ライフサイエンスコーパス: detergent-resistant membrane

1 ads1- grew well and maintained lipid rafts (detergent-resistant membranes).

2 than is predicted by biochemical analysis of detergent-resistant membranes.

3 h no change in the amount of NHE3 in the BBM detergent-resistant membranes.

4 A, NS5B, and NS3, were also localized to the detergent-resistant membranes.

5 ne domain of HA facilitated binding of M1 to detergent-resistant membranes.

6 between certain transmembrane receptors and detergent-resistant membranes.

7 , which was exemplified by the disruption of detergent-resistant membranes.

8 omain (MBD), which both mediate targeting to detergent-resistant membranes.

9 the extent of lipid probe partitioning into detergent-resistant membranes.

10 hiDISCs are found both inside and outside of detergent-resistant membranes.

11 f the released 3a protein is associated with detergent-resistant membranes.

12 lasma membrane domains and fractionates with detergent-resistant membranes.

13 and cell fractions, including endosomes and detergent-resistant membranes, 1622 phosphorylated prote

14 ulation of the anandamide carrier protein in detergent-resistant membranes after dynamin 2 knockdown.

15 some of the protein remains associated with detergent-resistant membranes, also termed lipid rafts,

16 ) fractions, whereas AQP-0 was found in both detergent resistant membrane and DSM fractions.

17 nd CNTNAP1 associate with gamma-secretase in detergent-resistant membranes and affect APP processing

18 a and caveolin-1 occurs in cholesterol-rich, detergent-resistant membranes and is likely to be depend

19 ates the interaction of alpha-synuclein with detergent-resistant membranes and reveals a shift in ele

20 PMA, but not DiC8, targeted PKCalpha to detergent-resistant membranes, and disruption of these d

21 A subset of apical proteins partition into detergent-resistant membranes, and the association of th

22 HN, M, and F(1)/F(2) are associated with detergent-resistant membranes, and these proteins float

23 ion at the plasma membrane, association with detergent-resistant membranes, and vesicular release of

24 e BBM detergent-soluble fraction but not the detergent-resistant membrane; and (3) the molecular leve

25 MAL is a detergent-resistant membrane-associated protein implicat

26 We find that MAL is not involved in detergent-resistant membrane association or apical deliv

27 tely 50% of the protein was sequestered into detergent resistant membranes at a 1:100 ratio, where fr

28 t that beta1 integrins regulate the level of detergent-resistant membrane at the plasma membrane in a

29 f PIP(2) from detergent-soluble membranes to detergent-resistant membranes by -1.3 kcal/mol.

30 ince: (1) c-Src was rapidly activated in the detergent-resistant membranes by carbachol; and (2) carb

31 t widely used biochemical approaches such as detergent-resistant membranes cannot resolve this biolog

32 nucleus of TCCSUP bladder cancer cells to a detergent-resistant membrane compartment, where the grow

33 on of Igalpha/Igbeta-containing complexes to detergent-resistant membrane compartments is absolutely

34 y accumulates in intracellular Xfect-induced detergent-resistant membrane compartments which appear t

35 Detergent-resistant membranes contain signaling and inte

36 Isolated detergent-resistant membranes contain Src and PLCgamma,

37 ein, or transferrin receptor, accumulated in detergent-resistant membranes containing GM1.

38 stranded RNA in addition to being present in detergent-resistant membranes containing NS5A.

39 rain failed to reduce CD40 relocation to the detergent-resistant membrane domain and to inhibit CD40-

40 es the reorganization of CD11b integrin into detergent resistant membrane domains; in turn, CD11b rec

41 nstrate that E1* associated selectively with detergent-resistant membrane domains (DRMs or rafts).

42 luster PM-derived cholesterol into transient detergent-resistant membrane domains (DRMs) within the E

43 ophil plasma membrane becomes organized into detergent-resistant membrane domains (DRMs), the distrib

44 tor complex and the cholesterol are found in detergent-resistant membrane domains that encompass a la

45 Isolated caveolae/lipid raft-enriched detergent-resistant membrane domains were prepared using

46 ding p53/56lyn and several other markers for detergent-resistant membrane domains, as well as an inte

47 Detergent-resistant membrane domains, into which GPI-lin

48 ly for FcepsilonRI that associate with these detergent-resistant membrane domains, which are enriched

49 18L) and MEC-2(P134S) did not fractionate in detergent-resistant membrane domains.

50 1 proteins resulted in gD fractionation into detergent resistant membranes (DRM) and that gD co-local

51 uantify >100 phospholipid (PL) components in detergent-resistant membrane (DRM) domains that are rela

52 he Sema3E tripartite receptor complex within detergent-resistant membrane (DRM) domains, and DRM doma

53 show that leukocyte PECAM translocates to a detergent-resistant membrane (DRM) during transmigration

54 Vav1 was recruited to a detergent-resistant membrane (DRM) fraction only when 2B

55 also showed the enrichment of sterols in the detergent-resistant membrane (DRM) fractions obtained fr

56 mmunological synapse and its localization in detergent-resistant membrane (DRM) fractions were defect

57 ng BIG/TIR3 and partitions into Triton X-100 detergent-resistant membrane (DRM) fractions.

58 sulted in a strong decrease of the amount of detergent-resistant membrane (DRM) material.

59 on, facilitates the dispersion of FGFR2 into detergent-resistant membrane (DRM) micro-domains.

60 cytes, proteins associated with host-derived detergent-resistant membrane (DRM) rafts are selectively

61 hrombin translocated immediately in platelet detergent-resistant membrane (DRM) rafts but that from G

62 Highlights include a demonstration that (1) detergent-resistant membrane (DRM) rafts exist in the re

63 Studies of detergent-resistant membrane (DRM) rafts in mature eryth

64 Photoreceptor membranes contain detergent-resistant membrane (DRM) rafts.

65 biosensor, and target it into or outside of detergent-resistant membrane (DRM) regions at the plasma

66 talizes exclusively to caveolin-1-associated detergent-resistant membrane (DRM) vesicles in HT-29 cel

67 K6 protein was enriched in the detergent-resistant membrane (DRM), a key site of Src in

68 um signaling to mitochondria, is enriched in detergent-resistant membrane (DRM)-forming lipids, inclu

69 termed lipid rafts, which can be isolated as detergent-resistant membrane (DRM).

70 by three different techniques to produce (i) detergent-resistant membranes (DRM) and detergent-solubl

71 ation between NS2 and E2 localization to the detergent-resistant membranes (DRM) and HCV particle ass

72 mast cells results in its co-isolation with detergent-resistant membranes (DRM) and its consequent t

73 says to demonstrate that NS2 associates with detergent-resistant membranes (DRM) in a p7-dependent ma

74 certain ER-directed toxins and viruses with detergent-resistant membranes (DRM) may provide a genera

75 Lipid rafts, also known as detergent-resistant membranes (DRM), are microdomains in

76 ) to the virus assembly sites located at the detergent-resistant membranes (DRM).

77 r and phase behavior and by the formation of detergent-resistant membranes (DRM).

78 A subset of these detergent-resistant membranes (DRM-H) exhibits a higher

79 ng to detergent soluble membranes (DSMs) and detergent resistant membranes (DRMs) from 1:1:1 PC:SM:ch

80 " have been isolated from many cell types as detergent-resistant membranes (DRMs) and are enriched in

81 oduced lysoGPI-APs are not incorporated into detergent-resistant membranes (DRMs) but still are deliv

82 t isolated and determined the composition of detergent-resistant membranes (DRMs) from chondrocyte PM

83 Immunosera raised against detergent-resistant membranes (DRMs) from monocytes or a

84 In recent years, detergent-resistant membranes (DRMs) have been isolated

85 V replicons is biochemically associated with detergent-resistant membranes (DRMs) in a manner similar

86 tions were isolated and purified as buoyant, detergent-resistant membranes (DRMs) in OptiPrep density

87 l-rich membrane domains, its localization in detergent-resistant membranes (DRMs) in transfected cell

88 We found that GAP-43 was enriched in detergent-resistant membranes (DRMs) isolated by Triton

89 The dynamic structure of detergent-resistant membranes (DRMs) isolated from RBL-2

90 Here we report that the detergent-resistant membranes (DRMs) play an important r

91 Proteomic analysis of detergent-resistant membranes (DRMs) revealed that the g

92 Gag precursors partly associate with detergent-resistant membranes (DRMs) that are believed t

93 ed and cytoplasmic proteins, associated with detergent-resistant membranes (DRMs) that are characteri

94 A protocol to prepare Triton X-100 detergent-resistant membranes (DRMs) was developed using

95 ated detergent-soluble membranes (DSMs) from detergent-resistant membranes (DRMs), and measured their

96 viral proteins in lipid rafts, as defined by detergent-resistant membranes (DRMs), in non-lipid raft

97 phatidylinositol-anchor that associates with detergent-resistant membranes (DRMs), or rafts.

98 orylation of caveolin-2 preferably occurs in detergent-resistant membranes (DRMs), while serine 36 ph

99 f 4 host proteins that reside in erythrocyte detergent-resistant membranes (DRMs).

100 of cell-associated toxin was associated with detergent-resistant membranes (DRMs).

101 membrane binding and localization of Fyn to detergent-resistant membranes (DRMs).

102 Rafts were isolated from cell lysates as detergent-resistant membranes (DRMs).

103 lated with its inability to translocate into detergent-resistant membranes (DRMs).

104 oscopic examination, and by association with detergent-resistant membranes (DRMs).

105 h Triton X-100-insoluble membrane fragments (detergent-resistant membranes, DRMs) containing lipids i

106 at was found to be associated with raft-rich detergent-resistant membranes exceeded DHA by almost a f

107 chimeras induced toxicity, fractionated with detergent-resistant membranes extracted from toxin-treat

108 ned 'lipid rafts' as defined by Triton X-100 detergent resistant membrane formation.

109 eliminated the association of ULBP1 with the detergent-resistant membrane fraction and caused a signi

110 Although CFTR has been detected in a detergent-resistant membrane fraction prepared from airw

111 ss the 2B4 ligand, is found exclusively in a detergent-resistant membrane fraction that contains lipi

112 -33 protein is partially associated with the detergent-resistant membrane fraction.

113 he I domain is required for interaction with detergent-resistant membrane fractions (DRMs).

114 ns, experimentally also termed mitochondrial detergent-resistant membrane fractions (mDRM), play a ro

115 Recruitment of 2B4 into detergent-resistant membrane fractions and 2B4 phosphory

116 nt differences in the protein composition of detergent-resistant membrane fractions from wildtype and

117 cells, the association of Fc(epsilon)RI with detergent-resistant membrane fractions is inhibited by 1

118 C162A modulated sodium current and sorted to detergent-resistant membrane fractions normally.

119 , the association of Kv1.5 with low-density, detergent-resistant membrane fractions requires coexpres

120 A subset of EWRS1 translocates into detergent-resistant membrane fractions, which contain th

121 atalyzes Nephrin phosphorylation in podocyte detergent-resistant membrane fractions.

122 phrin phosphorylation in isolated glomerular detergent-resistant membrane fractions.

123 Podocin, Neph1 was enriched in Triton X-100 detergent-resistant membrane fractions.

124 ent in which the EGF receptor is retained in detergent-resistant membrane fractions.

125 utrophils co-isolates with cholesterol-rich, detergent-resistant membrane fragments (DRMs) that exhib

126 2R structures were significantly denser than detergent-resistant membrane fragments containing flotil

127 ed sterol-dependent proteins associated with detergent resistant membranes from Arabidopsis thaliana

128 novel gamma-secretase-associated proteins in detergent-resistant membranes from brain.

129 Chemical cross-linking of detergent-resistant membranes from rat MV indicates that

130 PDGFRalpha is less associated with detergent-resistant membranes in ASA-deficient cells and

131 rdered domain model explains the behavior of detergent-resistant membranes in liposomes and cells.

132 D, and there is less Pr65gag associated with detergent-resistant membranes in mutant-infected cells.

133 ion proteins are associated with sterol-rich detergent-resistant membranes in yeast and plant cells.

134 endocytic recycling compartment has abundant detergent-resistant membranes, in contrast to the late e

135 Ralpha levels, corrected its localization to detergent-resistant membranes, increased AKT phosphoryla

136 2B4 phosphorylation and 2B4 association with detergent-resistant membranes, indicating that inhibitor

137 Furthermore, detergent-resistant membranes isolated by sucrose gradie

138 nity purification, and immunopurification of detergent-resistant membranes isolated from CACO-2BBE ce

139 Detergent-resistant membranes isolated from rod outer se

140 ee affinity chromatography and compared with detergent-resistant membranes isolated from the same cel

141 erol in cell membranes, was not found within detergent-resistant membranes (lipid rafts), and did not

142 Detergent-resistant membranes made from the same cells s

143 s in a large scale proteomic quantitation of detergent resistant membrane microdomains (DRMMs) isolat

144 Detergent-resistant membrane microdomains (DRM) rich in

145 t) cells were incubated with Ib, after which detergent-resistant membrane microdomains (DRMs) were ex

146 Hsp70, the same proteins that associate with detergent-resistant membrane microdomains (DRMs), which

147 Np) when added to cultured cells or purified detergent-resistant membrane microdomains containing Shh

148 an endocytic process that is associated with detergent-resistant membrane microdomains or lipid rafts

149 lasma membrane components are organized into detergent-resistant membrane microdomains referred to as

150 roteins that generally reside in specialized detergent-resistant membrane microdomains, act as signal

151 n of the immunological synapse by recruiting detergent-resistant membrane microdomains, termed lipid

152 C class II molecules (MHC-II) associate with detergent-resistant membrane microdomains, termed lipid

153 ctivities are present in caveolin-1-enriched detergent-resistant membrane microdomains.

154 pendent signaling events are associated with detergent-resistant membrane microdomains.

155 We demonstrate that detergent-resistant membrane nanodomains, also known as

156 HCV) replication complex is localized within detergent-resistant membranes or lipid rafts.

157 ylinositol (GPI) anchor that associates with detergent-resistant membranes, or rafts.

158 subunitsBandCand preserving the integrity of detergent-resistant membrane organization.

159 s of solubilized membranes to associate with detergent-resistant membranes present in separate bilaye

160 large fraction of PIP(2) associates with the detergent-resistant membrane "raft" fraction, but the fu

161 plasma membrane of mammalian cells contains detergent-resistant membrane rafts enriched in glycosphi

162 we show that their plasma membranes contain detergent-resistant membrane rafts that constitute a sma

163 g that palmitoylation does not target CPD to detergent-resistant membrane rafts.

164 oylation levels correlated with targeting to detergent-resistant membranes (rafts) and to caveolin-1.

165 d they also mean that cholesterol-containing detergent-resistant membrane remnants cannot correspond

166 e HCV RNA replication complex on lipid raft (detergent-resistant membranes) requires interactions amo

167 icknesses of detergent soluble membranes and detergent resistant membranes, respectively, are both lo

168 1 and TORC2 fractionate with a novel form of detergent-resistant membranes that are distinct from det

169 ls and also disrupts those interactions with detergent-resistant membranes that are isolated by sucro

170 es in low-buoyant-density, cholesterol-rich, detergent-resistant membranes that can be disrupted by c

171 peptide and PIP(2) were greatly enriched in detergent-resistant membranes that correspond to rafts;

172 We confirmed that this loss of detergent-resistant membrane was due to the lack of palm

173 s indicate that localization of Galpha(s) to detergent-resistant membranes was not required for G(s)

174 Equivocally, detergent-resistant membranes were initially assumed to

175 In addition, these detergent-resistant membranes were not enriched in arach

176 Both also associate with detergent-resistant membranes where viral replication co

177 arlier reported preferential localization to detergent-resistant membranes, where it is anchored via

178 HtrA from cellular lysates partitioned into detergent-resistant membranes, which contain cholesterol

179 ctively, in the amount of Galpha(s) from the detergent-resistant membranes without any change in the