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

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

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

5 between certain transmembrane receptors and detergent-resistant membranes.

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

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

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

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

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

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

12 than is predicted by biochemical analysis of 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 f PIP(2) from detergent-soluble membranes to detergent-resistant membranes by -1.3 kcal/mol.

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

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

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

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

33 Detergent-resistant membranes contain signaling and inte

34 Isolated detergent-resistant membranes contain Src and PLCgamma,

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

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

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

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

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

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

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

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

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

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

45 18L) and MEC-2(P134S) did not fractionate in detergent-resistant membrane domains.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

103 -33 protein is partially associated with the detergent-resistant membrane fraction.

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

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

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

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

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

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

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

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

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

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

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

115 2R structures were significantly denser than detergent-resistant membrane fragments containing flotil

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

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

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

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

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

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

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

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

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

125 2B4 phosphorylation and 2B4 association with detergent-resistant membranes, indicating that inhibitor

126 Furthermore, detergent-resistant membranes isolated by sucrose gradie

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

128 Detergent-resistant membranes isolated from rod outer se

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

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

131 Detergent-resistant membranes made from the same cells s

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

133 Detergent-resistant membrane microdomains (DRM) rich in

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

157 1 and TORC2 fractionate with a novel form of detergent-resistant membranes that are distinct from det

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

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

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

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

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

163 Equivocally, detergent-resistant membranes were initially assumed to

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

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

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

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

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