ライフサイエンスコーパス: membrane surface

1 o polyamide coated crystals (mimicking an RO membrane surface).

2 monomer-monomer interactions of CDCs at the membrane surface.

3 There was less accumulation of BSA on the membrane surface.

4 o organize their spatial distribution at the membrane surface.

5 nteractions between the bacteria and charged membrane surface.

6 n of the applied electrical potential to the membrane surface.

7 l interactions between the N-glycans and the membrane surface.

8 packed amphiphilic helices that rest on the membrane surface.

9 ne and increased the roughness factor of the membrane surface.

10 pendent on the anionic charge density of the membrane surface.

11 ter having found a stable orientation at the membrane surface.

12 nds to a specific region of LPS close to the membrane surface.

13 viscous "suction" at close proximity to the membrane surface.

14 iquid and DAMO organisms attach close to the membrane surface.

15 t interactions with the fluid and functional membrane surface.

16 ne headgroup is approximately 20 A above the membrane surface.

17 repeated after the Cu-NPs dissolve from the membrane surface.

18 te flux during bacterial accumulation on the membrane surface.

19 , and peripheral proteins are located at the membrane surface.

20 ction between the C domains of FVIII and the membrane surface.

21 e segment 2 (TM2) and TM3 on the cytoplasmic membrane surface.

22 GPR30 protein levels residing at the plasma membrane surface.

23 membrane and likely embed the helix into the membrane surface.

24 s within a transmembrane segment or near the membrane surface.

25 reduced amounts and was undetectable on the membrane surface.

26 transmembrane segment or at a site near the membrane surface.

27 re by means of complex interactions with the membrane surface.

28 t gases as well as CO2 reactant gases on the membrane surface.

29 of respiratory syncytial virus bound on the membrane surface.

30 ucleotides to anchor proteins to a supported membrane surface.

31 aturated lipids, are thought to organize the membrane surface.

32 orms an extended alpha-helix parallel to the membrane surface.

33 distribution of proteins and lipids over the membrane surface.

34 suitable for the modeling of iPLA(2) at the membrane surface.

35 f PLB's cationic cytoplasmic domain with the membrane surface.

36 coiled to helical structures when bound to a membrane surface.

37 ordered and does not interact with the model membrane surface.

38 asal activity, even mutants distant from the membrane surface.

39 ffinity synergistic interaction, even at the membrane surface.

40 up to 61 degrees C when piscidin 1 is on the membrane surface.

41 late to the two-dimensional environment of a membrane surface.

42 rated and surrounded by areas of hydrophobic membrane surface.

43 -helices of Hsp12 in SDS micelles lie on the membrane surface.

44 d composition of the associated phospholipid membrane surface.

45 to a model of how MinE persists at the MinD-membrane surface.

46 the N terminus anchors these proteins to the membrane surface.

47 in the reversible binding of annexin to the membrane surface.

48 has been challenging because it occurs on a membrane surface.

49 ance diffusion of the electron donors at the membrane surface.

50 how a disordered protein can interact with a membrane surface.

51 nates only at distances beyond 10 A from the membrane surface.

52 y fold up into alpha-helical segments on the membrane surface.

53 ecruit multiple active PI3K molecules to the membrane surface.

54 ctively optimizing substrate turnover at the membrane surface.

55 not have a similar tendency to adhere to the membrane surface.

56 ls and increase of the hydrophilicity of the membrane surface.

57 e a helix orientation of K * parallel to the membrane surface.

58 enhances leakage through fiber growth on the membrane surface.

59 e the non-specific binding of antigen on the membrane surface.

60 d open structure BSA layer was formed on the membrane surface.

61 ted by gentle rubbing of a PVC eraser on the membrane surface.

62 ad no effect on Cav2.2 protein levels on the membrane surface.

63 ticles uniformly distributed over the entire membrane surfaces.

64 s to and assembles clathrin on highly curved membrane surfaces.

65 ert protein or polymer, and by adsorption to membrane surfaces.

66 nd in similar probe volumes near protein and membrane surfaces.

67 y of encounter with target complexes on cell membrane surfaces.

68 ion is a general property of native H-Ras on membrane surfaces.

69 and by phycobilisomes situated on thylakoid membrane surfaces.

70 ed by the stiffness of the lateral and basal membrane surfaces.

71 nsity on the extracellular and intracellular membrane surfaces.

72 al different classes of protein which act on membrane surfaces.

73 d full-length Syt1 to interact with opposing membrane surfaces.

74 brane packing defects found on highly curved membrane surfaces.

75 rmembrane space and by the 2D environment of membrane surfaces.

76 rs but also localization and distribution in membrane surfaces.

77 m regular lattices on cylindrically deformed membrane surfaces.

78 aids promoted the adsorption of foulants on membrane surfaces.

79 e function of blood coagulation factor Xa on membrane surfaces.

80 profiles, and protrusions extended from all membrane surfaces.

81 r understanding many biological processes at membrane surfaces.

82 atures of multiprotein signaling pathways on membrane surfaces.

83 e O-H bands (compared with C-H bands) on the membrane surface after cycles 1 and 5.

84 ined relatively unchanged in FTIR-spectra of membrane surfaces after only one cycle.

85 of these extracellular molecules across the membrane surface allows rapid screening of the biofilm c

86 insertions is to anchor proteins strongly to membrane surfaces, amplifying steric pressure.

87 e develop, to our knowledge, a new method of membrane surface analysis.

88 ory T state that interacts strongly with the membrane surface and a less inhibitory R state that inte

89 in which the peptide lies almost flat on the membrane surface and alternates between kinked and strai

90 Endophilin lattices expose large areas of membrane surface and are held together by promiscuous in

91 the 3E6 epitope faces the negatively charged membrane surface and Arg2320 is poised at the center of

92 ed surface charge density from the increased membrane surface and associated glycoproteins.

93 associated proteins that laminates the inner membrane surface and attaches to the overlying lipid bil

94 determinants of insertion suggests that the membrane surface and dipole potentials are driving force

95 mately 75 residues that lies parallel to the membrane surface and has been proposed to play a mechani

96 on, which results in its accumulation at the membrane surface and hence in a potential response.

97 y to amphipaths, a helix that runs along the membrane surface and is connected to the pore via a glyc

98 Protein G was covalently linked on the membrane surface and it was successfully used for the or

99 lis (B. subtilis) by bacterial growth on the membrane surface and its exposure to bacterial suspensio

100 magainin 2, resists self-association at the membrane surface and penetrates further into the hydroph

101 in the peripheral elements close to the cell-membrane surface and produced Ca(2+) signals that propag

102 re may have sequestered mGluR5 away from the membrane surface and that the loss of surface mGluR5 inh

103 he attractive charge interaction between the membrane surface and the deprotonated Glu134 residue of

104 an open activation gate at the intracellular membrane surface and the intracellular C-terminal domain

105 SPR peak shift due to protein binding to the membrane surface and then characterized the lipid-bindin

106 ly, a small number of cyclotides bind to the membrane surface and then insert first into the outer me

107 s enable these proteins to polymerize on the membrane surface and undergo two-dimensional phase separ

108 meric [KIGAKI](3) swims around freely on the membrane surface and undergoes considerable motional ave

109 differences include adsorption on the lipid membrane surfaces and partitioning into the center of li

110 (XPS) were used to characterize foulants on membrane surfaces and rigorously deduce their contributi

111 beta-sheet FP is immobilized, resides on the membrane surface, and causes significant membrane curvat

112 al chain pressure, low charge density at the membrane surface, and increased salt concentration promo

113 ive and negative residues, net charge of the membrane surface, and low hydrophobicity of TM VII actin

114 in a higher deposition rate of BSA onto the membrane surface, and the formation of a denser BSA laye

115 orces, the adsorption behavior of BSA on the membrane surface, and the structure of the BSA adsorbed

116 tide PI(4,5)P2 attract the protein to acidic membrane surfaces, and myristoylation increases the affi

117 ar interactions between the foulants and the membrane surface are analyzed by direct force measuremen

118 opy demonstrated that cells deposited on the membrane surface are inactivated, resulting in a layer o

119 t lipid bilayer structures and low curvature membrane surface are preferable for CYP2B4-cytb5 complex

120 of common techniques for modification of the membrane surface are reviewed, including surface coating

121 manufacturing process, luminal and abluminal membrane surfaces are characterized by differences in ch

122 er fracturing, limited regions of the actual membrane surfaces are revealed.

123 al cells build apical microvilli to increase membrane surface area and enhance absorptive capacity.

124 ion was evaluated in terms of changes in the membrane surface area and permeability.

125 In general, the membrane surface area of olfactory and visual projection

126 an LC elasticity-induced expansion of lipid membrane surface area of up to 3% and conservation of th

127 For example, changes in membrane surface area or dielectric properties can modif

128 rifugation conditions, as well as by varying membrane surface area or membrane fouling, the filtrate

129 nt volume while they increase their apparent membrane surface area upon aspiration.

130 llars each cell faces varies with its plasma membrane surface area, despite their large population an

131 ets, which are untwisted and lie flat on the membrane surface as amyloid-like fibrils.

132 e found that PopB interacts with PopD on the membrane surface as determined by excitation energy migr

133 have a high potential to cause biofouling on membrane surface as the bacteria still maintain the cell

134 e the hydration water structure at the lipid membrane surface at XDMSO <0.1, lower the energetic barr

135 lement approach to model diffusion on curved membrane surfaces based on solutions to Fick's law of di

136 The membrane surface became more hydrophobic when chlorinati

137 interactions with an ensemble of cooperative membrane surface binding sites, rather than molecular cr

138 ph into the lower pH area near the dendritic membrane surface, bombykol is ejected near the receptor,

139 Cryo-EM has revealed the structures of the membrane-surface bound pre-pore and inserted-pore oligom

140 hat acidification of the local extracellular membrane surface by a light-activated proton pump recrui

141 domain (N-PTB), drives Dab2 to the platelet membrane surface by binding to sulfatides through two su

142 the ability of Sec7 to activate Arf1 on the membrane surface by facilitating membrane insertion of t

143 individual pH-sensitive fluorophores at the membrane surface by fluorescence correlation spectroscop

144 ndicating the faithful representation of the membrane surface by the model.

145 ory pathways promote kinetic proofreading of membrane surfaces by Rab GTPases, and permit accumulatio

146 compartment, or even to subdomains (e.g., a membrane surface), by adding signal sequences or fusing

147 ressure, which if unbalanced on the opposite membrane surface can dramatically increase membrane curv

148 es since accumulation of contaminants to the membrane surface can lead to fouling, performance declin

149 Lipid membrane surfaces can act as proton-collecting antennae,

150 nium species valence and size in relation to membrane surface charge and pore size) and (ii) concentr

151 osomes, which demonstrated the importance of membrane surface charge and the presence of the glucosyl

152 face roughness were also maintained, and the membrane surface charge became positive after functional

153 ge Chol-driven increase in lipid packing and membrane surface charge density.

154 Modulating membrane surface charge provides an effective way of inv

155 We have used membrane surface charge to modulate the structural dynam

156 stigate the effects of lipid chain disorder, membrane surface charge, and intrinsic negative curvatur

157 tive gramicidin A channel as a sensor of the membrane surface charge, we studied interactions of olig

158 and varies its orientation according to the membrane surface charge.

159 we show that by controlling the liquid cell membrane surface chemistry and electron beam conditions,

160 However, increasing the mitochondrial inner membrane surface comprises an alternative mechanism for

161 ALDI imaging demonstrated that the abluminal membrane surface consists more of polysulfone than polyv

162 id bilayer in order to elucidate the role of membrane surface curvature in modulating the peptide str

163 l ensemble of APP are strongly influenced by membrane surface curvature.

164 species signifying initiation of biofilms on membrane surfaces, demonstrated by specific DESI MS sign

165 that the binding and fibril formation on the membrane surface depends on the composition of the bilay

166 the allosteric helices, with respect to the membrane surface direction.

167 e than polyvinylpyrrolidone, and the luminal membrane surface displayed more PVP than PS.

168 olution, as compared with association at the membrane surface, displays considerably larger binding c

169 olarization to control the developing apical membrane surface during blood vessel tubulogenesis in 3D

170 ane interactions that retains dynamin on the membrane surface during the GTP hydrolysis cycle.

171 Herein, we report that membrane surface E-cadherin-expressing prostate cancer c

172 Near the membrane surface, electrostatic interactions with the li

173 (perfluorodecyltrichlorosilane) to lower the membrane surface energy.

174 form of active deformation, we find that the membrane surface exceeds by a factor of two the amount o

175 onal diffusion of the PH domain on the lipid membrane surface exhibit transient subdiffusion, with an

176 tanding of the interactions of proteins with membrane surfaces exists because these questions are ina

177 nstrate that active transport to the capture membrane surface expedites antibody-antigen binding.

178 tes such as APP are shed close to the plasma membrane surface following an "N-like" chain trace.

179 rientate both substrate cavities towards the membrane surface for efficient substrate transit between

180 l, may pave the way to generate an increased membrane surface for interaction with monocytes and neut

181 MPs are procoagulant because they provide a membrane surface for the assembly of components of the c

182 le a two-dimensional "hopping" search of the membrane surface for the rare PIP3 target lipid.

183 ium to provide photoreceptor cells with vast membrane surfaces for efficient light capture.

184 rand RNA viruses utilize various subcellular membrane surfaces for replication.

185 ows the subsequent reactant spillover on the membrane surface from the catalyst bed took place due to

186 Dimerization only occurs on the membrane surface; H-Ras is strictly monomeric at compara

187 ilic MAG2 helix was found to lie flat on the membrane surface in 1,2-dimyristoyl-sn-glycero-3-phospha

188 t allows cells to be maintained on the upper membrane surface in a thin layer of fluid while media is

189 PH-domain orientation from proximity at the membrane surface in full-length dynamin.

190 ased on estimated thicknesses of USLs at the membrane surface in real samples of nerve endings were e

191 ory subunit, factor Va (fVa), assembled on a membrane surface in the presence of divalent metal ions.

192 that the remote site is oriented toward the membrane surface in vivo, we hypothesize that its cognat

193 y important role in providing a procoagulant membrane surface in vivo.

194 at Gea1 and Gea2 prefer neutral over anionic membrane surfaces in vitro, consistent with their locali

195 tions for processes that take place at lipid membrane surfaces, including molecular recognition, bind

196 ng by developing a killing and self-cleaning membrane surface incorporating antibacterial silver nano

197 on changes in cholesterol reactivity at the membrane surface independently of the overall cholestero

198 he smaller defects found on flat and concave membrane surfaces inhibit folding by kinetically trappin

199 ns are linked by a helix that runs along the membrane surface interacting with the phospholipid head

200 of a membrane fold, which shapes the entire membrane surface into a flat double-membrane sheet.

201 that eukaryotic cells are able to convert a membrane surface into a high-definition lipid-signaling

202 The localization of His-379 on the lumenal membrane surface is consistent with a role for this inva

203 ments confirm that the zeta-potential of the membrane surface is converted from negative (non-functio

204 we present evidence that adhesion to the UF membrane surface is mediated by cell-surface macromolecu

205 Modification of the membrane surface is one route to mitigating membrane fou

206 er chlorine uptake, and (vi) scission at the membrane surface is unrepresentative of volume-averaged

207 studies showing that proton diffusion along membrane surfaces is time- and length-scale dependent.

208 previously believed to be exposed above the membrane surface, is also membrane associated, suggestin

209 s lowered the K(m) for diacylglycerol at the membrane surface (K(m)((surf))), and worked synergistica

210 The gold nanoparticles exhibit a complete membrane surface layer and biological characteristics of

211 formation and suppresses fiber growth on the membrane surface, leading to leakage.

212 Intriguingly, oligomerization of HIV-Tat on membrane surfaces leads to the formation of membrane por

213 The presence of SMP on the membrane surface led to higher rejection of MS2 due to b

214 ein levels, reduced glycosylation, and lower membrane surface levels of hCaV3.3 when expressed in hum

215 weaker and nonspecific binding of Cu(II) to membrane-surface lipid phosphates and the extent of the

216 of cell shape are largely controlled by the membrane surface load and membrane bending rigidity, and

217 Membrane surface localized endonuclease EndA of the pulm

218 voltage-gated currents from channels on the membrane surface (membrane clock) with rhythmic Ca(2+) r

219 eability, which provides a new dimension for membrane surface modification.

220 by making the electrostatic potential at the membrane surface more negative, while decreasing the pen

221 ber and large size of milk fat globules, the membrane surface needed for their release might exceed t

222 nced membrane performance through increasing membrane surface negativity and decreasing the formation

223 g that macropinocytosis and recycling to the membrane surface occur during JAM-A redistribution.

224 These negatively curved membrane surfaces occur at the base of the cell division

225 to generate ratiometric images of the plasma membrane surface of Bright Yellow 2 tobacco (Nicotiana t

226 tween the peptide and the negatively charged membrane surface of cancer cells.

227 ugh hydrophobic interactions on the external membrane surface of pneumococcal cells.

228 t cells innervate the entire somato-denditic membrane surface of principal neurons, the spike control

229 nity to the same homologous cavity as on the membrane surface of SERCA1a.

230 fer protein plastocyanin (Pc) to the lumenal membrane surface of the cytb6f complex using a Pc-functi

231 ophobic extension that lies on the cytosolic membrane surface of the lysosome, where it interacts wit

232 olymerization of actin filaments against the membrane surfaces of the aperture's edges.

233 or CD86 and CD28 (Signal 2) at the opposing membrane surfaces of the interacting cells.

234 nsertion depth and orientation relative to a membrane surface) of ganglioside GM1 in biologically rel

235 The membrane surface offers a potential platform for the cat

236 or building penetrated channels on vesicular membrane surface often involve regulating the solvent po

237 of surface morphology and surface energy on membrane surface omniphobicity were systematically inves

238 DAMTS-4_v1 was found to bind to the synovial membrane surface on cryosections, and the protein was de

239 antimicrobial activity compared to the GOTI membrane surface or the support membrane alone.

240 e quantitatively explained by the changes in membrane surface potential due to exclusion of kosmotrop

241 well as the influence of pH, ionic strength, membrane surface potential, lipid saturation, and urea o

242 theory revealed an underlying dependence on membrane surface potential.

243 that phenolics studied here are bounded to a membrane surface predominantly via hydrogen bonds, while

244 holipid surfaces, it is instead inhibited by membrane surfaces prepared directly from the plasma memb

245 Gea2 toggle roles in the cytosol and at the membrane surface, preventing membrane binding in the abs

246 ions of electrochemically produced HP on the membrane surface prevents bacterial attachment, thus ens

247 s, and prevents the biofilm formation on the membrane surface, producing excellent antimicrobial acti

248 anionic, cationic, and nonionic polymers) on membrane surface properties and fouling.

249 avage at downstream sites is accomplished by membrane surface proteases or extracellular soluble prot

250 study vesicle release, plasma and flagellar membrane surface proteins were vectorially pulse-labeled

251 We screened Leptospira outer membrane/surface proteins for their ability to activate/

252 reased amount of the enzyme localized to the membrane surface rather than with a loss of activity or

253 ates signals from upstream ErbB2/3 and CXCR4 membrane surface receptors.

254 Bacterial biofilm formation on membrane surfaces remains a serious challenge in water t

255 he outer and inner poly(benzyl methacrylate) membrane surface, respectively.

256 e-stranded oligoprobes functionalized on the membrane surface resulting in the formation of a cation

257 s to negatively charged phosphatidylglycerol membrane surfaces results in a higher ordered membrane s

258 Immobilization studies of lysozyme on the membrane surface reveal an up to six times higher lysozy

259 microscopic ligand concentration within the membrane surface solvation layer may exceed that in bulk

260 On the lumenal membrane surface, subunit f establishes direct contact b

261 ibution of adhesion forces for the different membrane surfaces suggest that the antifouling propertie

262 to have maximal catalytic activity near the membrane surface suggests that these conformational chan

263 on analysis approach, we show a reduction in membrane surface tension and increased membrane undulati

264 , we predict regions of osmotic pressure and membrane-surface tension that produce successful engulfm

265 kness is minimal, Ca(2+) stays longer on the membrane surface than K(+) or Na(+), consequently leadin

266 TmMreB assembles into double filaments on a membrane surface that can induce curvature.

267 t dynamic, helix orientation parallel to the membrane surface that satisfies the amphiphatic nature o

268 n, the fraction of peptides adsorbing to the membrane surface that successfully intercalate in the bi

269 use dissolved ions decrease the field at the membrane surface, the flow decreases upon increasing the

270 rp1 self-assembly and GTPase activity at the membrane surface, the mechanism by which CL functions in

271 ting from the accumulation of charges at the membrane surfaces; the transmembrane potential, determin

272 After CTX bind to the membrane surface, they are internalized to intracellular

273 and association of the F3 subdomain with the membrane surface through a large, interdomain conformati

274 initial stages of recruiting protein to the membrane surface through non-specific electrostatic inte

275 cated that Ras undergoes dimerization at the membrane surface through protein-protein interactions.

276 Here, we report that H-Ras forms a dimer on membrane surfaces through a protein-protein binding inte

277 thic helix is aligned nearly parallel to the membrane surface (tilt angle approximately 77 degrees )

278 phatidylserine (PS) distributed at the outer membrane surface to resemble apoptotic bodies and phosph

279 es rectangular, with low OTP values from the membrane surface to the depth of C9, and high values in

280 ne tubes displaying planar and highly curved membrane surfaces to analyze intrinsic membrane curvatur

281 inity-mapping AFM method directly correlates membrane surface topography with Pc-cytb6f interactions,

282 compartments, correct membranes, and correct membrane surfaces/topologies, involves multiple pathways

283 sed to identify an entropy gradient from the membrane surface toward the bulk water.

284 The membrane surface was first coated with polydopamine (PDA

285 the number of live bacteria attached to the membrane surface was over 90% less than that of control

286 LC searches for GPI-anchored proteins on the membrane surface, we measured residence times of single

287 disrupting the water network near the lipid membrane surface, weakening the cohesion between water a

288 Unexpectedly, the virus and membrane surfaces were located approximately 50 A apart,

289 curvature, both peptides remain flat on the membrane surface, when assessed both alone and in a 1:1

290 NTs adhere to the postsynaptic membrane surface whenever the ligand-binding sites of th

291 h cytoplasmic domain of CLS from the anionic membrane surface, which enabled subsequent association o

292 elles) and adherence of graft-polymer to the membrane surface, which facilitates grafting and reduces

293 imply interactions between tr-CYP2B4 and the membrane surface, which might assist in CYP2B4-cytb5 com

294 How to reconcile this high affinity to the membrane surface with high proton mobility is unclear.

295 nd irreversible binding of the Cu-NPs to the membrane surface with SEM and XPS after exposing the mem

296 transglutaminase (TG2), thereby endowing the membrane surfaces with anti-inflammatory properties.

297 in which the sheets are connected by twisted membrane surfaces with helical edges of left- or right-h

298 nd uninfected T cells contain interdigitated membrane surfaces, with T cell filopodia extending towar

299 equestering the amyloid fold of curli on the membrane surface without significant accumulation of tox

300 antibody-antigen interactions at the sensing membrane surface without the need to add a label or a re