ライフサイエンスコーパス: coated pit

1 s primarily or exclusively in a newly formed coated pit.

2 cond, with fission of the membrane neck of a coated pit.

3 of bulky extracellular domains from clathrin-coated pits.

4 ons reduce recruitment efficiency of OCRL to coated pits.

5 ent redistribution of arrestin2L to clathrin-coated pits.

6 n upon Wnt-induced recruitment into clathrin-coated pits.

7 imilar to how clathrin attracts molecules to coated pits.

8 cles/tubules and exocytosis through clathrin-coated pits.

9 he proteins for internalization via clathrin-coated pits.

10 n, which binds to the endocytic machinery of coated pits.

11 helial cells but is internalized in clathrin-coated pits.

12 ecessary for its internalization by clathrin-coated pits.

13 in, the major structural protein of clathrin-coated pits.

14 been viewed as being initiated via clathrin-coated pits.

15 er with transferrin receptor and to clathrin-coated pits.

16 ling molecules, and the presence of clathrin-coated pits.

17 nternalized rapidly, likely through clathrin-coated pits.

18 and are distinct from caveolae and clathrin-coated pits.

19 ARH-associated LDLR clustering into clathrin-coated pits.

20 sociation of adaptor protein-2 with clathrin-coated pits.

21 alian cells, they are excluded from clathrin-coated pits.

22 own-regulates CD4 by linking CD4 to clathrin-coated pits.

23 ve that SNX9 partially localizes to clathrin-coated pits.

24 ht guide or insert the complex into clathrin-coated pits.

25 roximately 27-fold excess of LDLR outside of coated pits.

26 ins, including beta-arrestin-2 with clathrin-coated pits.

27 esses promote endocytosis of Smo in clathrin-coated pits.

28 in assembly of functionally active clathrin-coated pits.

29 PSMA undergoes internalization via clathrin-coated pits.

30 been implicated in the formation of clathrin-coated pits.

31 ugh spatial segregation of a GAP in clathrin-coated pits.

32 a clathrin/dephosphin-mediated retrieval via coated pits.

33 lls but are prevented from entering clathrin-coated pits.

34 Grb2 binding sites do not efficiently enter coated pits.

35 eps of EGFR internalization through clathrin-coated pits.

36 phosphorylation directs it through clathrin-coated pits.

37 nter non-raft membrane, from which it enters coated pits.

38 sting that endocytosis occurred via clathrin-coated pits.

39 desensitization and endocytosis via clathrin-coated pits.

40 mediating arrestin interaction with clathrin-coated pits.

41 ecruitment of the receptor/cargo to clathrin-coated pits.

42 s, like microvilli, cell-cell junctions, and coated pits.

43 table endocytic vesicles arise from clathrin-coated pits.

44 that undergoes endocytosis through clathrin-coated pits.

45 mobility is restricted by interactions with coated pits.

46 dium, suggesting the involvement of clathrin-coated pits.

47 so found to enter the cell predominantly via coated pits.

48 mine the number of dynamins recruited to the coated pits.

49 VECs), increasing NP uptake through clathrin-coated pits.

50 to invagination and then fission of clathrin-coated pits.

51 e protein (WASP) assembles actin at clathrin-coated pits.

52 llularly into EEA-1+ endosomes from clathrin-coated pits.

53 T-1-HA-GFP internalization requires clathrin-coated pits.

54 mechanism for endocytosis involves clathrin-coated pits [1], but evidence has accumulated for additi

55 investigate the massive increase in clathrin-coated pit abundance that is selectively observed at a s

56 d to contribute to the formation of clathrin-coated pits, although the specific components that conne

57 d at the constricting neck of a fully formed coated pit and immediately after vesicle budding, accumu

58 GAK was disrupted showed a lack of clathrin-coated pits and a complete block in clathrin-mediated en

59 ults in an accumulation of arrested clathrin-coated pits and a greatly reduced synaptic vesicle numbe

60 n-mediated endocytosis with shallow clathrin-coated pits and a strong reduction in the internalizatio

61 interaction of DAT with adaptor proteins in coated pits and acceleration of DAT endocytosis.

62 th clathrin assembly into endocytic clathrin-coated pits and active Cdc42.

63 olocalizes with clathrin and AP2 in clathrin-coated pits and at the leading edge of migrating cells.

64 t OCRL visits late-stage, endocytic clathrin-coated pits and binds the Rab5 effector APPL1 on periphe

65 h receptor-mediated endocytosis via clathrin-coated pits and caveolae, that actin filaments and micro

66 hat is insensitive to inhibitors of clathrin-coated pits and caveolae.

67 e peptides inhibit the formation of clathrin-coated pits and coated vesicles during synaptic vesicle

68 or, which is highly concentrated at clathrin-coated pits and coordinates acquisition of bilayer curva

69 ution, we detected the arrival of dynamin at coated pits and defined dynamin dimers as the preferred

70 oblasts, these two receptors co-localized in coated pits and endosomal compartments following PDGF st

71 hway that involves the formation of clathrin-coated pits and fusion to early endosomes.

72 ich were concentrated at late-stage clathrin-coated pits and in lamellipodia, also dissociated from t

73 ARH colocalizes with megalin in clathrin coated pits and in recycling endosomes in the Golgi regi

74 NM23-H1/H2 localized at clathrin-coated pits and interacted with the proline-rich domain

75 te that E-selectin clusters in both clathrin-coated pits and lipid rafts of endothelial cells but is

76 Clathrin coated pits and numerous uncoated intracellular vesicles

77 t whether cortactin associates with clathrin-coated pits and participates in receptor-mediated endocy

78 distinct endocytic pathways (i.e., clathrin-coated pits and plasma membrane lipid rafts) that delive

79 7 is constitutively internalised by clathrin-coated pits and that physiological stimulators such as G

80 ution images of living cells, using clathrin-coated pits and the transferrin cargo as model systems.

81 rafficking; it is recruited to both clathrin-coated pits and to ensuing uncoated endocytic vesicles (

82 ane protein that is endocytosed via clathrin-coated pits and traffics through the acidic endosomes, t

83 d FcRY-mediated internalization via clathrin-coated pits and transport involving early and recycling

84 The lattices of clathrin-coated pits and vesicles are comprised of triskelions, e

85 in, and F-actin and increased the amounts of coated pits and vesicles at the apical plasma membrane.

86 ent Sec5 is unexpectedly present in clathrin-coated pits and vesicles at the plasma membrane.

87 Clathrin assembly into coated pits and vesicles is promoted by accessory protei

88 in heavy chain (Chc), a major constituent of coated pits and vesicles, is the most abundant protein c

89 e cellular machineries, such as the clathrin-coated pits and vesicles.

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

91 transmembrane proteins that are sorted into coated pits and vesicles.

92 selective increase in unconstricted clathrin-coated pits and, in the case of swinholide, an additiona

93 We propose that RME-4 functions on coated pits and/or vesicles to recruit RAB-35, which in

94 Ack is concentrated at clathrin-coated pits, and binds clathrin heavy chain via two clat

95 rotein required for the assembly of clathrin-coated pits, and DN PAK-1, an obligate mediator of macro

96 s from the plasma membrane, through clathrin-coated pits, and into the cell for lysosomal degradation

97 A associates with Arc, localizes to clathrin-coated pits, and is associated with endocytic sites in d

98 ents, three-dimensional tracking of clathrin-coated pits, and long-term imaging spanning >10 h and en

99 ternalization was also dependent on clathrin-coated pits, and Lp(a) was targeted for lysosomal and no

100 interacts with AP-2, is enriched on clathrin-coated pits, and requires clathrin but not RAB-5 for cor

101 to G proteins, internalization via clathrin-coated pits, and signaling via a growing list of "scaffo

102 tered into HRPTEC via caveolae, not clathrin-coated pits, and that BKV is maximally associated with c

103 re most likely internalized through clathrin-coated pits, and then returned to the plasma membrane vi

104 to be internalized independently of clathrin-coated pits, and there is evidence to suggest that lipid

105 reveal distinct mechanisms for sorting into coated pits, and thereby explain differential effects on

106 th clathrin and other components of clathrin-coated pits, AP-2 did not seem to be present in clathrin

107 Clathrin-coated pits are a major entry portal where assembled cla

108 We conclude that clathrin-coated pits are dynamic structures with rapid exchange o

109 rin in the cytosol, suggesting that clathrin-coated pits are dynamic structures.

110 naling, in cells in which endocytic clathrin-coated pits are frozen at a deeply invaginated state, th

111 Clathrin-coated pits are well defined, but the identity, mechanis

112 ciated endocytic adapters recruit cargoes to coated pits as a first step in endocytosis.

113 in multimolecular clusters unassociated with coated pits, as assessed by immuno-electron microscopy.

114 ucing GLUT1 internalization through clathrin-coated pits, as well as indirectly, by reducing the leve

115 Coated pits assemble by growth of a clathrin lattice, wh

116 Clathrin-coated pits assemble on a membrane and pinch off as coat

117 ro cells is slow, is independent of clathrin-coated-pit assembly, is dependent on an intact caveolin-

118 Clathrin-coated pits associated with the plasma membrane were sti

119 y a dominant negative mutant of the clathrin-coated pit-associated protein Eps15.

120 ved during recruitment of EGF receptors into coated pits at 4 degrees C and reached maximum at 37 deg

121 ors that had first been allowed to enter the coated pits at 4 degrees C.

122 ulation of clathrin, accessory proteins, and coated pits at the apical plasma membrane.

123 Despite the identification of clathrin-coated pits at the cell surface over 30 years ago, the f

124 Clathrin-coated pits at the cell surface select material for tran

125 ompound that induces misassembly of clathrin-coated pits at the cell surface.

126 mbles around the necks of deeply invaginated coated pits at the plasma membrane and catalyzes vesicle

127 he clathrin adaptors AP2 and AP1 in clathrin-coated pits at the plasma membrane and trans-Golgi netwo

128 etramers stimulates formation of constricted coated pits at the plasma membrane by regulating the cha

129 er photobleaching, that clathrin in clathrin-coated pits at the plasma membrane exchanges with free c

130 s with membranes, and the number of clathrin-coated pits at the plasma membrane increased when PIP2 i

131 the scission of deeply invaginated clathrin-coated pits at the plasma membrane, but the mechanisms g

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

133 hat both BRAG2 and Arf5 localize to clathrin-coated pits at the plasma membrane.

134 lathrin-coated vesicles, but not of clathrin-coated pits, at synapses.

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

136 ficantly affecting the structure of clathrin-coated pits, both clathrin and AP2 at the plasma membran

137 The latter suggests that coated pits bud from these regions.

138 a-arrestin directs the receptors to clathrin-coated pits but does not internalize with them.

139 e HCl, which blocks endocytosis via clathrin-coated pits, but not by nystatin and cholera toxin B, wh

140 orming a collar around the necks of clathrin-coated pits, but the specific structural interactions an

141 errin receptor is incorporated into clathrin-coated pits by associating, via tyrosine-based motifs, w

142 ctivated receptors are recruited to clathrin-coated pits by beta-arrestins, scaffolding proteins that

143 marked as cargo for inclusion into clathrin-coated pits by common internalization signals (e.g. YXXP

144 earchers to observe the dynamics of clathrin-coated pit (CCP) assembly in real time.

145 n 2 (AP2) complexes, which initiate clathrin-coated pit (CCP) assembly, are activated by conformation

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

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

148 hought to play an important role in clathrin-coated pit (CCP) dynamics.

149 arks the isolation of a cargo-laden clathrin-coated pit (CCP) from the cell exterior.

150 corresponded to a decreased rate of clathrin-coated pit (CCP) initiation and increased lifetimes of p

151 ACT: Some endocytic cargoes control clathrin-coated pit (CCP) maturation, but it is not known how suc

152 t of cargo molecules into a growing clathrin-coated pit (CCP).

153 (PTE), where it is concentrated in clathrin-coated pits (CCPs) and vesicles in the brush border regi

154 Clathrin-coated pits (CCPs) are generally considered a uniform po

155 l CME proceeds via the formation of clathrin-coated pits (CCPs) at the plasma membrane, which invagin

156 Clathrin-coated pits (CCPs) in proximity to substrate contacts ex

157 mediate assembly and maturation of clathrin-coated pits (CCPs) into cargo-containing vesicles.

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

159 observed heterogeneous dynamics of clathrin-coated pits (CCPs) might be the different cargo content.

160 tors, either recruiting cargos into clathrin-coated pits (CCPs) or initiating clathrin-coat assembly

161 fate by regulating the dynamics of clathrin-coated pits (CCPs) that mediate their internalization.

162 tures at the plasma membrane termed clathrin-coated pits (CCPs) that mediate vesicle formation.

163 ial increase in the ratio of "open" clathrin-coated pits (CCPs) to "necked"/"closed" CCVs and a doubl

164 on of the lifetime distributions of clathrin-coated pits (CCPs) to measure independent aspects of CCP

165 ls and is concentrated at endocytic clathrin-coated pits (CCPs) via interactions with the scaffold pr

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

167 e known to accumulate into maturing clathrin-coated pits (CCPs), whether and how cargo recruitment af

168 teraction of BMPRs with proteins in clathrin-coated pits (CCPs).

169 regulated by their endocytosis via clathrin-coated pits (CCPs).

170 nt of adaptors and clathrin to form clathrin-coated pits (CCPs).

171 at markedly affect the structure of clathrin-coated pits, clathrin exchange was blocked but AP2 at th

172 eractor, is recruited to late-stage clathrin-coated pits, clinical manifestations have been primarily

173 akdown on the dynamics of endocytic clathrin-coated pit components and of the actin regulatory comple

174 in (CL) and AP-2 components of the endocytic coated pit (CP).

175 Interestingly, recruitment of EGFR into coated pits did not require physiological temperature be

176 Capsids that did not encounter a coated pit dissociated from the cell surface with a half

177 they are recruited to a diffraction-limited coated pit during its assembly at the plasma membrane.

178 ates initially in the maturation of clathrin-coated pits during early stages of synaptic vesicle recy

179 this paper, we describe a study of clathrin-coated pit dynamics in living cells using ion conductanc

180 increased rates of CME and altered clathrin-coated pit dynamics.

181 ent endocytosis of heptahelical receptors in coated pits employs the clathrin adaptor beta-arrestin p

182 density lipoprotein (LDL) receptor (LDLR) in coated pits employs the clathrin adaptor protein ARH.

183 s and its metabolic processing, the clathrin-coated pit endocytosis pathway, and the ubiquitin/26 S p

184 , ARH and megalin are first seen in clathrin coated pits followed by sequential localization in early

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

186 sue culture-adapted strains utilize clathrin-coated pits for entry.

187 ional hot spots, from which large numbers of coated pits form and vesicles are generated.

188 uggest a role for synaptojanin 2 in clathrin-coated pit formation and imply that lipid hydrolysis is

189 efore function to initiate calcium-regulated coated pit formation at the cell surface or on intracell

190 nding domain of AP180, which blocks clathrin-coated pit formation but not clathrin-independent endocy

191 t for myosin VI in membrane invagination and coated pit formation in enterocytes.

192 imately 75 s, similar to the time scales for coated pit formation seen in cells.

193 clathrin-coated vesicle formation, including coated pit formation, constriction, and internalization.

194 Stationary coated pits formed and budded on the remainder of the do

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

196 e motifs that mediate EGFR interactions with coated pits have not been mapped.

197 is low-pH dependent occurs through clathrin-coated pits in a manner similar to wild-type virus.

198 A subpopulation of clathrin-coated pits in cell bodies and dendrites label for GluR2

199 ally believed that the formation of clathrin-coated pits in epithelial cells occurs randomly along th

200 , MORs are rapidly internalized via clathrin-coated pits in heterologous cells and dissociated striat

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

202 diated endocytosis, is recruited to clathrin-coated pits in two sequential phases.

203 remain defective in the scission of clathrin-coated pits in vivo.

204 The membrane of an assembling coated pit, in equilibrium with the surrounding plasma m

205 nt internalization, indicating that clathrin-coated pits, in concert with mechanisms dependent on raf

206 nvaginations accumulated, capped by clathrin-coated pits, in synapses of dynamin 1-knockout mice.

207 lly defined by the cytoskeleton and clathrin-coated pits, in which receptors and G proteins are confi

208 ccessory proteins typical of plasma membrane-coated pits, including AP2, AP180, and epsin, but not Hi

209 rafts, the actin cytoskeleton, and clathrin-coated pits influences B cell signaling and antigen pres

210 Our data lead to a model in which coated pits initiate randomly but collapse unless stabil

211 On U373 cells, coated pits initiated on the dorsal membrane at the fron

212 This objective picture of coated pit initiation also shows that methods outlined h

213 ce of molecular events required for clathrin-coated pit initiation.

214 Two types of coated pit intermediates accumulate during dynasore trea

215 uit and polymerize clathrin to form clathrin-coated pits into which cargo is sorted.

216 Clathrin-coated pits invaginate from specific membrane compartmen

217 on of the SNX9.dynamin-2 complex to clathrin-coated pits is blocked by interactions with the abundant

218 of G protein-coupled receptors via clathrin-coated pits is dependent on the adaptor protein beta-arr

219 mediated cholesterol uptake through clathrin-coated pits is now well understood, the molecular detail

220 hich to engage adaptors to recruit them into coated pits, is problematical; that of prion protein in

221 Coated pits, junctional complexes, desmosomes, and basem

222 olocalization of EGF-rhodamine conjugate and coated pits labeled with yellow-fluorescent-protein-tagg

223 15 is found at the growing edges of clathrin-coated pits, leading to the hypothesis that it participa

224 laterally diffused into assembling clathrin-coated pits less than 30 s after attachment.

225 microscopy, which revealed cadherin-enriched coated pit-like structures in close association with adh

226 We conclude that, in contrast to signals for coated pit localization that are in the cytoplasmic tail

227 and TGN46, but not the AP-2 plasma membrane-coated pit marker nor the endosomal markers EEA1, Hrs, a

228 of neutral sphingomyelinase but not clathrin-coated pit maturation.

229 The first is associated with coated pit maturation; the second, with fission of the m

230 ter that is a critical component of clathrin-coated pit-mediated endocytosis, as well as in stress re

231 h chase and became undetectable if clathrin-coated pit-mediated trafficking was blocked with chlorpr

232 ature and mature DCs are capable of clathrin-coated pit-mediated uptake of SIV, supporting the notion

233 om the circulatory and lymphatic systems via coated pit-mediated uptake.

234 and-bound EGFR is incorporated into clathrin-coated pits--membrane structures containing clathrin and

235 the receptors can exhibit mean lifetimes in coated pits much shorter than the lifetime of the pit at

236 Coated pits near synapses typically lack GluR2 label und

237 sensors, disappearance of endocytic clathrin-coated pits, nearly complete inhibition of KCNQ2/3 chann

238 vate the concentration of PtdIns(4,5)P(2) at coated pit necks, and effectively cluster (or sequester)

239 t a model in which endophilin recruitment to coated pit necks, because of its curvature-sensing prope

240 ns facilitate cargo recruitment and clathrin-coated pit nucleation.

241 ndocytosis through the formation of clathrin-coated pits on the cell membrane.

242 microscopy to study the assembly dynamics of coated pits on the dorsal and ventral membranes of migra

243 tors are delivered selectively from clathrin-coated pits on the plasma membrane into a specific subpo

244 complex accumulates at a subset of clathrin-coated pits on the surface of human cells.

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

246 No clathrin-coated pits or vesicles could be detected in the clathri

247 desialylated glycoproteins via the clathrin-coated pit pathway and mediates their delivery to lysoso

248 ming that uptake is mediated by the clathrin-coated pit pathway.

249 and processed normally through the clathrin-coated pit pathway.

250 rnalized, predominantly through the clathrin-coated pit pathway.

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

252 on, up to a final value of 30 nm just before coated-pit pinching and formation of the coated vesicle.

253 clathrin/AP-2 puncta may represent loci for coated pit production and that previous models that assu

254 le TGF-beta receptors to AP2 and to clathrin-coated pits, providing the first in vivo evidence for in

255 A large fraction of budding coated pits recruit between 26 and 40 dynamins (between

256 eceptor kinase is essential for the initial, coated pit recruitment step of endocytosis.

257 ite may represent receptor interactions with coated-pit regions in the cell membrane or with other ce

258 okine receptors internalize through clathrin-coated pits, regulation of the receptor trafficking is n

259 to coordinate cargo selection into clathrin-coated pits, results in a significant impairment in endo

260 ansmembrane receptors requires that clathrin-coated pits retain the receptors long enough to allow ve

261 vity, and axonal boutons containing clathrin-coated pits showed a more pronounced decrease in presyna

262 t due to failure of receptors to localize in coated pits since the number of LDLRs in coated pits was

263 the recruitment of P-selectin into clathrin-coated pits, slowed the internalization of P-selectin, a

264 nd it remains controversial whether clathrin-coated pits specialize to internalize particular recepto

265 e cells (untreated or treated to alter their coated pit structure), we demonstrated that their mobili

266 ment of adaptor proteins present in clathrin-coated pits, such as epsin, Eps15 (epidermal growth fact

267 enrichment of LDLR-Y807C-bound beta-VLDL in coated pits, suggesting that beta-VLDL binding promoted

268 QHF, and NPLY) provide redundancy to mediate coated pit targeting and endocytosis of HARE.

269 Dab2 colocalizes with integrin beta1 in coated pits that are dispersed over the cell surface, su

270 ted DSL proteins to a particular subclass of coated pits that have special properties essential for N

271 t burst of EGFP-SNX9 recruitment to clathrin-coated pits that occurs during the late stages of vesicl

272 lin is required for constriction of clathrin-coated pits, the same early step in endocytosis known to

273 en as the cargoes being enclosed in clathrin-coated pits, they slow down the active rotation and expe

274 an adaptor that couples late-stage endocytic coated pits to actin polymerization and which we found t

275 eveal a link between progression of clathrin-coated pits to endocytic vesicles and an activation-deac

276 nd hence in oocytes is recruited to clathrin-coated pits to facilitate the rapid recycling of Yolkles

277 indings indicate that BRAG2 acts at clathrin-coated pits to promote integrin internalization by activ

278 bsence of SCAR, some WASP relocated from the coated pits to the leading edge, where it behaved with s

279 5 that is an essential component of clathrin-coated pits, to investigate the extent and importance of

280 is of ligand-receptor complexes via clathrin-coated pits, trafficking of the internalized ligand to l

281 ted endocytosis and associates with clathrin-coated pits/vesicles at the plasma membrane.

282 cells, LKT moves to lipid rafts and clathrin-coated pits via a dynamic process that results in LKT in

283 because the maximal accumulation of EGFR in coated pits was observed at 4 degrees C.

284 in coated pits since the number of LDLRs in coated pits was similar in ARH-/- and normal cells.

285 INPP5B visits late stage endocytic clathrin-coated pits, was earlier shown to contain another bindin

286 ivated PAR1 internalization through clathrin-coated pits we examined the function of a highly conserv

287 s they were swept back toward the cell body; coated pits were absent from the corresponding ventral m

288 did not show any sign of a protein coat, and coated pits were not detected.

289 h encodes a protein associated with clathrin-coated pits where cell-surface receptors reside.

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

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

292 omplex with the GTPase dynamin-2 at clathrin-coated pits, where it provokes fission of vesicles to co

293 e at the base of arrested endocytic clathrin-coated pits, where they support the growth of dynamic lo

294 ith PD158780 prevented EGFR recruitment into coated pits, whereas the inhibitor did not block the int

295 nternalized, P-selectin clusters in clathrin-coated pits, which enhances its ability to support leuko

296 esicles and an increase in U-shaped clathrin-coated pits, which may result from sequestration of coat

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

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

299 and is thought to coordinate constriction of coated pits with membrane fission (via dynamin) and subs

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