ライフサイエンスコーパス: bilayer membrane

1 incorporated into the cationic phospholipid bilayer membrane.

2 ) in a dipalmitoylphosphatidylcholine (DPPC) bilayer membrane.

3 both structures embedded in a solvated lipid bilayer membrane.

4 the concentration of cations near the lipid bilayer membrane.

5 ties to affect the dynamics of a surrounding bilayer membrane.

6 e in the electrode-supported thiolipid/lipid bilayer membrane.

7 release channel incorporated into the lipid bilayer membrane.

8 yl group of LY329332 did not insert into the bilayer membrane.

9 of gingival recession with a novel collagen bilayer membrane.

10 holipids located in the inner leaflet of the bilayer membrane.

11 l destabilization and leakiness of the lipid bilayer membrane.

12 occupied by an exchangeable molecule in the bilayer membrane.

13 group, enabling it to interact with a lipid bilayer membrane.

14 ugh a 2.6-nm diameter ion channel in a lipid bilayer membrane.

15 heir different localization within the lipid bilayer membrane.

16 , with a size range of 40-150 nm and a lipid bilayer membrane.

17 n capture surface based on a supported lipid bilayer membrane.

18 effect in the decomposition of phospholipid bilayer membrane.

19 phosphatases in an integrated in vitro lipid bilayer membrane.

20 er membrane protein, NanC, in a phospholipid bilayer membrane.

21 en it is added to only one side of the lipid bilayer membrane.

22 ing the magnitude of the peptide tilt in the bilayer membrane.

23 ing hydrophobicity as well a supported lipid bilayer membrane.

24 a porphyrin dimer embedded in a phospholipid bilayer membrane.

25 stallization, as well as reconstitution into bilayer membranes.

26 as transverse diffusion of phospholipids in bilayer membranes.

27 nd 1,2-dilauroyl-sn-glycero-3-phosphocholine bilayer membranes.

28 e adopt a moderate average tilt within lipid bilayer membranes.

29 ic acid, using blot overlay assays and model bilayer membranes.

30 nizing physical dynamics of biological lipid-bilayer membranes.

31 fied receptors inserted into deposited lipid bilayer membranes.

32 domain wall fluctuations of phase-separated bilayer membranes.

33 n be translocated across planar phospholipid bilayer membranes.

34 tudy the mechanical properties of soft lipid bilayer membranes.

35 ics of the Vpu(1-40) monomer in phospholipid bilayer membranes.

36 action between the peptide and the POPG/POPC bilayer membranes.

37 were uniformly distributed within artificial bilayer membranes.

38 croscopy, and detergent extractions in model bilayer membranes.

39 also forms a channel in planar phospholipid bilayer membranes.

40 eptide, penetratin, to solid-supported lipid bilayer membranes.

41 2 (sPB1-F2) peptide with planar phospholipid bilayer membranes.

42 as entry portals and that span phospholipid bilayer membranes.

43 probes for structural and dynamic studies of bilayer membranes.

44 f sulfonylurea compounds across phospholipid bilayer membranes.

45 to have high pore-forming activity in planar bilayer membranes.

46 rrel-stave model for pore formation in lipid bilayer membranes.

47 al ion coordination self-organize into lipid bilayer membranes.

48 sional concentration of SOPC in unilamellar, bilayer membranes.

49 in secondary structure and topology in lipid bilayer membranes.

50 mpF channels reconstituted into planar lipid bilayer membranes.

51 ibraries for members that permeabilize lipid bilayer membranes.

52 gulated traffic through normally impermeable bilayer membranes.

53 nnel protein reconstituted into phospholipid bilayer membranes.

54 frozen-hydrated 2D crystals of AQP1 in lipid bilayer membranes.

55 n by tPMP-1 by using artificial planar lipid bilayer membranes.

56 agglutinin (HA) of influenza virus to planar bilayer membranes.

57 ce lateral reorganization of lipids in fluid bilayer membranes.

58 posed His, Lys, and Arg side chains in lipid bilayer membranes.

59 membranes and incorporated into planar lipid bilayer membranes.

60 ollow the kinetics of halide flux across the bilayer membranes.

61 d directly to lipid acyl chains within lipid bilayer membranes.

62 forms ion-permeable channels in planar lipid bilayer membranes.

63 steps for transport of FA across pure lipid bilayer membranes.

64 FTR) chloride channel reconstituted in lipid bilayer membranes.

65 on-permeable channels in planar phospholipid bilayer membranes.

66 vesicles for reconstitution studies in lipid bilayer membranes.

67 main formation in partially suspended single bilayer membranes.

68 Cl(-) ion binding and transport across lipid bilayer membranes.

69 DOPC)and dilauroylphosphatidylcholine (DLPC) bilayer membranes.

70 exes, coat protomers, that bud vesicles from bilayer membranes.

71 ole in the regulation of protein function by bilayer membranes.

72 ed as ideal to transport anions across lipid bilayer membranes.

73 gulfs the forespore, surrounding it with two bilayer membranes.

74 ceramides are known to interact favorably in bilayer membranes.

75 ctionally reconstituted into synthetic lipid bilayer membranes.

76 and separated from the environment by lipid bilayer membranes.

77 tely 32 mN/m that is suggested to prevail in bilayer membranes.

78 he process by which cyclotides interact with bilayer membranes.

79 re stages of phase separation in model lipid bilayer membranes.

80 les that span 5 degrees -35 degrees in lipid bilayer membranes.

81 e molecular dynamics simulations in explicit bilayer membranes.

82 tetrabutylamide 2 (1) forms ion channels in bilayer membranes, (2) mediates ion transport across cel

83 y dissolved h-IAPP to voltage-clamped planar bilayer membranes (a cell-free in vitro system) also cau

84 The dipole potential of a lipid bilayer membrane accounts for its much larger permeabili

85 etic signal transducer embedded in the lipid bilayer membrane acts as a switchable catalyst, catalyzi

86 re from the cis to the trans side of a lipid bilayer membrane, allowed to refold and interact with th

87 ansverse and lateral structures of the lipid bilayer membrane, along with a description of lipid and

88 these cross-beta assemblies, both across the bilayer membrane and along the nanotube length, provides

89 upported planar egg phosphatidylcholine (PC) bilayer membrane and complex formation with plastocyanin

90 ized magnetic crystals surrounded by a lipid bilayer membrane and organized into chains via a dedicat

91 rted in a palmitoyloleoylphosphatidylcholine bilayer membrane and solvated by simple point charge wat

92 er and a dipalmitoylphospatidylcholine lipid bilayer membrane and to the free energies of solute tran

93 of ethyl phosphorothioate groups insert into bilayer membranes and kill cancer cells.

94 We used supported bilayer membranes and nanometer-scale structures fabrica

95 istribution coefficient between phospholipid bilayer membranes and phosphate buffered saline (PBS) me

96 structure and regulated deformation of lipid bilayer membranes are among a cell's most fascinating fe

97 Bilayer membranes are characterized by large lateral str

98 membrane as the support structure for lipid bilayer membranes are presented.

99 Artificial lipid-bilayer membranes are valuable tools for the study of me

100 icles, containing baskets of type 1 in their bilayer membrane, are unique assemblies and important fo

101 ed detection is demonstrated with a tethered bilayer membrane array built in parallel microchannels.

102 Thus, with the planar bilayer membranes as target, hemifusion can precede pore

103 bilize TnI by covalent amine coupling, while bilayer membrane-associated protein, nAChR, was noncoval

104 bly of free block copolymer molecules into a bilayer membrane at the complex surface.

105 hospholipid (dimyristoylphosphatidylcholine) bilayer membranes at 308 K are studied, many of them for

106 -1) amphiphiles of various tail lengths into bilayer membranes at different pH values, we show that t

107 ) were fused to voltage-clamped planar lipid bilayer membranes at low pH.

108 r absence of an envelope composed of a lipid-bilayer membrane, attributes that profoundly affect stab

109 ical that experiments investigating rafts in bilayer membranes avoid the production of peroxides.

110 uced probe rotational rates occurring within bilayer membranes below the phospholipid phase transitio

111 Normal and diseased cells release bilayered membrane-bound nanovesicles into interstitial

112 then embed this Cu catalyst inside a hybrid bilayer membrane by depositing a monolayer of lipid on t

113 the specific conductance of artificial lipid bilayer membranes by the formation of ion-permeable chan

114 nt to the plane of a confined patch of fluid bilayer membrane can create lateral concentration gradie

115 ength comparable to the thickness of a lipid bilayer membrane can self-insert into the membrane.

116 Supported lipid bilayer membranes can be assembled and patterned on thes

117 -association and enhanced affinity for lipid bilayer membranes, compared to the wild-type peptide.

118 e collagen fibers combined with a resorbable bilayer membrane composed of non-cross-linked porcine ty

119 of cholesterol and alpha-tocopherol on lipid bilayer membranes composed of different phosphatidylchol

120 Lipid bilayer membranes composed of DOPC, DPPC, and a series o

121 Many of the properties of bilayer membranes composed of simple single-chain amphip

122 forces governing the adhesion between mixed bilayer membranes comprising lactosyl ceramide (LacCer)

123 nally reconstituted membrane proteins into a bilayer membrane confirmed predictions made by these FP-

124 o proton translocation across a closed lipid bilayer membrane, conserving the free energy released by

125 ular dynamics computer simulation of a lipid bilayer membrane consisting of cholesterol and 1-stearoy

126 ptide, penetratin, and solid-supported lipid bilayer membranes consisting of either egg phosphatidylc

127 ed phases utilizing a theoretical model of a bilayer membrane containing cholesterol, dipalmitoyl pho

128 mics, and free energy simulations in a mixed bilayer membrane containing dipalmitoylphosphatidylcholi

129 cular dynamics simulations of hydrated lipid bilayer membranes containing highly polyunsaturated fatt

130 o investigate the structure and hydration of bilayer membranes containing S1-S4 voltage-sensing domai

131 rystals can undergo directed nucleation from bilayer membranes containing two-dimensional (2D) choles

132 ion of single alpha-hemolysin pores into the bilayer membrane, demonstrating the possibility of using

133 Multicomponent lipid bilayer membranes display rich phase transition and asso

134 Line tension at fluid lipid bilayer membrane domain boundaries controls the kinetics

135 per part (n < 8) of the curvature frustrated bilayer membranes (DOPE) may be significantly relaxed on

136 Upon reconstitution into the lipid bilayer membrane, Drosophila RyR-C formed a large conduc

137 These peptides are stabilised in a lipid bilayer membrane environment and they are preferentially

138 to decipher or assign directly in the lipid-bilayer membrane environment.

139 or samples of 1) oriented diI in model lipid bilayer membranes, erythrocytes, and macrophages; and 2)

140 to pyranine, its impermeability to the lipid bilayer membrane, fast kinetics of binding, and ability

141 mphiphilic block copolymers into a supported bilayer membrane for defined coating of nanoparticles.

142 constants of CPR/CYP2C9 complexes in a lipid bilayer membrane for the first time.

143 molecular mechanisms by which heme traverses bilayer membranes for use in biosynthetic reactions are

144 mycin E, when incorporated into planar lipid bilayer membranes, forms two types of channels (small an

145 Lipid bilayer membranes found in nature are heterogeneous mixt

146 econstituted into an artificial planar lipid bilayer membrane from the point of view of electric sign

147 heet aggregates upon partitioning into lipid bilayer membranes from the aqueous phase where the pepti

148 the delta exon5 CFTR proteins into the lipid bilayer membrane, functional phosphorylation- and ATP-de

149 ermediates and transition states involved in bilayer membrane fusion.

150 involved in the standard stalk mechanism of bilayer membrane fusion.

151 to the membrane normal of DOPC or DPPC lipid bilayer membranes, GWALP23-R14 shows one major state who

152 haracterizing thermodynamic phases of single bilayer membranes has not been possible due to their ext

153 ure transmembrane-protein diffusion in lipid bilayer membranes have advanced in recent decades, provi

154 channels in an ion-conducting state in lipid bilayer membranes have so far been unsuccessful.

155 ly, model membrane systems, such as tethered bilayer membranes, have been developed for surface-depen

156 In this report, we use a hybrid bilayer membrane (HBM) as an electrochemical platform to

157 ton flux using an electrode-supported hybrid bilayer membrane (HBM).

158 e, T(m), of the distal lipid layer in hybrid bilayer membranes (HBMs) under water was investigated us

159 formation of phospholipid/alkanethiol hybrid bilayer membranes (HBMs).

160 hypothesis postulates the existence of lipid bilayer membrane heterogeneities, or domains, supposed t

161 highly anisotropic environment of the lipid bilayer membrane imposes significant constraints on the

162 We have characterized the resulting hybrid bilayer membrane in air using atomic force microscopy, s

163 ization of a phospholipid/alkanethiol hybrid bilayer membrane in air.

164 include explicit H(2)O and an infinite lipid bilayer membrane in molecular dynamics (MD) simulations

165 as interacts with a negatively charged lipid bilayer membrane in multiple orientations.

166 Stabilization of the lipid bilayer membrane in red blood cells by its association w

167 method for simulating a two-component lipid bilayer membrane in the mesoscopic regime is presented.

168 inated SPR gold chip established a supported bilayer membrane in which cell receptor monosialoganglio

169 also reflect the energetic landscape of the bilayer membrane in which synthetic ion channels functio

170 id (PL)/free (unesterified) cholesterol (FC) bilayer membranes in cell and cell-free systems are comp

171 roducible method to form free-standing lipid bilayer membranes in microdevices made with Norland Opti

172 proteins transduce information across lipid bilayer membranes in response to extra-cellular binding

173 s into, and at least partially across, lipid bilayer membranes in the absence of any auxiliary protei

174 re changes in intramembrane potential of the bilayer membranes in two different preparations, lipid v

175 ive amyloid fibrils, permeabilized synthetic bilayer membranes in vitro.

176 e skeleton attachment to the fluidlike lipid bilayer membrane, including a specific accounting for th

177 um microelectrodes are modified with a lipid bilayer membrane incorporating cholesterol oxidase.

178 noscale structural reorganization of a lipid bilayer membrane induced by a chemical recognition event

179 show that in both DOPC- and DMoPC-containing bilayers, membrane-inserted residues all along the A cha

180 an exclusive property of the peptide in the bilayer membrane interface.

181 ysine, tryptophan, and even glycine at lipid bilayer membrane interfaces.

182 Peptides with this motif assembled on bilayer membranes into beta-sheets and formed transient

183 The lipid bilayer membrane is 4.6 nm thick, with a low-electron-de

184 bulk solubility diffusion model in which the bilayer membrane is represented as a slab of bulk hexade

185 nanoscale dynamic organization within lipid bilayer membranes is central to our understanding of cel

186 plification of chemical signals across lipid bilayer membranes is of profound significance in many bi

187 nstituted into dimyristoylphosphatidycholine bilayer membranes is predominantly alpha-helical and has

188 and acceptor molecules in two apposing lipid bilayer membranes is used to resolve topographical featu

189 interactions with a rigid more ordered lipid bilayer membrane, is regulated in plasma membranes by ch

190 that peptide 1a interacts with anionic lipid bilayer membranes, like oligomers of full-length alpha-s

191 ped virus particles (those that lack a lipid-bilayer membrane) must breach the membrane of a target h

192 tryptophan indole ring, with respect to the bilayer membrane normal, and of a principal order parame

193 Because of the bilayer membrane of liposomes, which can accommodate ten

194 on and to cholesterol contained in the lipid bilayer membrane of vesicles.

195 es and moderate to high dynamic averaging in bilayer membranes of 1,2-dioleoylphosphatidylcholine, 1,

196 spin-labeled lipid chains in fully hydrated bilayer membranes of dimyristoyl phosphatidylcholine con

197 ivity was low when compared with activity on bilayer membranes of mixed PS and phosphatidylcholine (P

198 e determined in oriented phosphatidylcholine bilayer membranes of varying thickness using solid-state

199 physical insight into the influence of lipid bilayer membranes on conformer preferences and conformer

200 s of sterols and sphingolipids in the target bilayer membranes on properties of fusion pores.

201 bellflower model demonstrate that in a lipid bilayer membrane or a detergent micelle, the cytoplasmic

202 ructure in solution in the absence of either bilayer membranes or detergents at physiological tempera

203 a2+-ATPase involves PLN monomers, in a lipid bilayer membrane, PLN monomers form stable pentamers of

204 Physical penetration of lipid bilayer membranes presents an alternative pathway for ce

205 idence that sulfonylureas cross phospholipid bilayer membranes rapidly and effectively by a free-diff

206 sport of free fatty acids (FFA) across lipid bilayer membranes remains a subject of debate.

207 the most potent anion transporters in lipid bilayer membranes reported to date.

208 itoring protein-induced charge flux across a bilayer membrane represents a universal method for quant

209 ated from these transfected cells into lipid bilayer membrane resulted in single Ca(2+) release chann

210 pleted protein preparation incorporated into bilayer membranes resulted in a similar increase in the

211 rotocol shows that the presumed phospholipid bilayer membrane ribbons that wind helically to form the

212 assay for cholera toxin (CT) using supported bilayer membranes (SBMs) in a poly(dimethylsiloxane) (PD

213 urfaces as a platform to construct supported bilayer membranes (SBMs) is demonstrated, and improved p

214 nsitive technique were performed on a hybrid bilayer membrane (self-assembled monolayer of thiahexa (

215 tructures determined experimentally in lipid bilayer membranes show that eefxPot affords significant

216 ct between the electrode and a vesicle lipid bilayer membrane shows a response that correlates with v

217 r dynamics simulation with an explicit lipid bilayer membrane, similar to the system used for the sol

218 labeled cages on spherically supported lipid bilayer membranes (SSLBM) formed on silica beads, and th

219 sin are therefore the effect of the toxin on bilayer membrane structure and the nature of the self-as

220 zation of the effect that pneumolysin has on bilayer membrane structure resulting from oligomerizatio

221 on within synthetic cells comprising a lipid bilayer membrane surrounding an aqueous polymer solution

222 To construct this hybrid bilayer membrane system, we prepare an example of a synt

223 microscropically unresolvable rafts in lipid bilayers, membrane tension led to the appearance of larg

224 rmation of rafts was studied by using planar bilayer membranes that contained rhodamine-phosphatidyle

225 oration of PSI trimeric complexes into DPhPG bilayer membranes that mimic the natural thylakoid membr

226 Integral membrane proteins reside within the bilayer membranes that surround cells and organelles, pl

227 counterparts, which are surrounded by lipid bilayer membranes, these microbial organelles are bounde

228 Many proteins are anchored to lipid bilayer membranes through a combination of hydrophobic a

229 cytochrome c and to destabilize planar lipid bilayer membranes through reduction of pore line tension

230 The surfactant permeabilizes the lipid bilayer membrane to facilitate release of an encapsulate

231 slocate from one monolayer of a phospholipid bilayer membrane to the other in a concentration and vol

232 olecular transducer from one side of a lipid bilayer membrane to the other.

233 ammalian cells is the adherence of the lipid bilayer membrane to the underlying membrane associated c

234 reticulum, lowers the rigidity of the lipid bilayer membrane to which it binds.

235 The self-assembly of lipid bilayer membranes to enclose functional biomolecules, th

236 enza virus were fused to planar phospholipid bilayer membranes to evaluate the effects of sterols and

237 Finally, we show that peptides can cross bilayer membranes to localize encapsulated RNA.

238 on techniques to form myelin-mimicking lipid bilayer membranes to measure both the association and di

239 rticles bind selectively to the open edge of bilayer membranes to stabilize otherwise transient amphi

240 ological channels in supported and suspended bilayer membranes, to considering completely abiotic des

241 In planar bilayer membranes, trypsin-nicked PA makes cation-select

242 r absence of an envelope - an external lipid bilayer membrane typically carrying one or more viral gl

243 Lipid bilayer membranes--ubiquitous in biological systems and

244 ive (MS) channel gated by tension in a lipid bilayer membrane under stresses due to fluid flows.

245 The behavior of freestanding lipid bilayer membranes under the influence of dielectric forc

246 Studies of bilayer membranes using steady-state probe-partitioning

247 ecause they are simple amphiphiles that form bilayer membrane vesicles that retain encapsulated oligo

248 The existence of a bilayer membrane was corroborated in giant vesicles thro

249 eptide cecropin A (CecA) in the phospholipid bilayer membrane was determined using (15)N solid-state

250 kyl phosphate in the lipid layer of a hybrid bilayer membrane, we regulate proton transport to a Cu-b

251 groups within the hydrocarbon core of lipid bilayer membranes, we examined the structural and functi

252 ocations within dioleoyl-phosphatidylcholine bilayer membranes, we measure pK(a) values below 7.0.

253 mechanism and channel formation in the lipid bilayer membranes were confirmed for the most active mol

254 Highly stable and fluid supported bilayer membranes were fabricated by fusion of positivel

255 is known to be supplied by both their lipid bilayer membranes, which resist bending and local change

256 e to produce a protoplast, surrounded by two bilayer membranes, which separate it from the cytoplasm

257 [nido-7-CH3(CH2)15-7,8-C2B9H11] (MAC) in the bilayer membrane while encapsulating the hydrophilic spe

258 matically increases the conductance of lipid bilayer membranes, while non-cytotoxic rat amylin does n

259 polyvalent lipid PI(4,5)P2 in the plane of a bilayer membrane with high affinity.

260 olecules within the inner leaflet of a lipid bilayer membrane with possible binding sites on Kir chan

261 reveals the transport of water across lipid bilayer membranes with a relative water permeability as

262 been established definitively, especially in bilayer membranes with physiologically relevant lipid co

263 spectroscopy using POPC and POPG/POPC (3/1) bilayer membranes with sn-1 chain perdeuterated POPC and

264 elective channels across acidic phospholipid bilayer membranes with spontaneous transitions over a wi

265 They are surrounded by a classical bilayered membrane with an exceptionally high cholestero

266 taneously translocate across synthetic lipid bilayer membranes without permeabilization.