ライフサイエンスコーパス: phospholipid bilayer

1 rtion of integral membrane proteins into the phospholipid bilayer.

2 s viral transmembrane proteins anchored in a phospholipid bilayer.

3 text of a native transmembrane protein and a phospholipid bilayer.

4 ely 100 A in diameter and the thickness of a phospholipid bilayer.

5 ructures taken from a simulation of GM1 in a phospholipid bilayer.

6 d approximates the chemical environment of a phospholipid bilayer.

7 ergy of the solid surface which supports the phospholipid bilayer.

8 e interactions between a solid surface and a phospholipid bilayer.

9 actions with isolated fatty acids and at the phospholipid bilayer.

10 ing domains with their PI ligands and with a phospholipid bilayer.

11 e mosaic than fluid, with little unperturbed phospholipid bilayer.

12 kB to recognize diacylglycerol embedded in a phospholipid bilayer.

13 solubilized via self-assembly in a nanoscale phospholipid bilayer.

14 ter molecules in the middle of the discoidal phospholipid bilayer.

15 bstrate for deposition of a planar supported phospholipid bilayer.

16 packing densities in the two leaflets of the phospholipid bilayer.

17 llography of 2D protein crystals in a native phospholipid bilayer.

18 microsomal delta12-desaturase (CREP-1) in a phospholipid bilayer.

19 ween the polar and hydrophobic layers of the phospholipid bilayer.

20 confined within the hydrocarbon core of the phospholipid bilayer.

21 dimer both in detergent solution and in the phospholipid bilayer.

22 erpendicular to the fatty acyl chains of the phospholipid bilayer.

23 elices of apolipoprotein AI circumscribing a phospholipid bilayer.

24 iour of OmpA in a detergent micelle and in a phospholipid bilayer.

25 liposomes by spontaneous insertion into the phospholipid bilayer.

26 ilayer and cholesterol levels present in the phospholipid bilayer.

27 m that mirrors the amphipathic nature of the phospholipid bilayer.

28 ral distributions (i.e., superlattices) in a phospholipid bilayer.

29 r weight of the AQP0 channel inserted in the phospholipid bilayer.

30 protruding from the hydrophobic core of the phospholipid bilayer.

31 a membrane-anchored protein into a supported phospholipid bilayer.

32 d carboxyl termini in the crystal and in the phospholipid bilayer.

33 dditionally increases ion leakage across the phospholipid bilayer.

34 lasma membrane and after reconstitution into phospholipid bilayer.

35 for the transport of potassium ions across a phospholipid bilayer.

36 veals similarities in thickness to a typical phospholipid bilayer.

37 olving significant structural changes in the phospholipid bilayer.

38 ural models of iPLA(2) in association with a phospholipid bilayer.

39 ations of transport across electropores in a phospholipid bilayer.

40 serted via a ring of membrane anchors into a phospholipid bilayer.

41 o its affinity toward the acyl chains in the phospholipid bilayers.

42 netically unfavorable fusion of the membrane-phospholipid bilayers.

43 se functional groups required for binding to phospholipid bilayers.

44 ied the beta3 cytoplasmic domain tethered to phospholipid bilayers.

45 two amantadine-binding sites exist in M2 in phospholipid bilayers.

46 milar to other biological interfaces such as phospholipid bilayers.

47 ti-alpha(IIb), which is known to dimerize in phospholipid bilayers.

48 malism for molecular dynamics simulations of phospholipid bilayers.

49 alpha-synuclein binds to negatively charged phospholipid bilayers.

50 the transmembrane domain of AM2 (AM2-TM) in phospholipid bilayers.

51 estabilizing and inducing transient pores in phospholipid bilayers.

52 able to form calcium channels in pure planar phospholipid bilayers.

53 e formation of aPL IgG-beta2GPI complexes on phospholipid bilayers.

54 are characterized in detergent micelles and phospholipid bilayers.

55 d by 10 ns molecular dynamics simulations in phospholipid bilayers.

56 oyl-2-oleoyl-sn-glycerophosphocholine (POPC) phospholipid bilayers.

57 eractions between peptide antimicrobials and phospholipid bilayers.

58 is shown to translocate cooperatively across phospholipid bilayers.

59 and retained pore-forming activity in planar phospholipid bilayers.

60 exhibits voltage-gating properties in planar phospholipid bilayers.

61 cture and are oriented identically in planar phospholipid bilayers.

62 on of this toxin with membranes using planar phospholipid bilayers.

63 ons, has a well-defined, stable structure in phospholipid bilayers.

64 bundle in vivo and in various detergents and phospholipid bilayers.

65 e Ca(2+)-dependent binding to the surface of phospholipid bilayers.

66 ly used liquid crystal-forming molecules and phospholipid bilayers.

67 y important fatty acid-activated function in phospholipid bilayers.

68 ed and characterized when reconstituted into phospholipid bilayers.

69 icelles; here, we extend this methodology to phospholipid bilayers.

70 fect on gramicidin A (gA) channels in planar phospholipid bilayers.

71 on the crystal structure of the protein over phospholipid bilayers.

72 hermodynamics of this folding interaction in phospholipid bilayers.

73 ng in the interfacial region of zwitterionic phospholipid bilayers.

74 f the lower partitioning of tolbutamide into phospholipid bilayers.

75 the latter after channel reconstitution into phospholipid bilayers.

76 etained following reconstitution into planar phospholipid bilayers.

77 nment (e.g., micelles) vs liquid crystalline phospholipid bilayers.

78 ed to further refine the domain structure in phospholipid bilayers.

79 mical potential and is applied to a stack of phospholipid bilayers.

80 led protein in unoriented liquid crystalline phospholipid bilayers.

81 ations affect the stability and structure of phospholipid bilayers?

82 study of AmB head-to-head dimerization in a phospholipid bilayer, a possible early stage of aggregat

83 y of proteins is Ca(2+)-dependent binding to phospholipid bilayers, a property that resides in the co

84 vior of photoresponsive foldamers bound in a phospholipid bilayer akin to a biological membrane phase

85 parison with a previous simulation of a pure phospholipid bilayer allows an atomic-level description

86 ied from Newcastle disease virus adsorb on a phospholipid bilayer and condense into fluidlike domains

87 d the affiliation of GLP-1 with a supported, phospholipid bilayer and determined its binding equilibr

88 tential because they cross the mitochondrial phospholipid bilayer and eliminate ROS at the heart of t

89 nge, occurs by passive diffusion through the phospholipid bilayer and passage through membrane protei

90 ormation concerning the location of 1 in the phospholipid bilayer and the conformations it can adopt

91 ocyte membrane that explicitly describes the phospholipid bilayer and the cytoskeleton, by extending

92 detectable decrease in affinity between the phospholipid bilayer and the solid surface as a result o

93 lts from the coupled dynamic response of the phospholipid bilayer and the spectrin molecular network.

94 nd PGPC on the structure of a multicomponent phospholipid bilayer and to assess the consequences of t

95 ores open by measuring ionic currents across phospholipid bilayers and cell membranes through the por

96 st as milliseconds, across both protein-free phospholipid bilayers and cell membranes.

97 s the formation of aPL-beta2GPI complexes to phospholipid bilayers and cells.

98 ely helical character when incorporated into phospholipid bilayers and detergent micelles.

99 MacA stimulated MacB ATPase only in phospholipid bilayers and did not need the presence of m

100 tructural characterization of self-assembled phospholipid bilayers and establish a framework for the

101 ave measured the adsorption of proteins onto phospholipid bilayers and found a strong correlation bet

102 this activity, but is able to associate with phospholipid bilayers and is potentially involved in mai

103 o immobilize IL-8 along with the receptor in phospholipid bilayers and is specific enough to result i

104 he membrane interactions of the peptide with phospholipid bilayers and its membrane topology using st

105 volved in the insertion of apoLp-III in both phospholipid bilayers and monolayers.

106 ated by a favorable surface interaction with phospholipid bilayers and set by lipid composition.

107 yl-2-oleoyl-sn-glycero-phosphocholine (POPC) phospholipid bilayers and studied utilizing solid-state

108 t FYVE domains bind PI(3)P in the context of phospholipid bilayers and that hydrophobic residues on a

109 to investigate the interactions of IAPP with phospholipid bilayers and the morphological effects of m

110 mic interplay between FERM domain binding to phospholipid bilayers and to its binding sites in the be

111 surface positively charged residues to bind phospholipid bilayers and trigger conformational changes

112 exas Red DHPE, which is doped into supported phospholipid bilayers and used as a pH-sensitive dye.

113 14-3-3gamma, free in solution and bound to a phospholipid bilayer, and of the unphosphorylated peptid

114 hydrated palmitoyloleoyl-phosphatidylcholine phospholipid bilayer, and simulated for 24 ns in total.

115 stable isotopes, reconstituted into oriented phospholipid bilayers, and their detailed topology deter

116 d on solid-state NMR experiments in oriented phospholipid bilayers; and one based on two-dimensional

117 These results suggest that supported fluid phospholipid bilayers are not homogenous at the nanoscal

118 Uniaxially aligned phospholipid bilayers are often used as model membranes

119 ed by gramicidin A (GA) dimers inserted into phospholipid bilayers are reported as a function of the

120 Although phospholipid bilayers are ubiquitous in modern cells, th

121 ynthetic peptides incorporated into oriented phospholipid bilayer arrays, consistent with the idea th

122 hydration dynamics gradient found across the phospholipid bilayer as an intrinsic ruler for determini

123 Most C(2)-domains bind to phospholipid bilayers as a function of Ca(2+).

124 QP0 reconstituted with random orientation in phospholipid bilayers as single particles.

125 radient, induce ionic currents across planar phospholipid bilayers, as well as in cultured osteosarco

126 In pure phospholipid bilayers association occurs by contacts for

127 charged nanoparticles onto single-component phospholipid bilayers bearing phosphocholine headgroups

128 e protein inserted into magnetically aligned phospholipid bilayers (bicelles) using EPR spectroscopy.

129 in A5 (A5) forms 2-dimensional crystals over phospholipid bilayers, blocking their availability for c

130 d by the convex surface associating with the phospholipid bilayer by a calcium bridging mechanism.

131 d in a 1,2-dimyristoyl-3-phosphatidylcholine phospholipid bilayer by molecular dynamics simulations.

132 scidin 1 was studied in magnetically aligned phospholipid bilayers by oriented-sample solid-state NMR

133 ion of the hydration water at the surface of phospholipid bilayers by use of coherent anti-Stokes Ram

134 Additionally, 3D nanoprobes modified with phospholipid bilayers can enter single cells to allow ro

135 olecules into fluid liquid-disordered (L(d)) phospholipid bilayers can produce liquid-ordered (L(o))

136 or diffusion of neutral molecules across the phospholipid bilayer, can provide the isolation and prec

137 bind more efficiently to negatively charged phospholipid bilayer cellular surfaces, and will more re

138 co-glycolic acid), cholesteryl oleate, and a phospholipid bilayer coat that is decorated with triphen

139 aline phosphatase was linked to biotinylated phospholipid bilayers coated inside poly(dimethylsiloxan

140 CTB binding was monitored on supported phospholipid bilayers coated on the walls and floors of

141 gated the specific molecular interactions of phospholipid bilayers composed of 1-[(2)H(31)]palmitoyl-

142 We investigated how local changes in phospholipid bilayer composition modulate the activity o

143 ynamics simulations of the UraA symporter in phospholipid bilayers consisting of: 1) 1-palmitoyl 2-ol

144 fluid phase transition behavior in supported phospholipid bilayers constructed from 1,2-dimyristoyl-s

145 By employing this method, phospholipid bilayers containing various concentrations

146 nst solvated dimyristoyl phosphatidylcholine phospholipid bilayer disintegration on contact with the

147 NMR spectrum of Pf1 coat protein in aligned phospholipid bilayers displayed better resolution than t

148 polytopic membrane proteins in their native phospholipid bilayer environment under physiological con

149 re sensitive to and altered by the peptide's phospholipid bilayer environment, which exerts a dynamic

150 NMR spectroscopy in two magnetically-aligned phospholipid bilayer environments (bicelles) that differ

151 nces in macroscale biophysical properties of phospholipid bilayers even within a single, contiguous p

152 membrane, underscoring the importance of the phospholipid bilayer for physiological activity.

153 using mild detergents and reconstituted into phospholipid bilayers for biochemical studies.

154 ed and reconstituted in liposomes and planar phospholipid bilayers, form constitutively open anion ch

155 eproducing catalysts capable of perpetuating phospholipid bilayer formation.

156 functions of the most abundant mitochondrial phospholipids, bilayer-forming phosphatidylcholine (PC)

157 r fusion mechanisms converge at a pathway of phospholipid bilayer fusion.

158 , sphingosine has been found to permeabilize phospholipid bilayers, giving rise to vesicle leakage.

159 on of an antimicrobial peptide, MSI-78, with phospholipid bilayers has been investigated using atomic

160 id that can form lipid microdomains in fluid phospholipid bilayers has been shown to be enzymatically

161 erties of these nanopores when embedded in a phospholipid bilayer have been explored by molecular dyn

162 imulations of the isolated SecY protein in a phospholipid bilayer have been performed to explore the

163 Freestanding phospholipid bilayers have been assembled spanning shall

164 Phospholipid bilayers have been intensively studied by m

165 .e., uncomplexed, or complexed to albumin or phospholipid bilayers); however, (iii) transfer kinetics

166 coefficient similar to that of protein-free phospholipid bilayers; (ii) oleic acid rapidly crosses t

167 and as purified protein reconstituted into a phospholipid bilayer in the form of high density lipopro

168 e peptides did not significantly disrupt the phospholipid bilayer in the L(alpha) phase.

169 state of the protein and inserts across the phospholipid bilayer in the membrane-bound state.

170 sis of the interactions between PMCA and the phospholipid bilayer in which it is embedded show that i

171 access a hidden conformational state on the phospholipid bilayer in which only the higher-affinity m

172 o be capable of translocating protons across phospholipid bilayers in proteoliposome systems.

173 fuse (flip-flop) rapidly across protein-free phospholipid bilayers in their un-ionized form.

174 The binding of LtxA to phospholipid bilayers increased by 4 orders of magnitude

175 ptide incorporated into magnetically aligned phospholipid bilayers indicated that the peptide is tilt

176 three examples: spontaneous adhesion between phospholipid bilayers induced by low pH, polymer-induced

177 In phospholipid bilayers, infrared dichroism data indicate

178 tack bacterial membranes and upon landing on phospholipid bilayers instantaneously (seconds) convert

179 ate molecules results in the conservation of phospholipid bilayer integrity.

180 ve an intrinsic ability to remodel vesicular phospholipid bilayers into discrete protein-lipid comple

181 ily proteins are touted to girdle eukaryotic phospholipid bilayers into narrow tubules for traffickin

182 t a convenient construct to mimic the native phospholipid bilayer, investigate the effects of membran

183 proteins in their native environment of the phospholipid bilayer is critical for understanding physi

184 interface formed between the protein and the phospholipid bilayer is inaccessible to high-resolution

185 glucagon-like peptide-1 (GLP-1) to a planar phospholipid bilayer is measured using single-molecule t

186 king experiments on a planar solid-supported phospholipid bilayer is presented that establishes condi

187 e alpha-hemolysin (alphaHL) pore in a planar phospholipid bilayer is sandwiched between two layers of

188 The aggregation of AmB molecules in a phospholipid bilayer is, thus, crucial for the drug's ac

189 Micellar phase transitions of phospholipid bilayers is a well-known but little-studied

190 lithographic route for micropatterning fluid phospholipid bilayers is demonstrated in which spatially

191 s during the de novo synthesis of biomimetic phospholipid bilayers is described.

192 er, the behavior of the designed peptides in phospholipid bilayers is essentially identical to their

193 show that retardation of water motions near phospholipid bilayers is extended by the presence of a m

194 th cell-attached membrane patches and planar phospholipid bilayers is not observed in corresponding m

195 The energy of intermediates in fusion of phospholipid bilayers is sensitive to kappa(m), the sadd

196 nto nanodiscs, which are soluble disk-shaped phospholipid bilayers, is an ideal solution to these pro

197 natural amino acid side chains from water to phospholipid bilayers make a major contribution to the a

198 py specimen protocol shows that the presumed phospholipid bilayer membrane ribbons that wind helicall

199 coupling of a porphyrin dimer embedded in a phospholipid bilayer membrane.

200 orbed onto or incorporated into the cationic phospholipid bilayer membrane.

201 due to their effect in the decomposition of phospholipid bilayer membrane.

202 bacterial outer membrane protein, NanC, in a phospholipid bilayer membrane.

203 reports the distribution coefficient between phospholipid bilayer membranes and phosphate buffered sa

204 ow provide evidence that sulfonylureas cross phospholipid bilayer membranes rapidly and effectively b

205 ng domains can be translocated across planar phospholipid bilayer membranes.

206 ure and dynamics of the Vpu(1-40) monomer in phospholipid bilayer membranes.

207 It also forms a channel in planar phospholipid bilayer membranes.

208 nthetic PB1-F2 (sPB1-F2) peptide with planar phospholipid bilayer membranes.

209 crown ethers as entry portals and that span phospholipid bilayer membranes.

210 e diffusion of sulfonylurea compounds across phospholipid bilayer membranes.

211 In the presence of a phospholipid bilayer, MinD bound to the bilayer and recr

212 Phospholipid bilayer Nanodiscs are a novel model membran

213 Phospholipid bilayer Nanodiscs are novel model membranes

214 In the present work, we explore phospholipid bilayer nanodiscs as membrane mimics and em

215 Phospholipid bilayer nanodiscs have recently been shown

216 itations by reconstituting unlabeled LeuT in phospholipid bilayer nanodiscs, subjecting them to hydro

217 icon photonic microring resonator arrays and phospholipid bilayer nanodiscs, which together allow mul

218 eins in vivo and of in vitro self-assembling phospholipid bilayer nanodiscs.

219 ution of a bacterial biotin transporter into phospholipid bilayer nanodiscs.

220 e (UMP) molecules confined in multi-lamellar phospholipid bilayers, nanoscopic films, ammonium chlori

221 Raman scattering from the phospholipid bilayer of a single, trapped liposome could

222 In the phospholipid bilayer of the endoplasmic reticulum the C

223 ciated peptidoglycan and to the (31)P of the phospholipid bilayer of the membrane.

224 Here, supported phospholipid bilayers of DMPC (1,2-dimyristoyl-sn-glycer

225 ns of dodecyl maltoside (DM), digitonin, and phospholipid bilayers of two compositions.

226 re, we present evidence for the influence of phospholipid bilayers on complex formation between rabbi

227 econstituted high-density lipoprotein (rHDL) phospholipid bilayer particle together with the stimulat

228 s and the structural parameters required for phospholipid bilayer partitioning are elucidated.

229 onary surfactant protein B (SP-B(1-25)) in a phospholipid bilayer (PB) was determined by fluorescence

230 The phospholipid bilayer plays a central role in the lifecyc

231 Phospholipid bilayer (PLB) coatings are very promising f

232 anticoagulant protein that crystallizes over phospholipid bilayers (PLBs), blocking their availabilit

233 domain of PLB (24-52) was incorporated into phospholipid bilayers prepared from 1-palmitoyl-2-oleoyl

234 The protein was incorporated into phospholipid bilayers prepared from a mixture of 1,2-dio

235 its ability to oligomerize and interact with phospholipid bilayers, processes closely linked to the b

236 lipophilicity, allowing tmTCEP to penetrate phospholipid bilayers rapidly (>30-fold faster than DTT)

237 ns at atomic resolution with solution NMR in phospholipid bilayers, rather than in detergent micelles

238 or studying the thermodynamics of folding in phospholipid bilayers remains a considerable challenge.

239 ral distribution of molecules in cholesterol/phospholipid bilayers remains elusive.

240 ts of macroscopically oriented S4 peptide in phospholipid bilayers revealed a tilt angle of 40 degree

241 ew method for producing mechanically aligned phospholipid bilayer samples using naphthalene, a sublim

242 cs simulations on CEACAM1-S in an asymmetric phospholipid bilayer show migration of Ca(2+) ions to th

243 asurements of prothrombinase activity on the phospholipid bilayers showed that the aPL mAbs reduced t

244 nt VDAC-1 can form voltage-gated channels in phospholipid bilayers similar to those of the native pro

245 d has been designed for patterning supported phospholipid bilayers (SLBs) on planar substrates and in

246 Sub-100 nm wide supported phospholipid bilayers (SLBs) were patterned on a planar

247 Supported phospholipid bilayers (SPBs) are valuable models for fun

248 1-40) aggregation intermediates on supported phospholipid bilayers (SPBs) assembled at the crystal su

249 d fusion of lipid vesicles to form supported phospholipid bilayers (SPBs) on surfaces.

250 t membranes where they assist in maintaining phospholipid bilayer stability.

251 x couples that are physically separated by a phospholipid bilayer, such as iron uptake and redox sign

252 achieve properties similar to pure saturated phospholipid bilayers, suggesting that complete lateral

253 l evidence that water molecules close to the phospholipid bilayer surface are ordered with the symmet

254 nt HDL are discoidal complexes composed of a phospholipid bilayer surrounded by protein alpha-helices

255 rong inhibition of translocation in a planar phospholipid bilayer system.

256 s and kinetics of a di-mannose molecule in a phospholipid bilayer system.

257 e peptide also integrated readily into mixed phospholipid bilayers that resemble Gram-positive membra

258 r-infrared (NIR) dye IR780 into the liposome phospholipid bilayer, the bilayer would be disrupted by

259 and MtrC exposed on the outer surface of the phospholipid bilayer, the established in vivo orientatio

260 In a phospholipid bilayer, the positively charged L-selectin

261 labeled at Cys382 and reconstituted into the phospholipid bilayers, the spin label partitions activel

262 alpha-helical structure and to interact with phospholipid bilayers through amphipathic alpha-helices.

263 of a 1-palmitoyl,2-oleoylphosphatidylcholine phospholipid bilayer to be 52 +/- 2 cm/s, close to the p

264 ne KALP peptides (sequence: GKK(LA)nLKKA) in phospholipid bilayers to investigate hydrophobic mismatc

265 locate in the polar headgroup region of the phospholipid bilayer, to induce bilayer thinning, and to

266 within the hydrophobic core of the discoidal phospholipid bilayer transforming it into a spherical HD

267 is when colloidal beads diffuse along linear phospholipid bilayer tubes whose radius is the same as t

268 Solid-state (2)H NMR spectroscopy of phospholipid bilayers under osmotic stress allows struct

269 porter MerF determined in liquid crystalline phospholipid bilayers under physiological conditions by

270 -length and truncated constructs of CXCR1 in phospholipid bilayers under physiological conditions.

271 ice by incorporating native RyR1 into planar phospholipid bilayers under voltage-clamp conditions.

272 nd cyclooxygenase-2 (COX-2), interact with a phospholipid bilayer using molecular dynamics simulation

273 ipase A(2) catalyzed hydrolysis of supported phospholipid bilayers using neutron reflection and ellip

274 otein of Pf1 bacteriophage was determined in phospholipid bilayers using orientation restraints deriv

275 holesterol-binding site of the M2 protein in phospholipid bilayers using solid-state NMR spectroscopy

276 olved in micelles, bicelles, or occasionally phospholipid bilayers using X-ray diffraction or magneti

277 ons of the complete talin head domain with a phospholipid bilayer, using multiscale molecular dynamic

278 he motional and organizational properties of phospholipid bilayers, using several NMR methods, demons

279 -dioleoyl-sn-glycero-3-phosphocholine (DOPC) phospholipid bilayer via multi-nanosecond molecular dyna

280 based cortical cytoskeleton connected to the phospholipid bilayer via multiple protein bridges.

281 el nonsteroidal anti-inflammatory drug, in a phospholipid bilayer was examined in molecular detail by

282 netics on the lateral membrane pressure in a phospholipid bilayer was investigated by sum-frequency v

283 ecular dynamics model of rhodopsin in a POPC phospholipid bilayer was simulated for 15 ns, revealing

284 mbrane, the recombinant SNARE complex in the phospholipid bilayer was studied using fluorescence quen

285 trum of (15)N-labeled Leu39 PLB in DOPC/DOPE phospholipid bilayers was 220 ppm and is characteristic

286 el phase transition temperature of supported phospholipid bilayers was tested in the presence of suga

287 enzyme in its natural environment, which is phospholipid bilayers, we developed a method that allows

288 ticle-tracking microrheology to freestanding phospholipid bilayers, we find that the membranes are no

289 to the cytochrome bc1 complex embedded in a phospholipid bilayer were measured by plasmon waveguide

290 d-lipid interactions across cholesterol-rich phospholipid bilayers were investigated by measuring nea

291 Phospholipid bilayers were studied by means of atomic fo

292 NMR studies on deuterated POPC (sn-1 chain) phospholipid bilayers when the PLB peptide was inserted

293 sis), but not area expansion modulus, Ka, of phospholipid bilayers, whereas monomeric X31 peptide low

294 from the beta-sheet interface to contact the phospholipid bilayer with basic and hydrophobic residues

295 ulations to analyze AQP4 in cholesterol-free phospholipid bilayers with similar elastic properties bu

296 ro- or nano-particles enveloped by PEGylated phospholipid bilayers, with protein antigens covalently

297 tolbutamide, were found to incorporate into phospholipid bilayers, with the ionizable sulfonamide ex

298 eptides directly through the plasma membrane phospholipid bilayer without involving chirally specific

299 a(2+), reconstituted OmpLA diffused within a phospholipid bilayer without revealing any signs of phos

300 The receptor is in liquid crystalline phospholipid bilayers, without modification of its amino