ライフサイエンスコーパス: phospholipid bilayer

1 ural models of iPLA(2) in association with a 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 ing domains with their PI ligands and with a phospholipid bilayer.

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

11 ecular dynamics simulations of the CYPs in a phospholipid bilayer.

12 kB to recognize diacylglycerol embedded in a phospholipid bilayer.

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

14 a membrane-active peptide inserted within a phospholipid bilayer.

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

16 bstrate for deposition of a planar supported phospholipid bilayer.

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

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

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

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

21 confined within the hydrocarbon core of the phospholipid bilayer.

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

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

24 rtion of integral membrane proteins into the phospholipid bilayer.

25 lasma membrane and after reconstitution into phospholipid bilayer.

26 veals similarities in thickness to a typical phospholipid bilayer.

27 ations of transport across electropores in a phospholipid bilayer.

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

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

30 elices of apolipoprotein AI circumscribing a phospholipid bilayer.

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

32 effects on the structural properties of the phospholipid bilayer.

33 olving significant structural changes in the phospholipid bilayer.

34 etained following reconstitution into planar phospholipid bilayers.

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

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

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

38 led protein in unoriented liquid crystalline phospholipid bilayers.

39 found to selectively transport anions across phospholipid bilayers.

40 netically unfavorable fusion of the membrane-phospholipid bilayers.

41 se functional groups required for binding to phospholipid bilayers.

42 ied the beta3 cytoplasmic domain tethered to phospholipid bilayers.

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

44 milar to other biological interfaces such as phospholipid bilayers.

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

46 malism for molecular dynamics simulations of phospholipid bilayers.

47 alpha-synuclein binds to negatively charged phospholipid bilayers.

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

49 estabilizing and inducing transient pores in phospholipid bilayers.

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

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

52 are characterized in detergent micelles and phospholipid bilayers.

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

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

55 eractions between peptide antimicrobials and phospholipid bilayers.

56 is shown to translocate cooperatively across phospholipid bilayers.

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

58 exhibits voltage-gating properties in planar phospholipid bilayers.

59 cture and are oriented identically in planar phospholipid bilayers.

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

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

62 sion via direct interactions with Ca(2+) and phospholipid bilayers.

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

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

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

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

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

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

69 hermodynamics of this folding interaction in phospholipid bilayers.

70 meric cylinder that forms single channels in phospholipid bilayers.

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

72 ic molecules that can otherwise pass through phospholipid bilayers.

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

74 ed and characterized when reconstituted into phospholipid bilayers.

75 the latter after channel reconstitution into phospholipid bilayers.

76 ations affect the stability and structure of phospholipid bilayers?

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

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

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

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

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

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

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

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

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

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

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

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

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

90 , we probed if cross-dismutation operates in phospholipid bilayers and cell culture.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

107 14-3-3gamma, free in solution and bound to a phospholipid bilayer, and of the unphosphorylated peptid

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

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

110 Hybrid-supported phospholipid bilayers are a model structure utilized for

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

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

113 Although phospholipid bilayers are ubiquitous in modern cells, th

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

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

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

117 In pure phospholipid bilayers association occurs by contacts for

118 investigate the conformation of BM2(1-51) in phospholipid bilayers at high pH, which corresponds to t

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

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

121 f many embedded membrane proteins depends on phospholipid bilayer biophysical properties.

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

123 to investigate molecular orientations in the phospholipid bilayer but cannot resolve the actual distr

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

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

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

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

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

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

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

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

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

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

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

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

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

137 Single-membrane specimens, composed of a phospholipid bilayer containing a vectorially oriented v

138 By employing this method, phospholipid bilayers containing various concentrations

139 beta-arrestin with both the receptor and the phospholipid bilayer contribute to its functional versat

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

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

142 ity strongly depends on temperature and, for phospholipid bilayers, displays a maximum at the transit

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

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

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

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

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

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

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

150 eproducing catalysts capable of perpetuating phospholipid bilayer formation.

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

152 This study demonstrates the role of phospholipid bilayer fragment as the key intermediate in

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

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

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

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

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

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

159 via changes in biophysical properties of the phospholipid bilayer have received little study.

160 Freestanding phospholipid bilayers have been assembled spanning shall

161 Phospholipid bilayers have been intensively studied by m

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

163 nization of cell membranes and reconstituted phospholipid bilayers; however, the mechanisms by which

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

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

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

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

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

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

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

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

172 onstitutive activity observed in an isolated phospholipid bilayer indicates that beta(2)AR basal acti

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

174 In phospholipid bilayers, infrared dichroism data indicate

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

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

177 ansmembrane (TM) segments are moved from the phospholipid bilayer into cytosol, often together with h

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

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

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

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

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

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

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

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

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

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

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

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

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

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

192 phingolipids (GSLs), embedded in a supported phospholipid bilayer, is investigated by following the c

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

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

195 rent voltage-gated K(+) channels in hydrated phospholipid bilayer membrane environments.

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

197 nse of a voltage-gated K(+) channel within a phospholipid bilayer membrane to applied transmembrane v

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

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

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

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

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

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

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

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

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

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

208 Phospholipid bilayer Nanodiscs are a novel model membran

209 Phospholipid bilayer Nanodiscs are novel model membranes

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

211 Phospholipid bilayer nanodiscs have recently been shown

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

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

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

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

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

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

218 In the phospholipid bilayer of the endoplasmic reticulum the C

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

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

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

222 To elucidate the influence of the phospholipid bilayer on GPCR activation, here we interro

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

224 est that the interaction with the surface of phospholipid bilayers, operating as a change in bulk sol

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

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

227 The phospholipid bilayer plays a central role in the lifecyc

228 Phospholipid bilayer (PLB) coatings are very promising f

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

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

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

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

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

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

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

236 ation of membrane-embedded components within phospholipid bilayers represents a distinct class of pha

237 arbohydrate metabolism, modifications of the phospholipid bilayer, resistance to toxic compounds and

238 stic, molecular dynamics (MD) simulations of phospholipid bilayers responding to electric fields.

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

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

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

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

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

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

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

246 1-40) aggregation intermediates on supported phospholipid bilayers (SPBs) assembled at the crystal su

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

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

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

250 clofenac in the structural properties of the phospholipid bilayer, suggesting that both ionized and n

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

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

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

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

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

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

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

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

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

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

261 SAA solubilized phospholipid bilayers to form lipoproteins that provided

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

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

264 del for the axon that includes the APMS, the phospholipid bilayer, transmembrane proteins (TMPs), and

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

266 s can be utilized in anion transport through phospholipid bilayers under aqueous conditions for which

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

290 Phospholipid bilayers were studied by means of atomic fo

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

292 led receptor-G-protein complex embedded in a phospholipid bilayer, which serves as a benchmark to val

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

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

295 ptides to mediate the formation of supported phospholipid bilayers with two different types of membra

296 nt unilamellar vesicles (GUVs) consisting of phospholipids bilayers with different compositions.

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

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

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