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 play central roles orchestrating assembly of 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 n, triggering clathrin recruitment and hence clathrin-coated bud formation.

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

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

22 tein 1 (ACAP1) functions as an adaptor for a clathrin coat complex that has a function in endocytic r

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

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

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

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

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

28 Clathrin coats drive transport vesicle formation from th

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

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

31 cant spatiotemporal alterations in endocytic clathrin coat dynamics.

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

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

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

35 l-free reconstitution system, we report that clathrin coat formation and cargo sorting can be uncoupl

36 pical endocytic adaptor critical for optimal clathrin coat formation.

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

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

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

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

41 Besides AP-2 and clathrin triskelia, clathrin coat inception depends on a group of early-arri

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 cteristic helical structures around necks of clathrin-coated membrane buds.

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

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

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

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

52 ighly sensitive and quantitative analysis of clathrin-coated pit (CCP) dynamics, we have evaluated th

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

54 hat this phosphorylation event starts during clathrin-coated pit (CCP) initiation and increases throu

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

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

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

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

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

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

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

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

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

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

65 r size increases beyond the size of a single clathrin-coated pit, B cells retrieve receptor clusters

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

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

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

69 ations affect the morphology and kinetics of clathrin-coated pits (CCPs) by directly following their

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

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

72 guishing abortive coats (ACs) from bona fide clathrin-coated pits (CCPs) is required but unaccomplish

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

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

75 ed by stabilization and growth/maturation of clathrin-coated pits (CCPs) that eventually pinch off an

76 iated endocytosis occurs via the assembly of clathrin-coated pits (CCPs) that invaginate and pinch of

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

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

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

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

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

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

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

84 e formation of clathrin-coated vesicles from clathrin-coated pits (CCPs).

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

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

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

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

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

90 d bilayer, accompanied by an accumulation of clathrin-coated pits and caveolae.

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

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

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

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

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

96 ns unclear whether the cargos in the growing clathrin-coated pits are actively monitored by the coat

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

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

99 ation of EETI-II-positive macropinosomes and clathrin-coated pits at early time points after treatmen

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

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

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

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

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

105 Without MYO7B or actin filaments, many clathrin-coated pits fail to be severed from the membran

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

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

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

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

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

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

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

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

114 inositol 3-kinase C2alpha at plasma membrane clathrin-coated pits is spatially segregated from its hy

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

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

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

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

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

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

121 tosis depends on the formation of functional clathrin-coated pits that recruit cargos and mediate the

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

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

124 Superresolution imaging of microtubules and clathrin-coated pits was demonstrated, under both modes.

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

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

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

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

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

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

131 s, focal adhesions, primary cilia, caveolae, clathrin-coated pits, and plaques play additional key ro

132 1 and inducing GLUT1 internalization through clathrin-coated pits, as well as indirectly, by reducing

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

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

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

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

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

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

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

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

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

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

143 molecules via endocytic components, such as clathrin-coated pits, vacuoles, and micropinocytic vesic

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

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

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

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

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

149 endocytosis and is undetectable in endocytic clathrin-coated pits.

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

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

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

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

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

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

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

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

158 these proteins are essential for fission of clathrin-coated pits.

159 place throughout the lifetime of the growing clathrin-coated pits.

160 m of the clathrin adaptor protein 2 (AP2) at clathrin-coated pits.

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

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

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

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

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

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

167 the nanoscale structural dynamics of single clathrin-coated sites.

168 This combined approach has strong effects on clathrin coat structure and function by dictating the st

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

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

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

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

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

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

175 Yet, in living cells, EH domains gathered at clathrin-coated structures are poorly accessible, indica

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

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

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

179 Recruitment of receptors into clathrin-coated structures is essential to signal transd

180 Plasmalemma clathrin-coated structures range from unitary domed asse

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

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

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

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

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

186 ration of the weakly recruited receptor into clathrin-coated structures.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

201 Clathrin-coated vesicle formation is responsible for mem

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

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

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

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

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

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

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

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

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

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

212 Clathrin-coated vesicle uncoating requires ATP and is me

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

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

215 Clathrin coats vesicles in all eukaryotic cells and has

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

243 Clathrin-coated vesicles form by rapid assembly of discr

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

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

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

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

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

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

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

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

252 Clathrin-coated vesicles lose their clathrin lattice wit

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

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

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

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

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

258 Clathrin-coated vesicles play an established role in end

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

260 2 may stimulate Gap1 incorporation into AP-1/clathrin-coated vesicles to promote Gap1 trafficking fro

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

291 2-microinjected terminals, without affecting clathrin-coated vesicles.

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

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

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

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

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

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

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

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

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