ライフサイエンスコーパス: biological membrane

1 rting electrons across an energy-transducing biological membrane.

2 the conformation of the APP-TM domain at the biological membrane.

3 brane domains, for transporter embedded in a biological membrane.

4 mediate the transfer of fatty acids across a biological membrane.

5 t reduces quinone and pumps protons across a biological membrane.

6 l species via a series of acceptors across a biological membrane.

7 ve the ability to rapidly internalize across biological membranes.

8 the translocation of small molecules across biological membranes.

9 nd hydrolysis to facilitate transport across biological membranes.

10 l the mechanism of attack translates to real biological membranes.

11 hat can quantify antibiotic transport across biological membranes.

12 as a general feature of the organization of biological membranes.

13 rely on dedicated transport systems to cross biological membranes.

14 a passive structural role as the backbone of biological membranes.

15 h catalyze the transport of phospholipids in biological membranes.

16 id nanoparticles (liposomes) as a mimicry of biological membranes.

17 the bilayer normal that naturally occurs in biological membranes.

18 cific roles of lipid structure remodeling in biological membranes.

19 o control the transport of Cl(-) ions across biological membranes.

20 ons cause the softening or stiffening of the biological membranes.

21 pted 'universal' value (~1 microF/cm(2)) for biological membranes.

22 erve to transport a variety of anions across biological membranes.

23 ically coupled exchange of Cl- and H+ across biological membranes.

24 on the formation of oligomeric pores within biological membranes.

25 itectures, the most prominent examples being biological membranes.

26 on encountered for proteins diffusing within biological membranes.

27 olding steps or secretion across one or more biological membranes.

28 etic COSAN membranes and naturally occurring biological membranes.

29 tant principle for the spatial patterning of biological membranes.

30 However, in vivo, Rab11 recruits RCP onto biological membranes.

31 ments, especially oxidizing environments and biological membranes.

32 lateral heterogeneities in lipid systems and biological membranes.

33 is particularly appropriate for the study of biological membranes.

34 highly conserved and essential components of biological membranes.

35 eins undergo random and passive diffusion in biological membranes.

36 ers use ATP to drive solute transport across biological membranes.

37 ing the transport of monocarboxylates across biological membranes.

38 ilms and the role of lateral organization in biological membranes.

39 ame material determines the interaction with biological membranes.

40 t of water and small neutral solutes through biological membranes.

41 ls that translocate monovalent anions across biological membranes.

42 holipids can confer a net negative charge on biological membranes.

43 e to the heterogeneous and dynamic nature of biological membranes.

44 stems that translocate cargo into and across biological membranes.

45 ane pores when in contact with detergents or biological membranes.

46 e of observed interactions between Abeta and biological membranes.

47 ys a significant role in shaping and curving biological membranes.

48 ated ion channels are excitable nanopores in biological membranes.

49 els that facilitate the flow of water across biological membranes.

50 rolling the dynamic structural properties of biological membranes.

51 phospholipids are an important component of biological membranes.

52 ng the organization and physical behavior of biological membranes.

53 upon interaction with other proteins and/or biological membranes.

54 e these proteins to fuse two closely apposed biological membranes.

55 imulations cannot yet span the complexity of biological membranes.

56 d-protein interactions play pivotal roles in biological membranes.

57 inding of Cu between the dissolved phase and biological membranes.

58 protons that allow for fast diffusion along biological membranes.

59 investigating supramolecular interactions in biological membranes.

60 tting analysis of EX-TM-CYTO interactions in biological membranes.

61 the structural and functional properties of biological membranes.

62 d in concert with various proteins, RNA, and biological membranes.

63 mposition in the inner and outer leaflets of biological membranes.

64 mer's disease, potentially via disruption of biological membranes.

65 bilize cholesterol-dependent nanoclusters in biological membranes.

66 udy the nanoscale dynamics of cholesterol in biological membranes.

67 kinetics at a water/oil interface in lieu of biological membranes.

68 he selective translocation of solutes across biological membranes.

69 stic estimates of the yield areal strains of biological membranes.

70 ly leading to substrate translocation across biological membranes.

71 omoting receptor self-association within the biological membranes.

72 Phospholipids are major constituents of biological membranes.

73 because most proteins fail to traffic across biological membranes.

74 to those observed for anomalous diffusion in biological membranes.

75 turally occurring domains, such as rafts, in biological membranes.

76 rom soluble proteins by their insertion into biological membranes.

77 couple mechanosensitive elements in crowded biological membranes.

78 ndamental building blocks of glycans in many biological membranes.

79 noparticle assemblies, and interactions with biological membranes.

80 s from static quenching FRET measurements in biological membranes.

81 ions against concentration gradients across biological membranes.

82 of FE tell us about the overall structure of biological membranes?

83 eins and the overall mechanical stability of biological membranes?

84 S6 intercalates biological membranes acting as a hydrophobic support for

85 nal involvement of membrane micro-domains in biological membranes, alphaS-induced domain formation ma

86 Fusion of biological membranes, although mediated by divergent pro

87 anostructure, which is able to cross several biological membranes and accumulate in tumor tissues by

88 ide (DDAB) was used to mimic lipid layers of biological membranes and acted as an interface between G

89 Polyunsaturated phospholipids are common in biological membranes and affect the lateral structure of

90 ve important roles as structural entities of biological membranes and as regulators of cellular growt

91 liposomes, are versatile tools for modelling biological membranes and delivering foreign objects to c

92 e toxic alpha-synuclein oligomers to perturb biological membranes and disrupt cellular function; thes

93 and synthetic amphiphiles serve as mimics of biological membranes and enable the delivery of drugs, p

94 nanodevices which controllably interact with biological membranes and even mimic the function of natu

95 d JGDs serve as powerful tools for mimicking biological membranes and for biomedical applications suc

96 es from proteins during translocation across biological membranes and hence play a vital role in cell

97 neutralization and energy transport through biological membranes and hydrogen fuel cells.

98 the importance of lipid species diversity in biological membranes and importantly, it suggests that m

99 ystem that mimics the mechanical behavior of biological membranes and is able to self-assemble into c

100 ade characterization of such organization in biological membranes and model systems difficult.

101 he nature of the interactions of alphaS with biological membranes and provide insights into their rol

102 ting their close proximity to the channel in biological membranes and supporting their functional rel

103 ayer-spanning, monovalent cation channels in biological membranes and synthetic bilayers.

104 The heterogeneity of lipid composition of biological membranes and the effect of lipid molecules o

105 of the lateral organization of components in biological membranes and the evolution of this arrangeme

106 ies alter subsequent interactions with model biological membranes and the Gram-negative bacterium She

107 underlying lateral heterogeneity (rafts) in biological membranes and the role of domains in the regu

108 and hybrid DSs, their similar thickness with biological membranes and their imaging by fluorescence a

109 ver, the widely observed differences between biological membranes and their in vitro counterparts are

110 e valuable models for fundamental studies of biological membranes and their interaction with biologic

111 ; however, TGs are not capable of traversing biological membranes and therefore need to be cleaved by

112 The thicknesses of biological membranes and vesicles self-assembled from am

113 uipped to carry therapeutic molecules across biological membranes and, therefore, have been widely re

114 stinal tract, steric constraints in crossing biological membranes, and clearing by enterohepatic circ

115 specificity, segregation between solvent and biological membranes, and interaction transience are dir

116 , triolein, of the type present in skin oil, biological membranes, and most cooking oils was oxidized

117 rmation and membrane organization in complex biological membranes, and provide a background for unrav

118 ul new means to study molecular movements in biological membranes, and the technology is widely appli

119 Biological membranes are a crucial aspect of living syst

120 A significant fraction of lipids in biological membranes are charged.

121 Biological membranes are complex, self-organized structu

122 Biological membranes are constantly exposed to forces.

123 Because biological membranes are diverse and nonuniform, we expl

124 Biological membranes are exposed to a number of chemical

125 Lipid bilayers and biological membranes are freely permeable to CO(2), and

126 Although biological membranes are involved in fibril plaque forma

127 Because interactions with biological membranes are key for Ras function, Ras-lipid

128 Mechanical properties of biological membranes are known to regulate membrane prot

129 tched surfaces provided strong evidence that biological membranes are organized as lipid bilayers wit

130 Biological membranes are organized into dynamic microdom

131 Unlike their model membrane counterparts, biological membranes are richly decorated with a heterog

132 Biological membranes are tricky to investigate.

133 Biological membranes are two dimensional, making the dis

134 understand the mechanism of transport in the biological membrane as a whole, the effects of the lipid

135 orated fluid films, such as bubble films and biological membranes, as well as fundamental implication

136 The curvature of biological membranes at the nanometer scale is criticall

137 l changes observed in synthetic and isolated biological membranes, BAs reorganized intact cell membra

138 ability to probe the viscoelastic effects of biological membranes, becoming a new tool for tribology

139 ponses, not only as structural components of biological membranes, but also as signalling mediators.

140 ticipate in C4-dicarboxylate movement across biological membranes, but only one of these utilizes an

141 tion, tension regulation, and trafficking in biological membranes, but the mechanisms responsible for

142 Imaging of biological membranes by environmentally sensitive solvat

143 enzymes that actively transport ions across biological membranes by interconverting between high (E1

144 imersomes (DSs), with similar thicknesses to biological membranes by simple injection from ethanol so

145 The diverse lipid environment of the biological membrane can modulate the structure and funct

146 The structure and composition of a biological membrane can severely influence the activity

147 nfirm that the global physical properties of biological membranes can act as information pathways bet

148 The structural organization of proteins in biological membranes can affect their function.

149 Model biological membranes can be employed for systematic inve

150 In this contribution we show that biological membranes can catalyze the formation of supra

151 Biological membranes can dramatically accelerate the agg

152 Biological membranes carry fixed charges at their surfac

153 In biological membranes, changes in lipid composition or me

154 nterest in developing synthetic analogues of biological membrane channels with high efficiency and ex

155 ry and many key transport characteristics of biological membrane channels.

156 pid bilayer, represent a simplified model of biological membrane channels.

157 folding and binding, molecular machines, and biological membrane channels.

158 he resulting biomimetic nanorobots possess a biological membrane coating consisting of diverse functi

159 Biological membranes composed of lipids and proteins are

160 Biological membranes contain ion channels, which are nan

161 SMA) is a polymer that extracts nanodiscs of biological membranes (containing membrane proteins) from

162 Interactions of macrolide antibiotics with biological membranes contribute to their bioavailability

163 We asked if a biological membrane could employ kinetic energy to trans

164 ructs in which the affinity of the toxin for biological membranes could be activated or deactivated b

165 Biological membranes create compartments, and are usuall

166 protein scaffolding is a key feature of many biological membranes, creating gradients in nanoparticle

167 Biological membranes define not only the cell boundaries

168 Biological membranes define the boundaries of cells and

169 have a differential effect on heterogeneous biological membranes, depending on their local compositi

170 model may be useful for understanding other biological membrane domains whose distributions display

171 bstitution, which precludes diffusion across biological membranes, e.g., blood-brain barrier.

172 rom synthetic membranes can be translated to biological membranes, enabling the formation of gel fibe

173 Curving biological membranes establishes the complex architectur

174 The transport of charged molecules across biological membranes faces the dual problem of accommoda

175 family, facilitate extraction of lipids from biological membranes for their loading onto CD1d molecul

176 These membranes have similar dimensions to biological membranes found in cells, and previously COSA

177 Fluidity is essential for many biological membrane functions.

178 Biological membrane fusion proceeds via an essential top

179 SNARE proteins catalyze many forms of biological membrane fusion, including Ca(2+)-triggered e

180 Its interaction with the lipid part of biological membranes has been the subject of intensive s

181 Active transport in biological membranes has been traditionally studied usin

182 n lipid components in raftlike structures of biological membranes, has not been fully explored.

183 membrane abnormalities to various diseases, biological membranes have been acknowledged as targets f

184 For example, design features from biological membranes have been applied to break the perm

185 tner or capable of mimicking the fluidity of biological membranes have been conceived by multitopic i

186 Biological membranes have layers of varying hydrophobici

187 blish and maintain phospholipid asymmetry in biological membranes; however, little is known about the

188 aired monoacylglycerol lipase recruitment to biological membranes in post-mortem Alzheimer's tissues,

189 r mechanisms of protein translocation across biological membranes in precisely defined experimental c

190 -binding proteins that transport ions across biological membranes in response to light.

191 maximum stability and dynamic properties to biological membranes in response to nutritional or envir

192 hese bright Arch variants enable labeling of biological membranes in the far-red/infrared and exhibit

193 Furthermore, RemCA directly binds to biological membranes in vitro, shows higher affinity for

194 nal region, which suggests interactions with biological membranes in vivo.

195 likely to create cell-like hybrids from any biological membrane including human cells and thus may e

196 id-lipid interactions can laterally organize biological membranes into domains of distinct structures

197 The nanoscale organization of biological membranes into structurally and compositional

198 erogeneous distribution of components in the biological membrane is critical in the process of cell p

199 es, translocation of the permeant across the biological membrane is traditionally assumed to obey the

200 ination of inorganic gold nanoparticles with biological membranes is a compelling way to develop biom

201 equired for transport (ESCRT) machinery from biological membranes is a critical final step in cellula

202 One key feature of nearly all biological membranes is a distinct lipid asymmetry.

203 Proton diffusion (PD) across biological membranes is a fundamental process in many bi

204 The transfer of fatty acids across biological membranes is a largely uncharacterized proces

205 Gated ion transport across biological membranes is an intrinsic process regulated b

206 Signal transduction across biological membranes is central to life.

207 The lipid bilayer typical of hydrated biological membranes is characterized by a liquid-crysta

208 The curvature of biological membranes is controlled by membrane-bound pro

209 hich lipids regulate protein function within biological membranes is critical for understanding the m

210 Translocation of proteins across biological membranes is essential for life.

211 proteins and the lipid-bilayer component of biological membranes is expected to mutually influence t

212 The scission of biological membranes is facilitated by a variety of prot

213 Permeability (P(m)) across biological membranes is of fundamental importance and a

214 Nitrate and nitrite transport across biological membranes is often facilitated by protein tra

215 on of light energy into ion gradients across biological membranes is one of the most fundamental reac

216 mbrane, revealing that the hydrophobicity of biological membranes is significantly higher than apprec

217 The fluid mosaic model of biological membranes is that of a two-dimensional lipid

218 The lateral organization of biological membranes is thought to take place on the nan

219 iven that the local concentration of PIP2 in biological membranes is variable, spontaneous curvature

220 Regulated ion diffusion across biological membranes is vital for cell function.

221 Proton diffusion along biological membranes is vitally important for cellular e

222 arnessing nanoscale mechanical energy within biological membranes, it is possible to promote controll

223 mining variable in confined systems, and, in biological membranes, it may provide a means to regulate

224 The fusion of sealed biological membranes joins their enclosed aqueous compar

225 Many S. aureus toxins damage biological membranes, leading to cell death.

226 in-induced lipid exchange is used to prepare biological membrane-like asymmetric small unilamellar ve

227 dynamics simulation data suggest that, in a biological membrane, lipid molecules occupy this peripla

228 scinating yet poorly studied molecules among biological membrane lipids.

229 In biological membranes, many factors such as cytoskeleton,

230 cal requirement for charge to balance across biological membranes means that the transmembrane transp

231 ties of dendrimersomes to serve as versatile biological membrane mimics.

232 that computer simulations genuinely research biological membranes, not just lipid bilayers.

233 reflect lipid-phase separation events in the biological membrane of the GJ plaque, leading to increas

234 Generation of chemical gradients across biological membranes of cellular compartments is a hallm

235 The biological membranes of many cell types contain large-po

236 approach toward more complex systems such as biological membranes or energy conversion devices, adapt

237 cused on nanoparticles that bind strongly to biological membranes or induce membrane damage, leading

238 rs bound in a phospholipid bilayer akin to a biological membrane phase.

239 These results contrast biological membrane physics and the physics of thin, rig

240 The elastic and viscous properties of biological membranes play a vital role in controlling ce

241 Biological membranes play an essential role in living or

242 Understanding the lateral organization of biological membranes plays a key role on the road to ful

243 Phase separation in biological membranes plays an important role in protein

244 Biological membranes present a highly fluid environment,

245 to both study and enhance the production of biological membrane proteins.

246 However, the mechanisms of transport across biological membranes remain unclear.

247 pore formation in planar lipid bilayers and biological membranes, resulting in an inability to intox

248 Biological membranes segregate into specialized function

249 e investigated in situ the ultrastructure of biological membranes, selected from several cell types f

250 s well as the understanding of mechanisms of biological membrane shaping.

251 nt electrostatic interactions, colloidal and biological membranes share many of the same physical sym

252 copolymers offer a detergent-free method for biological membrane solubilisation to produce SMA-lipid

253 in mammalian lipids have profound effects on biological membrane structure, dynamics and lipid second

254 The intricate shapes of biological membranes such as tubules and membrane stacks

255 s affect the composition and organization of biological membranes, suggesting a potential mechanism f

256 ers associated in distinct ways with various biological membranes, suggesting that a detailed investi

257 The biological membrane surrounding fat globules in milk (th

258 eir interaction strengths were measured in a biological membrane system.

259 terogeneous spatial-temporal organization of biological membrane systems.

260 nificant part of the functional processes in biological membranes takes place at the molecular level;

261 ovide a better model for the organization of biological membranes than lipid mixtures with microscale

262 tions between receptor EX-TM-CYTO domains in biological membranes that are important in regulation of

263 In biological membranes the alignment of embedded proteins

264 In systems mimicking biological membranes, the CD3 chain localization is modu

265 Given the abundance of unsaturated lipids in biological membranes, the continuous generation of hydro

266 e these are less than perfect mimics of true biological membranes, the structures are often confirmed

267 e membranes in fuel cells to ion channels in biological membranes, the well-specified control of ioni

268 of rhodopsin activation incurred by the non-biological membranes: the cationic membrane drives a tra

269 n channel proteins control ionic flux across biological membranes through conformational changes in t

270 he ability to efficiently translocate across biological membranes through still poorly-characterized

271 lasmic leaflet to the cytoplasmic leaflet of biological membranes, thus generating and maintaining tr

272 How a nonenveloped virus transports across a biological membrane to cause infection remains mysteriou

273 n CA activity suggests that the tightness of biological membranes to CO(2) may uniquely be regulated

274 d mechanism is that the peptides assemble in biological membranes to form beta-barrel shaped oligomer

275 in the specific transport of ammonia across biological membranes to mitigate ammonia toxicity and ai

276 ts an approach to exploit size and charge of biological membranes to overcome barriers for treatment

277 rstanding how alpha-synuclein interacts with biological membranes to promote neurological disease mig

278 Numerous bacterial toxins can cross biological membranes to reach the cytosol of mammalian c

279 study unveils a novel design concept of non-biological membranes to reconstitute and harness GPCR fu

280 Polar lipids must flip-flop rapidly across biological membranes to sustain cellular life [1, 2], bu

281 tors that couple proton translocation across biological membranes to the synthesis/hydrolysis of ATP.

282 receptor) proteins mediate fusion by pulling biological membranes together via a zippering mechanism.

283 Proton transfer across biological membranes underpins central processes in biol

284 s are pumps that transport substrates across biological membranes using the energy of ATP hydrolysis.

285 In biological membranes, various protein secretion devices

286 The fluid mosaic model for biological membranes was formulated 40 years ago.

287 ultiwalled carbon nanotubes (MWNTs) on model biological membranes was investigated using a quartz cry

288 interactions affected domain organization in biological membranes, we assayed the effects of BAs on b

289 To mimic charged biological membranes, we studied phase separation and do

290 passively modulating the local properties of biological membranes, when in contact with a support suc

291 Membrane proteins are embedded in the biological membrane where the chemically diverse lipid e

292 tegrates indiscriminately into virtually any biological membrane, where it forms sevenfold pyramids.

293 ion of the reactants can also be relevant in biological membranes, where Ch, polyunsaturated fatty ac

294 Sterols are crucial components of biological membranes, which are synthetized in the ER an

295 d monolayers of defined composition to mimic biological membranes, which were probed by x-ray reflect

296 de mimics of double-bilayer and multibilayer biological membranes with dimensions and number of bilay

297 dacy of glycodendrimersomes as new mimics of biological membranes with programmable glycan ligand pre

298 volves the interaction of these species with biological membranes, with a subsequent loss of integrit

299 ble to deliver its catalytic domain across a biological membrane without the need for any eukaryotic

300 adily soluble in aqueous buffer, yet crosses biological membranes without cellular assistance: an une