ライフサイエンスコーパス: vesicle-associated membrane protein

1 One major target of cytoplasmic Rbfox1 is vesicle associated membrane protein 1 (Vamp1).

2 3 deletion reduced hippocampal expression of vesicle-associated membrane protein 1 (VAMP1), a GABAerg

3 Vesicle associated membrane protein 2 (VAMP2/synaptobrev

4 The vesicle SNARE proteins VAMP2 (vesicle associated membrane protein 2) and VAMP3 mediate

5 Previous studies have demonstrated roles for vesicle-associated membrane protein 2 (VAMP 2) and VAMP

6 of multimeric protein complexes that include vesicle-associated membrane protein 2 (VAMP-2) and the p

7 tured neurotoxin with full-length substrates vesicle-associated membrane protein 2 (VAMP-2), synaptos

8 A stable ternary complex formed with vesicle-associated membrane protein 2 (VAMP2) and plasma

9 y bound to the SNARE-protein synaptobrevin-2/vesicle-associated membrane protein 2 (VAMP2) and promot

10 th a genome-wide shRNA screen, we identified vesicle-associated membrane protein 2 (VAMP2) as a criti

11 associates with synaptophysin in vivo after vesicle-associated membrane protein 2 (VAMP2) enters the

12 Synaptobrevin/vesicle-associated membrane protein 2 (VAMP2) is an esse

13 This requires nephrin, which interacts with vesicle-associated membrane protein 2 (VAMP2) on GLUT4 s

14 We reveal that vesicle-associated membrane protein 2 (VAMP2) orchestrat

15 kDa (SNAP-25) interacts with syntaxin 1 and vesicle-associated membrane protein 2 (VAMP2) to form a

16 ntified SV2, synaptotagmin I, synaptophysin, vesicle-associated membrane protein 2 (VAMP2), and the v

17 function also blocked distal localization of vesicle-associated membrane protein 2 (VAMP2), which is

18 ere we show that the juxtamembrane region of vesicle-associated membrane protein 2 (VAMP2)-a componen

19 both Vegfa loss-of-function and blockage of vesicle-associated membrane protein 2 (VAMP2)-dependent

20 live hippocampal nerve terminals expressing vesicle-associated membrane protein 2 (VAMP2)-pHluorin w

21 t-SNAREs 1B (VTI1B), Syntaxin 8 (STX8), and Vesicle-Associated Membrane Protein 2 (VAMP2).

22 naptosome-associated protein 23 (SNAP23) and vesicle-associated membrane protein 2 (VAMP2).

23 d a SNARE protein involved in GH exocytosis, vesicle-associated membrane protein 2 (VAMP2).

24 pins) and the native transmembrane domain of vesicle-associated membrane protein 2 (VAMP2).

25 assay revealed pairwise interactions between vesicle-associated membrane protein 2 and Syp and V-ATPa

26 Vesicle-associated membrane protein 2 colocalized to bot

27 rain extracts is promoted by dissociation of vesicle-associated membrane protein 2 from synaptophysin

28 docrine tissues, pantophysin associated with vesicle-associated membrane protein 2 in adipocytes.

29 t with the interaction of synaptophysin with vesicle-associated membrane protein 2 in neuroendocrine

30 replace the C-terminus of the SNARE motif of vesicle-associated membrane protein 2 in the four-helix

31 factor attachment receptor) proteins VAMP2 (vesicle-associated membrane protein 2) and syntaxin 4 (S

32 tein receptor) proteins: synaptobrevin 2 (or vesicle-associated membrane protein 2) on the synaptic v

33 tatory amino acid transporter 5), and VAMP2 (vesicle-associated membrane protein 2), are markedly red

34 onal interaction with synaptobrevin-2/VAMP2 (vesicle-associated membrane protein 2), leading to SNARE

35 some-associated protein of 25 kD) and VAMP2 (vesicle-associated membrane protein 2), precludes the in

36 eimide-sensitive fusion protein) and VAMP-2 (vesicle-associated membrane protein 2), stearoyl CoA des

37 metallothionein-2, creatine kinases B-type, vesicle-associated membrane protein 2, neurofilament lig

38 f botulinum toxin in AgRP neurons to prevent vesicle-associated membrane protein 2-dependent vesicle

39 wth factor receptor, syntrophin alpha 1, and vesicle-associated membrane protein 2.

40 NARE complex comprised of SNAP25/syntaxin 13/vesicle-associated membrane protein 2.

41 Together with vesicle-associated membrane protein-2 (VAMP-2) and synta

42 t protein receptors (SNAREs) cellubrevin and vesicle-associated membrane protein-2 (VAMP-2) and the t

43 ts spastic paralysis through the cleavage of vesicle-associated membrane protein-2 (VAMP-2) in neuron

44 ntaining diffuse staining for the prS marker Vesicle-Associated Membrane Protein-2 and (c) budding of

45 Finally, we show that vesicle-associated membrane protein-2 and synaptosome-as

46 as the secretory organelle membrane proteins vesicle-associated membrane protein-2 and synaptotagmin

47 that TAT-SNAP-23 bound to the combination of vesicle-associated membrane protein-2 and syntaxin-4 but

48 tion by live-cell imaging of pHluorin-VAMP2 (vesicle-associated membrane protein-2), a pH-sensitive-G

49 either the 31-kDa subunit of H(+)-ATPase or vesicle-associated membrane protein-2, co-immunoprecipit

50 eaction we identified transcripts for rab3a, vesicle-associated membrane protein-2, synaptosome-assoc

51 parations contain rab3a and SNARE, including vesicle-associated membrane protein-2, syntaxin-4, synap

52 TeNT cleaves vesicle-associated membrane protein-2, which inhibits ne

53 ptosome-associated protein-23, syntaxin, and vesicle-associated membrane protein-2.

54 rotein receptor (v-SNARE) called cellubrevin/vesicle-associated membrane protein-3 (VAMP-3) in platel

55 TP vesicular transport and fusion, including vesicle-associated membrane protein-3 and vesicular nucl

56 separate variants that preferentially cleave vesicle-associated membrane protein 4 (VAMP4) and Ykt6,

57 attachment protein receptor (SNARE) molecule vesicle-associated membrane protein 4 (VAMP4) as a key c

58 estigate the role of the di-leucine motif of vesicle-associated membrane protein 4 (VAMP4) in adaptor

59 s setting, we examined the potential role of vesicle-associated membrane protein 4 (VAMP4), a vesicul

60 -Golgi SNARE and syntaxin 6-binding partner, vesicle-associated membrane protein 4 (VAMP4), at the ch

61 nsitive factor attachment protein receptor), vesicle-associated membrane protein 4 (VAMP4), on SVs is

62 plexes with the endosomal arginine (R)-SNARE vesicle-associated membrane protein 4 (VAMP4).

63 naptosome-associated protein 29 (SNAP29) and vesicle-associated membrane protein 7 (VAMP7) in situ, h

64 reased association of SNAP23, Syntaxin4, and vesicle-associated membrane protein 7 (VAMP7) is detecte

65 SNAREs Vps10p-tail-interactor-1a (vti1a) and vesicle-associated membrane protein 7 (VAMP7) to specifi

66 or budding from the ER membrane and contains vesicle-associated membrane protein 7, found in intestin

67 Previous work suggested that human VAMP-7 (vesicle-associated membrane protein-7) was a SNARE requi

68 one of these genes, VAMP721a, which encodes vesicle-associated membrane protein 721a.

69 Autophagy Modulator 1 (DRAM1) interacts with Vesicle Associated Membrane Protein 8 (VAMP8) to mediate

70 Vesicle-associated membrane protein 8 (VAMP8) localizes

71 cular mechanisms, we examined platelets from vesicle-associated membrane protein 8 (VAMP8) null mice.

72 eracts with autophagy related 14 (ATG14) and vesicle-associated membrane protein 8 (VAMP8) through it

73 e investigated whether overexpression of the vesicle-associated membrane protein 8 (VAMP8), an R-SNAR

74 and SNAP29, and the vesicle (v)-SNARE VAMP8 (vesicle-associated membrane protein 8).

75 18 not only interacted with Syntaxin (Syn)7, vesicle-associated membrane protein 8, and Vti1-b but al

76 med complexes with syntaxin-11, SNAP-23, and vesicle-associated membrane protein-8 in human platelets

77 P-25) family helices, and an arginine (R) in vesicle-associated membrane protein (a 3Q:1R ratio).

78 Tetanus toxin cleaved platelet vesicle-associated membrane protein and inhibited Ca2+-i

79 Furthermore, two of these SNAREs, vesicle-associated membrane protein and syntaxin 3, were

80 econdensation, with the unusual retention of vesicle-associated membrane protein and the perinuclear

81 s was dependent on tetanus toxin-insensitive vesicle-associated membrane proteins and calcium mobiliz

82 nd tensin homolog (PTEN) and its ceRNA VAMP (vesicle-associated membrane protein)-associated protein

83 cell imaging results indicated that CaSR and vesicle-associated membrane protein-associated A (VAPA)

84 found the interaction between NS5A and human vesicle-associated membrane protein-associated protein A

85 hybrid screen identified the SNARE regulator vesicle-associated membrane protein-associated protein A

86 ndoplasmic reticulum membrane protein VAP-A (vesicle-associated membrane protein-associated protein A

87 1 (Bin1, also known as amphiphysin II), and vesicle-associated membrane protein-associated protein A

88 cell receptor-associated protein 31 (BAP31), vesicle-associated membrane protein-associated protein A

89 vity and was constitutively colocalized with vesicle-associated membrane protein-associated protein A

90 Vesicle-associated membrane protein-associated protein B

91 binding partner for the resident ER protein vesicle-associated membrane protein-associated protein B

92 ia interactions between the ER protein VAPB (vesicle-associated membrane protein-associated protein B

93 protein 5) and the ER-resident protein VAPB (vesicle-associated membrane protein-associated protein B

94 Vesicle-associated membrane protein-associated protein B

95 gh transgenic mice overexpressing the mutant vesicle-associated membrane protein-associated protein B

96 Proline with Serine at residue 56 (P56S) of vesicle-associated membrane protein-associated protein B

97 titution at position 56 in the gene encoding vesicle-associated membrane protein-associated protein B

98 titution at position 56 in the gene encoding vesicle-associated membrane protein-associated protein B

99 We find that VAP, the vesicle-associated membrane protein-associated protein i

100 gue of the integral ER membrane protein VAP (vesicle-associated membrane protein-associated protein)

101 d hVAP-33 (the human homologue of the 33-kDa vesicle-associated membrane protein-associated protein),

102 increasing NS5A interaction with the 33-kDa vesicle-associated membrane protein-associated protein.

103 ction with the human homologue of the 33-kDa vesicle-associated membrane protein-associated protein.

104 ls with endoplasmic reticulum (ER)-localized vesicle-associated membrane protein-associated proteins

105 d together by a tethering complex of VAPA/B (vesicle-associated membrane protein-associated proteins

106 iculum (ER) forms many MCS via two proteins, vesicle-associated membrane protein-associated proteins

107 otein, NET3C, and phylogenetically conserved vesicle-associated membrane protein-associated proteins

108 xtended synaptotagmins), and Scs2 and Scs22 (vesicle-associated membrane protein-associated proteins)

109 AT motif with endoplasmic reticulum-resident vesicle-associated membrane protein-associated proteins.

110 Mutations in the gene encoding vesicle-associated membrane protein B (VAPB) cause a fam

111 c lateral sclerosis (ALS)-causing variant of vesicle-associated membrane protein B (VAPB) in fly neur

112 We also synthesized a VAMP (vesicle-associated membrane protein)-based peptide conta

113 platelets with an antibody directed against vesicle-associated membrane protein completely inhibited

114 syntaxin-1, SNAP-25, and synaptobrevin/VAMP (vesicle-associated membrane protein) constitute the core

115 iated through NSF/GluR2 interactions but not vesicle-associated membrane protein-dependent exocytosis

116 isassemble the 20S complex and did not allow vesicle-associated membrane protein dissociation to any

117 n events involve members of the syntaxin and vesicle-associated membrane protein families.

118 ogen granules (ZG) express 2 isoforms of the vesicle-associated membrane protein family (VAMP2 and -8

119 cle protein synaptobrevin (also called VAMP, vesicle-associated membrane protein) forms part of the S

120 of a large number of different syntaxin and vesicle-associated membrane protein genes.

121 oluble form of the green fluorescent protein/vesicle-associated membrane protein (GFP-VAMP) was bound

122 FM dyes, VAMP (vesicle-associated membrane protein)-GFP (green fluoresc

123 RE proteins, secretory protein (MoSec22) and vesicle-associated membrane protein (MoVam7), as being i

124 Synaptobrevins or VAMPs are vesicle-associated membrane proteins, often called v-SNA

125 otagmin binding overlap with the domains for vesicle-associated membrane protein (or VAMP) and alpha-

126 icles are capable of docking even when VAMP (vesicle-associated membrane protein) or syntaxin is clea

127 SNAP-25, and synaptobrevin-2 (also known as vesicle-associated membrane protein, or VAMP-2) bind to

128 By contrast, vesicle-associated membrane protein peptides could not r

129 y inhibitory interneurons with cleavage of a vesicle-associated membrane protein required for neurotr

130 ease from platelets, we examined the role of vesicle-associated membrane protein, SNAP-23, and syntax

131 These results show that vesicle-associated membrane protein, SNAP-23, and syntax

132 A vesicle-associated membrane protein, SNAP-23, and syntax

133 me-associated protein of 25 kD (SNAP25), and vesicle-associated membrane protein/synaptobrevin are co

134 Vesicle-associated membrane protein/synaptobrevin, a SNA

135 ransmission by cleaving the synaptic protein vesicle-associated membrane protein/synaptobrevin.

136 y oriented plasma membrane protein and VAMP (vesicle-associated membrane protein; synaptobrevin) is a

137 n three different PC12 cell lines expressing vesicle-associated membrane protein-T Antigen derivative

138 regulated, in part, by the interaction of a vesicle-associated membrane protein termed synaptobrevin

139 Synaptotagmin I is a synaptic vesicle associated membrane protein that appears to regu

140 totagmin 1 and 2 (syt 1, syt 2) are synaptic vesicle-associated membrane proteins that act as calcium

141 Deletion of synaptobrevin/vesicle-associated membrane protein, the major synaptic

142 e of FM1-43, or abolish immunoreactivity for vesicle-associated membrane protein, the toxin substrate

143 tein receptor tetanus neurotoxin insensitive vesicle-associated membrane protein (TI-VAMP)/VAMP7 was

144 rol fusion of tetanus neurotoxin insensitive vesicle-associated membrane protein (TiVAMP)/VAMP-7 vesi

145 Western blotting for vesicle-associated membrane protein type v-SNARE protein

146 yers bound soluble green fluorescent protein/vesicle-associated membrane protein (v-SNARE), and the S

147 asma membrane require the interaction of the vesicle-associated membrane protein VAMP with the plasma

148 xperiments using antibodies to synaptobrevin/vesicle associated membrane protein (VAMP) 1, 2, or rat

149 nsically disordered protein (IDP) regions of vesicle associated membrane protein (VAMP) driving a dis

150 fusion protein attachment receptor (v-SNARE) Vesicle associated membrane protein (VAMP), but a more s

151 of the SNARE complex, SNAP-25, Syntaxin, and vesicle associated membrane protein (VAMP/also Synaptobr

152 Vesicle associated membrane protein (VAMP; also known as

153 The juxtamembrane domain of vesicle-associated membrane protein (VAMP) 2 (also known

154 Recently, we identified vesicle-associated membrane protein (VAMP) 2 and 3 to be

155 ngly, complexin 2 was found to interact with vesicle-associated membrane protein (VAMP) 2, syntaxins

156 from the Golgi and reduced colocalization of vesicle-associated membrane protein (VAMP) 3-positive TN

157 romiscuous Qb,c-SNARE SNAP33 and the R-SNARE vesicle-associated membrane protein (VAMP) 721,722, also

158 The presence of vesicle-associated membrane protein (VAMP) and binary sy

159 ent protein receptor (SNARE) proteins of the vesicle-associated membrane protein (VAMP) and syntaxin

160 This protein forms a ternary complex with vesicle-associated membrane protein (VAMP) and syntaxin,

161 5 kDa (SNAP25) and the vesicle SNARE protein vesicle-associated membrane protein (VAMP) are essential

162 SNAP-25, syntaxin 1A, and synaptobrevin/vesicle-associated membrane protein (VAMP) are SNARE pro

163 pression of a syntaxin 4 mutant in which the vesicle-associated membrane protein (VAMP) binding site

164 Syntaxins and vesicle-associated membrane protein (VAMP) families, als

165 The vesicle-associated membrane protein (VAMP) family is ess

166 ctionally identify the site of action of the vesicle-associated membrane protein (VAMP) family of R-S

167 VAMP4, a recently discovered member of the vesicle-associated membrane protein (VAMP) family of tra

168 SNARE complexes between five proteins of the vesicle-associated membrane protein (VAMP) family, three

169 ferent members of the syntaxin, SNAP-25, and vesicle-associated membrane protein (VAMP) gene families

170 red a second pathway that sorts the synaptic vesicle-associated membrane protein (VAMP) into similarl

171 Synaptobrevin (Syb)/vesicle-associated membrane protein (VAMP) is a small, i

172 ertion sequence of the v-SNARE synaptobrevin/vesicle-associated membrane protein (VAMP) phenocopied t

173 at hippocampal synapses, using synaptobrevin/vesicle-associated membrane protein (VAMP) tagged with v

174 Synaptobrevin is a vesicle-associated membrane protein (VAMP) that is belie

175 We synthesized peptides based on vesicle-associated membrane protein (VAMP) to investigat

176 Our novel knock-in reporter lines of vesicle-associated membrane protein (vamp) zebrafish hom

177 Syntaxin, vesicle-associated membrane protein (VAMP), and synaptos

178 es comprised of the SNARE proteins syntaxin, vesicle-associated membrane protein (VAMP), and the syna

179 tion was inhibited by antibodies directed at vesicle-associated membrane protein (VAMP), demonstratin

180 The expression and localization of vesicle-associated membrane protein (VAMP), synaptic ves

181 1A, N-ethylmaleimide-sensitive factor (NSF), vesicle-associated membrane protein (VAMP), synaptosome-

182 Homologues of vesicle-associated membrane protein (VAMP), syntaxin, an

183 ein receptor (SNARE) proteins syntaxin 4 and vesicle-associated membrane protein (VAMP)-2 were also o

184 Vesicle-associated membrane protein (VAMP)-7 is found on

185 actin cytoskeleton and track the movement of vesicle-associated membrane protein (VAMP)-8-containing

186 ecular tracking of a model organelle tether, Vesicle-associated membrane protein (VAMP)-associated pr

187 The Vesicle-associated membrane protein (VAMP)-Associated Pr

188 N3, may depend on their interaction with the vesicle-associated membrane protein (VAMP)-associated pr

189 endoplasmic reticulum (ER)-resident proteins vesicle-associated membrane protein (VAMP)-associated pr

190 y colocalization at the plasma membrane with vesicle-associated membrane protein (VAMP).

191 SNARE and SNARE-associated proteins such as vesicle-associated membrane protein (VAMP)/synaptobrevin

192 synaptosome-associated protein (SNAP25), and vesicle-associated membrane protein (VAMP)/synaptobrevin

193 e used pharmacologic inhibitors of Snap25 or vesicle-associated membrane protein (VAMP)/synaptobrevin

194 The vesicle SNARE vesicle-associated membrane protein (VAMP)2 was also pre

195 Syntaxin 4 activation and docking/fusion of vesicle-associated membrane protein (VAMP)2-containing i

196 In both cell types, TNF colocalized with vesicle-associated membrane protein (VAMP)3-positive com

197 ral SNARE proteins were found in adipocytes: vesicle-associated membrane protein (VAMP-2), its relate

198 s of synaptophysin as well as synaptobrevin [vesicle-associated membrane protein (VAMP-2)], a protein

199 Similar to BoNT/B/D/F/G, BoNT/X cleaves vesicle-associated membrane proteins (VAMP) 1, 2 and 3,

200 nules in pancreatic acinar cells express two vesicle-associated membrane proteins (VAMP), VAMP2 and -

201 synaptosomal-associated protein 25 [SNAP25], vesicle-associated membrane protein [VAMP]) forming the

202 target SNARE syntaxin and the vesicle SNARE vesicle-associated membrane protein(VAMP).

203 actions involving components of the vesicle (vesicle-associated membrane protein; VAMP) and plasma me

204 oter to express SynaptopHluorin (pHluorin on vesicle-associated membrane protein (VAMP2)) or CalipHlu

205 d that the v-SNARE tetanus toxin-insensitive vesicle-associated membrane protein (VAMP7) differs from

206 of a fusogenic trans-SNARE complex involving vesicle-associated membrane protein (VAMP8), but not VAM

207 ensus on t-SNAREs usage, it is unclear which Vesicle Associated Membrane Protein (VAMPs: synaptobrevi

208 e show that two highly homologous exocytotic vesicle-associated membrane proteins (VAMPs) are require

209 s question, we evaluated the localization of vesicle-associated membrane proteins (VAMPs) in spread p

210 the role of vesicular SNARE proteins, i.e., vesicle-associated membrane proteins (VAMPs), remains en

211 teins from the vesicle membrane (R-SNAREs or vesicle-associated membrane proteins [VAMPs]) and the ta

212 f 25-kDa synaptosome-associated protein, and vesicle-associated membrane protein] were found to be ex

213 We show that VAMPs (vesicle-associated membrane proteins), which target vesi

214 Vesicle-associated membrane protein, which colocalizes w

215 Cleavage of vesicle-associated membrane protein with BoNtD or SNAP-2