 Further, the steady-state morphology of clathrin-coated structures appears to be a manifestation

165 (PIPKIs) lynchpin enzymes in the assembly of clathrin-coated structures at the cell surface.

166 l position of the endocytic protein epsin on clathrin-coated structures at the plasma membrane.

167 Dynamics of endocytic clathrin-coated structures can be remarkably divergent a

168 Plasmalemma clathrin-coated structures range from unitary domed asse

169 ficially dimerized construct of myosin VI on clathrin-coated structures suggests that wild type myosi

170 nse core vesicles) and endocytic structures (clathrin-coated structures) and the proteins associated

171 lathrin machinery, localizes to cell surface clathrin-coated structures, and is enriched in placental

172 ed over a dense network of membrane-resident clathrin-coated structures.

173 nto AP-2 or alter AP-2 deposition at surface clathrin-coated structures.

174 teins are found to regulate the formation of clathrin coats under certain conditions, but can also su

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

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

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

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

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

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

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

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

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

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

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

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

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

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

189 Clathrin-coated vesicle formation is responsible for mem

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

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

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

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

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

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

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

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

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

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

200 Clathrin-coated vesicle uncoating requires ATP and is me

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

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

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

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

205 Clathrin coats vesicles in all eukaryotic cells and has

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

229 Clathrin-coated vesicles are vehicles for intracellular

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

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

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

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

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

235 Clathrin-coated vesicles form by rapid assembly of discr

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

251 Clathrin-coated vesicles play an established role in end

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

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

254 2 may stimulate Gap1 incorporation into AP-1/clathrin-coated vesicles to promote Gap1 trafficking fro

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

286 2-microinjected terminals, without affecting clathrin-coated vesicles.

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

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

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

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

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

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

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

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

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

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

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

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

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

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