ライフサイエンスコーパス: clathrin-coated pit

1 ne 256, and an intact actin cytoskeleton and clathrin coated pit.

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

3 of endothelial cells but is internalized in clathrin-coated pits.

4 is not necessary for its internalization by clathrin-coated pits.

5 or clathrin, the major structural protein of clathrin-coated pits.

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

7 itionally been viewed as being initiated via clathrin-coated pits.

8 ed together with transferrin receptor and to clathrin-coated pits.

9 ted signaling molecules, and the presence of clathrin-coated pits.

10 d to be internalized rapidly, likely through clathrin-coated pits.

11 n levels, and are distinct from caveolae and clathrin-coated pits.

12 ired for ARH-associated LDLR clustering into clathrin-coated pits.

13 ell as association of adaptor protein-2 with clathrin-coated pits.

14 Nef down-regulates CD4 by linking CD4 to clathrin-coated pits.

15 we observe that SNX9 partially localizes to clathrin-coated pits.

16 namin might guide or insert the complex into clathrin-coated pits.

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

18 any proteins, including beta-arrestin-2 with clathrin-coated pits.

19 two processes promote endocytosis of Smo in clathrin-coated pits.

20 , and not in assembly of functionally active clathrin-coated pits.

21 usly that PSMA undergoes internalization via clathrin-coated pits.

22 hat have been implicated in the formation of clathrin-coated pits.

23 ling through spatial segregation of a GAP in clathrin-coated pits.

24 arized cells but are prevented from entering clathrin-coated pits.

25 nitial steps of EGFR internalization through clathrin-coated pits.

26 -mediated phosphorylation directs it through clathrin-coated pits.

27 in, suggesting that endocytosis occurred via clathrin-coated pits.

28 receptor desensitization and endocytosis via clathrin-coated pits.

29 role in mediating arrestin interaction with clathrin-coated pits.

30 ing the recruitment of the receptor/cargo to clathrin-coated pits.

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

32 e channel that undergoes endocytosis through clathrin-coated pits.

33 rtonic medium, suggesting the involvement of clathrin-coated pits.

34 hese kinases in EGFR internalization through clathrin-coated pits.

35 an chemoattractant receptors internalize via clathrin-coated pits.

36 initiates redistribution of occupied uPAR to clathrin-coated pits.

37 ndocytosis of G protein-coupled receptors by clathrin-coated pits.

38 go rapid, agonist-induced internalization by clathrin-coated pits.

39 roofed' cells showed that Hip1R localizes to clathrin-coated pits.

40 ependent pathway for internalization through clathrin-coated pits.

41 es internalization of the sst2A receptor via clathrin-coated pits.

42 teins entering the endocytic pathway through clathrin-coated pits.

43 clathrin binding motif are still targeted to clathrin-coated pits.

44 naptotagmin fragment had a reduced number of clathrin-coated pits.

45 in the cell cytosol and primes it to reform clathrin-coated pits.

46 targeting of beta(2)-adrenergic receptor to clathrin-coated pits.

47 ological role in the nucleation of endocytic clathrin-coated pits.

48 min I-dependent process that likely involves clathrin-coated pits.

49 olocalize with alpha-adaptin, a component of clathrin-coated pits.

50 soproterenol and colocalizes with beta2AR in clathrin-coated pits.

51 itosis due to a block in the invagination of clathrin-coated pits.

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

53 cludes the agonist-occupied receptors to the clathrin-coated pits.

54 n adaptor incorporation into plasma membrane clathrin-coated pits.

55 d occurs independently of internalization by clathrin-coated pits.

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

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

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

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

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

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

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

63 acterized mechanism for endocytosis involves clathrin-coated pits [1], but evidence has accumulated f

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

65 ing or in the ability to target receptors to clathrin-coated pits, acted as dominant negative inhibit

66 apse leads to a block in the invagination of clathrin-coated pits adjacent to the active zone and the

67 s but was not phosphorylated or recruited to clathrin-coated pits after activation.

68 of these long plasmalemmal invaginations had clathrin-coated pits along their cytoplasmic surface.

69 s believed to contribute to the formation of clathrin-coated pits, although the specific components t

70 ARH colocalizes with megalin in clathrin coated pits and in recycling endosomes in the G

71 Clathrin coated pits and numerous uncoated intracellular

72 tiate the endocytosis of these receptors via clathrin coated-pits and interact directly with clathrin

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

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

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

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

77 ells it colocalizes with clathrin and AP2 in clathrin-coated pits and at the leading edge of migratin

78 show that OCRL visits late-stage, endocytic clathrin-coated pits and binds the Rab5 effector APPL1 o

79 es scission from the plasma membrane of both clathrin-coated pits and caveolae during distinct endocy

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

81 pathway that is insensitive to inhibitors of clathrin-coated pits and caveolae.

82 als, these peptides inhibit the formation of clathrin-coated pits and coated vesicles during synaptic

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

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

85 By EM, HIV virions were seen in clathrin-coated pits and in cytoplasmic vacuoles.

86 mplex, which were concentrated at late-stage clathrin-coated pits and in lamellipodia, also dissociat

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

88 demonstrate that E-selectin clusters in both clathrin-coated pits and lipid rafts of endothelial cell

89 as to test whether cortactin associates with clathrin-coated pits and participates in receptor-mediat

90 least two distinct endocytic pathways (i.e., clathrin-coated pits and plasma membrane lipid rafts) th

91 ation by a process involving endocytosis via clathrin-coated pits and subsequent sorting to lysosomes

92 in-coupled receptors for internalization via clathrin-coated pits and that its endocytic function is

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

94 The sorting of specific proteins into clathrin-coated pits and the mechanics of membrane invag

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

96 docytic trafficking; it is recruited to both clathrin-coated pits and to ensuing uncoated endocytic v

97 , a membrane protein that is endocytosed via clathrin-coated pits and traffics through the acidic end

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

99 in 1 related (Hip1R) is a novel component of clathrin-coated pits and vesicles and is a mammalian hom

100 hese data show that mHip1R is a component of clathrin-coated pits and vesicles and suggest that it mi

101 The lattices of clathrin-coated pits and vesicles are comprised of trisk

102 st component Sec5 is unexpectedly present in clathrin-coated pits and vesicles at the plasma membrane

103 amin-1 (K44A), and MUC1 was observed in both clathrin-coated pits and vesicles by immunoelectron micr

104 wed that virus particles concentrated within clathrin-coated pits and vesicles early in the uptake pr

105 the entire cellular machineries, such as the clathrin-coated pits and vesicles.

106 ynaptojanin 2 depletion causes a decrease in clathrin-coated pits and vesicles.

107 rylation events taking place at the level of clathrin-coated pits and vesicles.

108 nduced a selective increase in unconstricted clathrin-coated pits and, in the case of swinholide, an

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

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

111 molecules from the plasma membrane, through clathrin-coated pits, and into the cell for lysosomal de

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

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

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

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

116 h respect to G proteins, internalization via clathrin-coated pits, and signaling via a growing list o

117 AP-2 complex responsible for the assembly of clathrin-coated pits, and that AP50 is essential for fun

118 at BKV entered into HRPTEC via caveolae, not clathrin-coated pits, and that BKV is maximally associat

119 ceptors are most likely internalized through clathrin-coated pits, and then returned to the plasma me

120 t likely to be internalized independently of clathrin-coated pits, and there is evidence to suggest t

121 alized with clathrin and other components of clathrin-coated pits, AP-2 did not seem to be present in

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

123 We conclude that clathrin-coated pits are dynamic structures with rapid e

124 ree clathrin in the cytosol, suggesting that clathrin-coated pits are dynamic structures.

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

126 Since clathrin-coated pits are planar structures, whereas CVs

127 ompartment provides additional evidence that clathrin-coated pits are the predominant pathway for end

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

129 1 and inducing GLUT1 internalization through clathrin-coated pits, as well as indirectly, by reducing

130 Clathrin-coated pits assemble on a membrane and pinch of

131 issive Vero cells is slow, is independent of clathrin-coated-pit assembly, is dependent on an intact

132 Clathrin-coated pits associated with the plasma membrane

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

134 f ARF6 leads to an increase in the number of clathrin-coated pits at the apical plasma membrane.

135 Recent studies suggest that the mobility of clathrin-coated pits at the cell surface are restricted

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

137 Clathrin-coated pits at the cell surface select material

138 zine, a compound that induces misassembly of clathrin-coated pits at the cell surface.

139 well as the clathrin adaptors AP2 and AP1 in clathrin-coated pits at the plasma membrane and trans-Go

140 overy after photobleaching, that clathrin in clathrin-coated pits at the plasma membrane exchanges wi

141 2 proteins with membranes, and the number of clathrin-coated pits at the plasma membrane increased wh

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

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

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

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

146 pha subunit showed defective localization to clathrin-coated pits; at high expression levels, the app

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

148 out significantly affecting the structure of clathrin-coated pits, both clathrin and AP2 at the plasm

149 The mechanism of clathrin-coated pit budding has been investigated intens

150 peptides containing the D4 region inhibited clathrin-coated pit budding in vitro.

151 that undergo agonist-induced endocytosis via clathrin-coated pits but differ significantly in their p

152 idly, beta-arrestin directs the receptors to clathrin-coated pits but does not internalize with them.

153 rpromazine HCl, which blocks endocytosis via clathrin-coated pits, but not by nystatin and cholera to

154 bound clathrin is a fundamental property of clathrin-coated pits, but not clathrin baskets, and may

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

156 he transferrin receptor is incorporated into clathrin-coated pits by associating, via tyrosine-based

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

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

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

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

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

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

163 des are thought to play an important role in clathrin-coated pit (CCP) dynamics.

164 cission marks the isolation of a cargo-laden clathrin-coated pit (CCP) from the cell exterior.

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

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

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

168 ion via an increased association of CD4 with clathrin-coated pits (CCP).

169 pithelium (PTE), where it is concentrated in clathrin-coated pits (CCPs) and vesicles in the brush bo

170 Clathrin-coated pits (CCPs) are generally considered a u

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

187 itions that markedly affect the structure of clathrin-coated pits, clathrin exchange was blocked but

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

189 )P(2) breakdown on the dynamics of endocytic clathrin-coated pit components and of the actin regulato

190 participates initially in the maturation of clathrin-coated pits during early stages of synaptic ves

191 that ankyrin plays a role in the budding of clathrin-coated pits during endocytosis.

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

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

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

195 acromolecules are internalized into cells by clathrin-coated pit endocytosis.

196 f megalin, ARH and megalin are first seen in clathrin coated pits followed by sequential localization

197 on, mediated by endocytosis of receptors via clathrin-coated pits followed by sorting to lysosomes, h

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

199 receptors to desensitize and target them to clathrin-coated pits for endocytosis.

200 taarrestin2 target desensitized receptors to clathrin-coated pits for endocytosis.

201 c and tissue culture-adapted strains utilize clathrin-coated pits for entry.

202 results suggest a role for synaptojanin 2 in clathrin-coated pit formation and imply that lipid hydro

203 athrin-binding domain of AP180, which blocks clathrin-coated pit formation but not clathrin-independe

204 nodansylcadaverine (MDC), which both inhibit clathrin-coated pit formation, resulted in decreased inv

205 could be blocked by conditions that prevent clathrin-coated pit formation, suggesting that heregulin

206 PARs is blocked by biochemical inhibition of clathrin-coated pit function or overexpression of a domi

207 standard receptor-mediated endocytosis from clathrin-coated pits (half-time <10 min).

208 ine motif of Nef and the component(s) of the clathrin-coated pits has not been pinpointed.

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

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

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

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

213 -) mice are overtly normal, but have reduced clathrin-coated pits in kidney proximal tubule cells and

214 lization of cargo sorting and endocytosis by clathrin-coated pits in living cells.

215 involvement of receptor phosphorylation and clathrin-coated pits in this process.

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

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

218 n-dependent internalization, indicating that clathrin-coated pits, in concert with mechanisms depende

219 embrane invaginations accumulated, capped by clathrin-coated pits, in synapses of dynamin 1-knockout

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

221 ith lipid rafts, the actin cytoskeleton, and clathrin-coated pits influences B cell signaling and ant

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

223 embrane cholesterol plays a critical role in clathrin-coated pit internalization.

224 crose, which have been reported to transform clathrin-coated pits into clathrin cages just below the

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

226 Clathrin-coated pits invaginate from specific membrane c

227 During clathrin-mediated endocytosis, clathrin-coated pits invaginate to form clathrin-coated

228 in a structural rearrangement of clathrin as clathrin-coated pits invaginate.

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

230 the mechanisms by which the invagination of clathrin-coated pits is blocked in mitosis and their sti

231 alization of G protein-coupled receptors via clathrin-coated pits is dependent on the adaptor protein

232 receptor-mediated cholesterol uptake through clathrin-coated pits is now well understood, the molecul

233 suggests a mechanism by which nucleation of clathrin-coated pits is stimulated by the loading of car

234 However, surprisingly FRAP studies on clathrin-coated pits labeled with green fluorescent prot

235 Eps15 is found at the growing edges of clathrin-coated pits, leading to the hypothesis that it

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

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

238 ceptor internalization via dynamin-dependent clathrin-coated pit mechanisms.

239 transporter that is a critical component of clathrin-coated pit-mediated endocytosis, as well as in

240 Only when the agonist-induced clathrin-coated pit-mediated receptor internalization wa

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

242 Both immature and mature DCs are capable of clathrin-coated pit-mediated uptake of SIV, supporting t

243 that MoMuLV entry does not occur through the clathrin-coated-pit-mediated endocytic pathway.

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

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

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

247 of PP1, suggesting that entry of c-Kit into clathrin-coated pits occurs independently of Src family

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

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

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

251 ylinositol 3-kinase, and dynamin 2, although clathrin-coated pits or caveolae are not required.

252 No clathrin-coated pits or vesicles could be detected in th

253 oma cells, which mediate endocytosis via the clathrin-coated pit pathway and are almost completely in

254 ernalizes desialylated glycoproteins via the clathrin-coated pit pathway and mediates their delivery

255 receptors that are internalized through the clathrin-coated pit pathway in a beta-arrestin- and dyna

256 ernalized and processed normally through the clathrin-coated pit pathway.

257 was internalized, predominantly through the clathrin-coated pit pathway.

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

259 in have a severe block in endocytosis by the clathrin-coated-pit pathway.

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

261 ctly couple TGF-beta receptors to AP2 and to clathrin-coated pits, providing the first in vivo eviden

262 opinocytosis (or phagocytosis), formation of clathrin-coated pits (receptor mediated), and penetratio

263 many chemokine receptors internalize through clathrin-coated pits, regulation of the receptor traffic

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

265 sis of transmembrane receptors requires that clathrin-coated pits retain the receptors long enough to

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

267 decreased the recruitment of P-selectin into clathrin-coated pits, slowed the internalization of P-se

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

269 e involvement of adaptor proteins present in clathrin-coated pits, such as epsin, Eps15 (epidermal gr

270 with EGF-R, but with CD71, which is found in clathrin-coated pits, suggesting that integration of tre

271 The clathrin-coated pits that internalize cross-linked recep

272 transient burst of EGFP-SNX9 recruitment to clathrin-coated pits that occurs during the late stages

273 y of auxilin is required for constriction of clathrin-coated pits, the same early step in endocytosis

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

275 egulated by dynamin-dependent endocytosis in clathrin-coated pits through its cytoplasmic domain.

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

277 ycling, and hence in oocytes is recruited to clathrin-coated pits to facilitate the rapid recycling o

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

279 m of Eps15 that is an essential component of clathrin-coated pits, to investigate the extent and impo

280 Thus activated PAR1 internalizes via clathrin-coated pits together with receptors that recycl

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

282 ated at the apical domain co-localizing with clathrin- coated pits/vesicles.

283 tor protein to be identified associated with clathrin-coated pits/vesicles and shown to modulate clat

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

285 t myosin VI associates and co-localizes with clathrin-coated pits/vesicles by its C-terminal tail.

286 on BL-3 cells, LKT moves to lipid rafts and clathrin-coated pits via a dynamic process that results

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

288 e for activated PAR1 internalization through clathrin-coated pits we examined the function of a highl

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

290 The sorting nexin, SNX9, localizes to clathrin-coated pits where it interacts with dynamin and

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

292 Activated PAR1 was rapidly recruited to clathrin-coated pits, where it colocalized with transfer

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

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

295 e it is internalized, P-selectin clusters in clathrin-coated pits, which enhances its ability to supp

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

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

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

299 clathrin triskelions to the edges of growing clathrin-coated pits with very little exchange occurring

300 endocytic defect included an accumulation of clathrin-coated pits with wide necks, as previously obse