ライフサイエンスコーパス: hydrophobic

1 rface area of the K1-K10 structure is 20-25% hydrophobic.

2 of BslA is required to render the community hydrophobic.

3 y which the oxidized form of the ECP becomes hydrophobic.

4 lustrated the importance of ASO backbone and hydrophobic 2' sugar modifications and revealed that the

5 son with a round-edge (RE) PMMA IOL or an SE hydrophobic acrylic IOL (SE-Acrylic).

6 IOL calcifications also occur in hydrophobic acrylic IOLs.

7 s integrate water-soluble phenylethanoid and hydrophobic alkyl into one molecule thus are endowed wit

8 The large hydrophobic amino acid p-benzoyl phenylalanine (pBzF) wa

9 axseed protein structure since exposition of hydrophobic amino acid tyrosine was modified.

10 Here we report that engineering hydrophobic amyloidogenic repeats from a synthetic bacte

11 Our results reveal a unique hydrophobic anchor mechanism that defines a previously u

12 The "electrostatic switching/hydrophobic anchoring" mechanism of conformational modul

13 lysis to export many structurally dissimilar hydrophobic and amphipathic compounds, including antican

14 iral moieties, resulting in a combination of hydrophobic and auxiliary pocket effects that yielded hi

15 dy shows that increasing segregation between hydrophobic and cationic moieties in these polymeric mim

16 coiled-coil dimer pairing is mainly based on hydrophobic and electrostatic interactions between resid

17 ation facilitated controlled release of both hydrophobic and hydrophilic drugs.

18 gned and synthesized by interconnecting both hydrophobic and hydrophilic molecular nanoparticles in p

19 potential of a novel formulation for coating hydrophobic and hydrophilic peptides onto MN devices and

20 various shapes and sizes by virtue of their hydrophobic and hydrophilic segments.

21 elix form trimeric cores of opposite nature (hydrophobic and hydrophilic, respectively).

22 which, in part, render the bilayer extremely hydrophobic and impermeable to external insults, includi

23 block copolymers made of sequence-controlled hydrophobic and ionizable monomers on the inner surface

24 The UBPs form based on hydrophobic and packing forces, as opposed to complement

25 e at the second position of the peptide, and hydrophobic and polar amino acids at the C-terminal end.

26 ility of --CH3- or -C-C-PO4- species through hydrophobic and/or cation-pi associations between green

27 ding van der Waals', ionic, carbonyl, metal, hydrophobic, and halogen bond contacts, and hydrogen bon

28 mpounds tend to be smaller, more rigid, more hydrophobic, and more drug-like than non-allosteric comp

29 using a novel composite porous membrane and hydrophobic anode.

30 h also depended on their ability to transfer hydrophobic antimicrobial constituents to the separated

31 virucidal activity of a region that combines hydrophobic-at-interface membrane-proximal external regi

32 eams and emulsions to incorporate the highly hydrophobic ATRA drug.

33 rmulation that is suitable for MN coating of hydrophobic auto-antigen peptides currently being invest

34 n of paper-based microfluidics by patterning hydrophobic barriers using a desktop pen plotter integra

35 ir water-resistant capabilities for creating hydrophobic barriers.

36 antially increased intrahepatic retention of hydrophobic BAs and decreased hepatic expression of tumo

37 of BH3-only proteins with both the canonical hydrophobic binding groove (alpha2-5) and alpha6 at the

38 the signal sequence is extending beyond its hydrophobic binding groove of the SRP M domain towards t

39 molecules can be challenging owing to large, hydrophobic binding surfaces.

40 ngly, in all three structures, the bulky and hydrophobic BP pyrenyl residue is entirely solvent-expos

41 (alpha-olefinate)s (xPAOs) as a new class of hydrophobic building block for amphiphilic materials, an

42 ng factors that compensate for the dearth of hydrophobic burial include shorter and stronger H-bonds,

43 simply distinguishes between hydrophilic and hydrophobic, but fine-tuning of the microenvironment is

44 Ubiquinone-10 is extremely hydrophobic, but in complex I the binding site for its r

45 ncreasing carbonization was explained by the hydrophobic carbonaceous matrix acting like a filter fav

46 Cyclodextrins, provide a hydrophobic cavity in the core of their structure while

47 Arbidol binds in a hydrophobic cavity in the HA trimer stem at the interfac

48 The association of a hydrophobic cavity of CDs with metal ions or various ino

49 ability of burying their lipid chains in the hydrophobic cavity of TLR2 and, in some cases, TLR1, at

50 d helix S6 of a neighbouring subunit, form a hydrophobic cavity to house the agonist, suggesting a di

51 lipopolysaccharide and traffic it along the hydrophobic cavity toward the transporter's periplasmic

52 lycolipids identified to date consist of two hydrophobic chains and an alpha-glycoside in which the 2

53 ure revealed that HO-2 binds myristate via a hydrophobic channel adjacent to the heme-binding pocket.

54 esults using structural data, which show the hydrophobic channel is interrupted by a highly charged r

55 enter of the PD-L1 homodimer, filling a deep hydrophobic channel-like pocket between two PD-L1 molecu

56 m membrane to membrane, our findings support hydrophobic channeling within membranes as a means of ce

57 molecular description of the operation of a hydrophobic clamp in triosephosphate isomerase.

58 Asn-110 and Asn-137 form a highly conserved hydrophobic cleft interacting with the core trisaccharid

59 In contrast, NH2-K(Boc)LVFF-CONH2 undergoes hydrophobic collapse at a low concentration, followed by

60 e cotranslational folding sites initiated by hydrophobic collapse for an unstructured and two globula

61 (II) in aqueous samples was converted into a hydrophobic complex of copper(II) diethyldithiocarbamate

62 ature of the hydrophilic PSs and that of the hydrophobic components, of linkers, targeting groups and

63 Since lycopene is a hydrophobic compound it is not expected to appear in the

64 The perfluorocarbon chain repels hydrophobic compounds and its oleophobicity increases wi

65 tioning of polar constituents, proteins, and hydrophobic constituents in three phases comprising of w

66 espread biological role is providing a rigid hydrophobic contact surface under the undecorated side o

67 om a variety of conformations with different hydrophobic contact surfaces that interconvert on the mi

68 ons involving 11 hydrogen bonds and numerous hydrophobic contacts account for stable complex formatio

69 H-1-PGC1alpha complex, which depicts several hydrophobic contacts and a strong charge clamp at the in

70 t, anchoring the CTD in place and permitting hydrophobic contacts between FtsZ residues Ile-374, Pro-

71 own (1)O2 scavenger, was incorporated in the hydrophobic core of amphiphilic copolymer micelles, and

72 Carotenoids can accommodate into the hydrophobic core of cyclodextrins and therefore, they ar

73 N-terminus of the peptide backbone near the hydrophobic core of cylindrical nanofibers leads to stro

74 issense mutations disrupt the folding of the hydrophobic core of hCDC73-NTD, while others such as the

75 ne-conjugated acyl-group of ACP occupies the hydrophobic core of ISD11, explaining the basis of ACP s

76 ile procedure is used for reconstituting the hydrophobic core of LDLs with a binary fatty acid mixtur

77 hrough JMJD6 interactions with the conserved hydrophobic core of the ET domain, and reinforced by ele

78 In contrast, the N-terminal hydrophobic core showed extremely slow solvent exchange,

79 ved along the peptide backbone away from the hydrophobic core, the interactions with dodecanoic acid

80 self-assembly does not entail formation of a hydrophobic core.

81 g from the interaction between the channels' hydrophobic cores and that of the lipid bilayer.

82 cycles lack regular secondary structures and hydrophobic cores, and can contain local structures not

83 tabilizes a mobile C-terminal helix inside a hydrophobic crevice of NCS-1 to impede Ric8a interaction

84 The hydrophobic cross-linkers stabilize the fold by macrocyc

85 ue to the monodispersity and symmetry of the hydrophobic dendritic block, which significantly simplif

86 Amphiphilic JDs consist of hydrophobic dendrons connected to hydrophilic dendrons a

87 ith electrodes utilizing PEDOT-C14, a highly hydrophobic derivative of poly(3,4-ethylenedioxythiophen

88 mbly displays the typical characteristics of hydrophobic desolvation processes, and detailed analysis

89 the as-formed Ag-NW thin film with a dense, hydrophobic dodecanethiol layer, the stability of the Ag

90 anchored (TA) proteins, bearing a C-terminal hydrophobic domain that is essential for their membrane

91 antimicrobial constituents to the separated hydrophobic domain.

92 Our data reveal that elastin-like hydrophobic domains are composed of transient beta-turns

93 ifferences between charged nucleic acids and hydrophobic drugs have hindered entrapment of both compo

94 reproducible method of loading micelles with hydrophobic drugs.

95 self-assembles to form long fibrils with the hydrophobic edge and histidine residues extending in an

96 Hydrophobic effects appeared to enhance binding, as many

97 static interactions dominated at pH 7, while hydrophobic effects were the main force at pH 2.

98 <F127<P123, indicating the importance of the hydrophobic environment for the colorimetric transition

99 ructural and genetic analyses, that a unique hydrophobic environment in the catalytic space of gp17-a

100 tions between peptides and lipids within the hydrophobic environment of a membrane.

101 how hydrophilic nanostructures reside in the hydrophobic environment of the membrane.

102 ted to be unstable in either an aqueous or a hydrophobic environment.

103 ling and molecular simulations reveal unique hydrophobic environments near the arginine CDR mutations

104 y charged RNA-binding tunnel with a separate hydrophobic extension that unexpectedly engages the cap

105 nd cellular mutational analysis revealed the hydrophobic face of two alpha-helices to be critical for

106 trate that PgP/pDNA polyplexes loaded with a hydrophobic fluorescent dye are retained in local neural

107 lining the interplay between hydrophilic and hydrophobic forces in molecular self-assembly.

108 le surface model describes how curvature and hydrophobic forces lead to the emergence of new protein

109 e folding and binding of random sequences of hydrophobic ([Formula: see text]) and polar ([Formula: s

110 s to release smaller, soluble but relatively hydrophobic fragments of protein (plasmin-generated prot

111 idues, V102 and F99, work together to form a hydrophobic gate.

112 ated Na(+), and these results also support a hydrophobic gating mechanism for control of ion permeati

113 This hydrophobic gating mechanism has implications for CRAC c

114 uate the potential role of these residues in hydrophobic gating, Leu267 and Leu270 in human Slo2.1 we

115 Consistent with their combined role in hydrophobic gating, replacement of both Leu residues wit

116 The hydrophobic groove of the human immunodeficiency virus t

117 CDC73-NTD contains an extended hydrophobic groove on its surface that may be important

118 IncE bound to a unique and highly conserved hydrophobic groove on SNX5.

119 that direct the distribution of the leading hydrophobic groups (LHG).

120 r achieving effective encapsulation of large hydrophobic guests, including fullerenes, polycyclic aro

121 d alphaS variant added hydrophobicity to the hydrophobic half of alphaS helices, thereby stabilizing

122 ng charged for uncharged residues within the hydrophobic half of the stabilized helix not only revers

123 The classical view of hydrophobic hydration is that, in the presence of a hydr

124 We show that 5-HT locates at the hydrophobic-hydrophilic interface, below the glycerol gr

125 hilic material can macroscopically behave as hydrophobic if a surface has proper microstructured feat

126 negligible when a hydrophilic (Ser-109) or a hydrophobic (Ile-305) amino acid is mutated instead.

127 s radicals in both environments, aqueous and hydrophobic, indicating the importance of phenolic compo

128 NTH), previously thought to drive fission by hydrophobic insertion, our results show that membrane co

129 In addition to characterizing heterogeneity, Hydrophobic Interaction Chromatography (HIC) is an assay

130 In this study, a storage- and pH-sensitive hydrophobic interaction chromatography (HIC) profile cha

131 on, monitoring of foulants during multimodal hydrophobic interaction chromatography of recombinant hu

132 imary amide group (Q side chain) weakens the hydrophobic interaction generated by the six cyclohexyl

133 inly through hydrogen bonding, although some hydrophobic interaction may also have been involved.

134 Hydrophobic interaction membrane chromatography, which w

135 eet contents and more chemical bonds such as hydrophobic interactions and disulfide bonds than those

136 Results indicated both hydrophobic interactions and disulfide bonds were signif

137 Further, vMIA hydrophobic interactions and ER-mitochondria contacts fa

138 e main driving forces of these interactions, hydrophobic interactions and hydrogen bonds, respectivel

139 Hydrophobic interactions are accompanied by hydrogen bon

140 onic polar groups have pronounced effects on hydrophobic interactions generated by a neighboring nonp

141 trate the importance of hydrogen bonding and hydrophobic interactions in the oligomerization of IAPP-

142 signal-anchored MAM proteins can make use of hydrophobic interactions independently of conventional E

143 ized by either electrostatic interactions or hydrophobic interactions involving the I36 hydrophobic p

144 (primary amine and primary amide) influence hydrophobic interactions of neighboring nonpolar domains

145 ersus methanol allowed quantification of the hydrophobic interactions of the beta-peptide with the no

146 to better overall shape complementarity and hydrophobic interactions with S372 and M368 on KCa3.1 an

147 Arbidol primarily makes hydrophobic interactions with the binding site but also

148 Membrane binding requires hydrophobic interactions with the lipid tails but not ch

149 sidues at V3 positions 306 and 308 to create hydrophobic interactions with the tryptophan residue at

150 one hand, such aggregates can disrupt native hydrophobic interactions, and on the other hand, they ca

151 electrostatic interactions, hydrogen bonds, hydrophobic interactions, and van der Waals interactions

152 pramolecular motifs in water are directed by hydrophobic interactions, cooperative delivery strategie

153 Sorption of the FtSs was driven by hydrophobic interactions, while the FtSaBs behave more l

154 trates important for adhesion via polyvalent hydrophobic interactions.

155 subunits, reinforcing filament stability by hydrophobic interactions.

156 rmines the degree to which charge influences hydrophobic interactions.

157 bonded dimers that sandwich together through hydrophobic interactions.

158 plete binding region anchored at each end by hydrophobic interactions.

159 hole-transport-layer covered substrates by a hydrophobic interface confined lateral crystal growth me

160 The hydrophobic interface is stabilized by apolar side chain

161 ing form along with providing a sufficiently hydrophobic interface to counteract the aqueous layer fo

162 lical portions of M2 contribute to extensive hydrophobic interfaces between AMPA receptor subunits in

163 coiled-coil heterodimer with a predominantly hydrophobic intermolecular interface; this heterodimer f

164 ailable cyclodextrins (CDs) with an inherent hydrophobic internal cavity and hydrophilic external sur

165 es, distinguished by their high content of a hydrophobic lactone.

166 ompressing the lipids to match the channel's hydrophobic length.

167 ation or long-term storage and relies on the hydrophobic ligand-binding pocket of AHR, with identical

168 zone in the paper is delimited by drawing a hydrophobic line with an inexpensive permanent marker.

169 ed with two transient helices connected by a hydrophobic linker.

170 Wnt proteins are secreted, hydrophobic, lipidated proteins found in all animals tha

171 e concave plots originate from AOs in a more hydrophobic location in the micro-heterogeneous system.

172 of the protein-a cationic patch and a unique hydrophobic loop-that are essential for accessing SM in

173 w type of magnetoliposomes (MLs), containing hydrophobic magnetic-gold nanoparticles and the long wav

174 In this review, we first consider hydrophobic matching of the intramembranous proteolipid

175 Commercial superglue mostly for binding hydrophobic materials is used to strongly immobilize the

176 ater evaporation when confined between model hydrophobic materials with tunable flexibility.

177 In order for many proteins to move across hydrophobic membrane bilayers, they must be unfolded and

178 g constricting rings, helical scaffolds, and hydrophobic membrane insertions are thought to be the pr

179 entin matrix create tight biointerfaces with hydrophobic methacrylate adhesives on wet surfaces.

180 t-off curves yield information regarding the hydrophobic microenvironment surrounding the reactive AO

181 ressure forced intrusion studies of water in hydrophobic microporous materials such as zeolites and M

182 ns them, and causes the greatest increase in hydrophobic mismatch between liquid-ordered (Lo) and Ld

183 lower the energetically unfavorable residual hydrophobic mismatch between TM4 and the membrane, reduc

184 As expected, the hydrophobic modified surfaces induced the highest mass a

185 rotropes are small molecules that solubilize hydrophobic molecules in aqueous solutions.

186 of surfactant was particularly notable for a hydrophobic monomer glycidyl methacrylate combined with

187 tivated by phosphorylation of its kinase and hydrophobic motif (HM) domains.

188 Heterogeneous systems composed of hydrophobic nanoporous materials and water are capable,

189 f Wnts, Frizzleds, and SFRPs, as well as the hydrophobic nature of Wnt, poses challenges to laborator

190 marily accomplished by tuning the side-chain hydrophobic or ionic interactions.

191 Moreover, regarding a liquid droplet on hydrophobic or superhydrophobic surfaces, an approximate

192 en these surfaces are micro/nanotextured and hydrophobic, or superhydrophobic, an impacting drop can

193 philic perovskite precursor solutions on the hydrophobic organic charge-transport layers (CTLs).

194 In aqueous environments, hydrophobic organic contaminants are often associated wi

195 ngulfing of a hygroscopic particle core by a hydrophobic organic-rich phase, can explain the lack of

196 ansmembrane region of FtsLB is stabilized by hydrophobic packing and by a complex network of hydrogen

197 ding of natural proteins typically relies on hydrophobic packing, metal binding, or disulfide bond fo

198 h dimer is stabilized by interactions of one hydrophobic palmitoleic acid tail with two CRD palmitole

199 Our molecular modeling suggested that a hydrophobic patch created after TCRalpha-TCRbeta pairing

200 The specific hydrophobic patch interface adopted by K48-linked diUbq

201 a single point-site mutation at the docking hydrophobic patch of a Cu-azurin causes minor structural

202 f the catalytic domain structure, covering a hydrophobic patch on the catalytic AA9 module.

203 he helix is ejected and unravels, exposing a hydrophobic patch, which then serves as a degradation si

204 r hydrophobic interactions involving the I36 hydrophobic patch.

205 Porewater concentrations of the strongly hydrophobic PCB congeners were overestimated by up to an

206 Three decades ago, the small hydrophobic peptide Z-d-Phe-l-Phe-Gly (FIP) was shown to

207 om the Rgg family and its cognate SHP (short hydrophobic peptide).

208 ope labeling for MS1 level identification of hydrophobic peptide-ligand adducts.

209 ng butanol extraction due to accumulation of hydrophobic peptides (IC50 between 12 and 21mg/l).

210 ion to this paradox by implementing a highly hydrophobic perfluorinated anion (perfluorooctanesulfona

211 Such lipid changes point to a hydrophobic phenotype for M. tuberculosis sensu stricto.

212 omplex controls the passage of molecules via hydrophobic phenylalanine-glycine (FG) domains on nucleo

213 erged adjacent to a computationally designed hydrophobic pocket during directed evolution.

214 gages the receptor by binding to an extended hydrophobic pocket facilitated by the large outward move

215 of Glu37, a glutamate residue embedded in a hydrophobic pocket of HdeA, is important in controlling

216 models places the P-CR connector loop into a hydrophobic pocket of the catalytic core, with the coile

217 The docking of the farnesyl group to the hydrophobic pockets located at both CaM lobes further en

218 We find that even short hydrophobic polar (HP) chains can collapse into relative

219 bicity, in situ passive sampling of strongly hydrophobic polychlorinated biphenyls (PCBs) is still ch

220 It was found that increasing the hydrophobic polyester content in the hydrogel reduced th

221 Plants accumulate a family of hydrophobic polymers known as polyprenols, yet how they

222 the substrate proteins they translocate via hydrophobic pore loops and cleft structures called clamp

223 This layer is covered by a hydrophobic porous Teflon membrane used as an additional

224 ion by bringing together a hydrophilic and a hydrophobic precursor, which leads to repeated droplet d

225 ved effect was an increased affinity towards hydrophobic probes in the presence of all co-solutes but

226 Here we report an investigation into the hydrophobic properties of the exopolysaccharide produced

227 oods for their nonflammable, lipophobic, and hydrophobic properties.

228 spectroscopy applying stable hydrophilic and hydrophobic radicals is advantageous, especially for cha

229 re easy to assemble and permit entrapment of hydrophobic redox molecules in aqueous solution.

230 When a short hydrophobic region is added to a sequence that directly

231 ar protein homeostasis by binding to exposed hydrophobic regions of incompletely folded or aggregated

232 mational change that lead to the exposure of hydrophobic regions responsible for target protein recog

233 rface charges and increased accessibility of hydrophobic residues (including the nuclear export seque

234 the first two residue sidechains complement hydrophobic residues around the active site, while the t

235 receptors containing each of four different hydrophobic residues at position 195 served as input dat

236 data support a model in which small neutral hydrophobic residues facilitate the post-translational c

237 Several aromatic and hydrophobic residues in pore helix 1, helices S5 and S6,

238 ic domain form a latch-like interaction with hydrophobic residues in the lid.

239 diates, each with a nonnative arrangement of hydrophobic residues in the MDM2 binding cleft, control

240 eed other intrinsically disordered proteins, hydrophobic residues likely drive Cdc42-ACK binding.

241 Resveratrol and curcumin bind only to the hydrophobic residues near peptide termini.

242 (iv) Surface hydrophobic residues of CD1 are involved in heterogeneou

243 -directed mutagenesis on the surface-exposed hydrophobic residues of pvLAAD INS, and we found that th

244 rane-proximal external region aromatics with hydrophobic residues of the transmembrane domain, and co

245 econfiguration rate is slow enough to expose hydrophobic residues on the same time scale that bimolec

246 Residues P193 and W222 comprise a series of hydrophobic residues surrounding the cofactor binding si

247 s simultaneous substitution of four aromatic/hydrophobic residues with Ala dramatically impairs both

248 ulations, here we identified single aromatic/hydrophobic residues within the amyloid core IAPP region

249 site-directed mutagenesis of outward-facing hydrophobic residues within the transmembrane region of

250 nus side of the HA PCS (P2 position) avoided hydrophobic residues, whereas the P3 position avoided hy

251 ly of AT1R homomers with a specific focus on hydrophobic residues.

252 a central cavity containing highly conserved hydrophobic residues.

253 e barrel core is fastened by three layers of hydrophobic residues.

254 The GPE contained the hydrophobic room-temperature ionic liquid (RTIL) trihexy

255 hydration state of the deep, well-accessible hydrophobic S1' specificity pocket of the metalloproteas

256 ructure of most potent sweeteners combines a hydrophobic scaffold functionalized by a limited number

257 Hydrophobic self-assembled monolayers on gold or silicon

258 rease in polar side chains and a decrease in hydrophobic side chains lining the vestibule, and this w

259 ruitment site that normally accommodates the hydrophobic sidechains of a canonical D-site, retaining

260 ynthesis the nanocapsules can be loaded with hydrophobic small molecules and post self-assembly under

261 Their lipid cores can be loaded with hydrophobic small molecules by passive diffusion.

262 nanoporphyrin micelles (NPM), the extremely hydrophobic SN-38 was successfully encapsulated into NPM

263 Hydrophobic solid substances like graphite and carbon na

264 obic hydration is that, in the presence of a hydrophobic solute, water forms transient microscopic "i

265 t for the enhanced hydrogen bonding around a hydrophobic solute.

266 cleated nanodroplets for nanoextraction of a hydrophobic solute.

267 retching mode of HDO water near small purely hydrophobic solutes (methane, ethane, krypton, and xenon

268 Sarcoma Virus (RSV), CA carries a short and hydrophobic spacer peptide (SP) at its C-terminus early

269 viously shown that this is in part because a hydrophobic statin with a long half-life is necessary.

270 nism underlying this effect is unclear, i.e. hydrophobic/steric effects versus electrostatic effects.

271 e, degenerate, interchangeable, linear or 3D hydrophobic stretches that become available because of t

272 strongly compromises the water-repellency of hydrophobic structures, this failure can be minimized by

273 ibitors; PJ34 inserts a flexible moiety into hydrophobic subpockets in various ADP-ribosyltransferase

274 water droplet surface suggests that strongly hydrophobic substituents determine the reactivity of Cri

275 Combinatorial mutagenesis demonstrated that hydrophobic substitutions were tolerated but polar or ch

276 e transporters that transport amphipathic or hydrophobic substrates in a detergent-free native or art

277 This effect is more significant for the hydrophobic surface compared with the hydrophilic ones,

278 Favorable hydrophobic surface interactions between nC60-stir and 7

279 th nanogold-conjugated CBM3, which binds the hydrophobic surface of crystalline cellulose, was infreq

280 er-layer shedding depend on interaction of a hydrophobic surface on VP5* with the membrane bilayer an

281 ed by the cohesion-tension theory by coating hydrophobic surfaces and nanobubbles, thereby keeping th

282 show that angiosperm xylem contains abundant hydrophobic surfaces as well as insoluble lipid surfacta

283 his work, the interaction of soy sauces with hydrophobic surfaces has been analyzed.

284 cular kinetic analyses of water spreading on hydrophobic surfaces via molecular dynamics simulation.

285 ic energy from the motions of water drops on hydrophobic surfaces, and thus, the resulting schemes in

286 into relatively compact structures, exposing hydrophobic surfaces.

287 S100A11, a dimeric EF-hand protein with two hydrophobic target binding sites.

288 o dye, at pH 6.5, and then extraction of the hydrophobic ternary complexes formed in presence of cety

289 ted from electrically conductive, insulated, hydrophobic textiles, but the concept can be extended to

290 is lamellar and determined that its average hydrophobic thickness is 24.3 +/- 0.9 Angstroms (A).

291 wering of the kinetic barrier imposed by the hydrophobic thickness of the membrane.

292 Thus, vaccines carrying hydrophobic TLR2 ligands would interact with particular

293 ted mainly Abeta dimer and trimer formation, hydrophobic toluene mainly affected formation of larger

294 l-anchored membrane proteins with moderately hydrophobic transmembrane domains.

295 Prp40 homolog A (HsPrp40A), which contains a hydrophobic triad W1L4L8 that is known to be important i

296 ike a lid, opening and closing access to the hydrophobic tunnel, which accommodates the aliphatic tal

297 D is separated from a cooled distillate by a hydrophobic, water-excluding membrane.

298 lic working area of the paper delimited with hydrophobic wax.

299 , the bulk polymer itself is elastomeric and hydrophobic while its superhydrophilic surface propertie

300 rpret drop movements on both hydrophilic and hydrophobic wires, with the support of experimental resu