ライフサイエンスコーパス: hydrophobic

1 en bonding) and sp(3)C-sp(2)C (CH-pai and/or hydrophobic).

2 icles are coated with thiolated dextran, and hydrophobic acetal groups are installed through direct c

3 The new hydrophobic acrylic Vivinex XY1 IOL showed significantly

4 ration of self-healing in alternating/random hydrophobic acrylic-based copolymers in the presence of

5 the N6-methyl group is accommodated within a hydrophobic active-site subpocket explaining why N6-meth

6 The relatively hydrophobic adhesives that achieved equivalent/enhanced

7 me has been shown to bind on the surfaces of hydrophobic aggregates, such as detergent micelles, lipo

8 nic interface, reminiscent of the canonical, hydrophobic air-water interface.

9 d gate in the ion-conducting pore, formed by hydrophobic amino acid side chains, located ~60 angstrom

10 rved PhiXXPhiPhi motifs (with Phi denoting a hydrophobic amino acid) in AD1 and AD2.

11 T of Bacillus halodurans is a transporter of hydrophobic amino acids and a homologue of the eukaryoti

12 he isostere of lopinavir in combination with hydrophobic amino acids on the opposite P2/P2' position.

13 Conserved hydrophobic amino acids within the cysteine-rich region

14 Together with other hydrophobic amino acids, the phenylalanines act as the c

15 up to six monosaccharide units attached to a hydrophobic amino-pentyl linker, a construct not expecte

16 to predict the bilayer-perturbing potency of hydrophobic/amphiphilic drugs candidates.

17 surfaces that display alternating stacks of hydrophobic and charged groups.

18 folded polypeptide chains, even those with a hydrophobic and charged sequence composition typical of

19 articles was tuned by varying the lengths of hydrophobic and hydrophilic building blocks.

20 s a metal and a superfine ionomer layer with hydrophobic and hydrophilic functionalities that extend

21 igand structure interacted directly with the hydrophobic and hydrophilic halves of the CA II active s

22 ristine graphene flakes possess well-defined hydrophobic and hydrophilic regions: the basal plane and

23 on bioproduction was observed with both the hydrophobic and hydrophilic strategies.

24 ol hydrogen-bonding networks confined within hydrophobic and hydrophilic zeolite catalysts modify rea

25 the encounter complex, transient nonspecific hydrophobic and long-range electrostatic contacts form b

26 wer and more convergent repertoire with more hydrophobic and strongly interacting amino acid residues

27 The two faces of the beta-sheet core are hydrophobic and surrounded by the membrane-mimicking env

28 We found that local clustering of hydrophobic and/or charged residues leads to significant

29 ne is stabilizing, our results indicate that hydrophobic and/or electrostatic effects in the cavity a

30 dies suggest that activators use nonspecific hydrophobic and/or electrostatic interactions to bind to

31 enrichment strategies (i.e., hydrophilic and hydrophobic) and a liquid handling platform allowing for

32 Interactions of sp(3)C with itself (hydrophobic) and with sp(2)N are modestly favorable, whi

33 Surprisingly, these interactions are largely hydrophobic, and they do not include the previously iden

34 ferent wetting properties of hydrophilic and hydrophobic areas in the channels, we improve the extrac

35 ckets, leading to a lower capacity to entrap hydrophobic aroma compounds.

36 ted BA-induced liver pathology and decreased hydrophobic BA levels in an MLL4-dependent manner.

37 he licorice root and possesses a triterpenic hydrophobic backbone and a hydrophilic headgroup built f

38 hibition by posttranslational sumoylation, a hydrophobic barrier within the pore, and a low open prob

39 quorum-sensing proteins across the membrane hydrophobic barrier.

40 Hydrophobic Beta zeolites containing framework Sn atoms

41 nspecific ionic interactions involving basic-hydrophobic (BH) sites but the mechanism of myosin 1s di

42 Hydrophobic C2 substituents of sufficient size generally

43 illararenes (PAs; e.g. rigid, capacious, and hydrophobic cavities, as well as exposed functional grou

44 strategy highlights the crucial role of BLG hydrophobic cavity and opens up new possibilities for th

45 favorable Van der Waals interactions with a hydrophobic cavity at the dimerization site.

46 -based molecule and a beta-cyclodextrin (CD) hydrophobic cavity for asymmetric catalytic applications

47 turally simple BODIPY derivatives within the hydrophobic cavity of a water-soluble, flexible Pd(II)(6

48 hat one to two water molecules can enter the hydrophobic cavity of alpha(3)Y and hydrogen bond to Y(3

49 usion of a d-glucosamine derivative into the hydrophobic cavity of beta-CD increased its surface area

50 The interface formed a conserved hydrophobic cavity suitable for targeted drug screening.

51 tinol, which has a high affinity for the BLG hydrophobic cavity, significantly stabilizes BLG both in

52 a host-guest study as they offer the largest hydrophobic cavity.

53 lle, pointing the farnesyl moieties into the hydrophobic center and positioning the head groups at th

54 del indicates that m102.4 targets the common hydrophobic central cavity and a hydrophilic rim on the

55 6-tetrachloroisophtalonitrile, TPN) into the hydrophobic channel and observed that the most energetic

56 Our results demonstrated that the hydrophobic character of the drug molecule allows to rap

57 While the hydrophobic character of the interaction is conserved, t

58 how that the evaluation of electrostatic and hydrophobic characters of the mabs is useful in predicti

59 d aggregation-caused quenching effect of the hydrophobic chromophores.

60 However, a stable hydrophobic clamp composed of residues I127, F310, A311,

61 e interactions of resin with protein surface hydrophobic clusters distributed across CDRs of light ch

62 de the secreted proteins BslA, which forms a hydrophobic coat over the biofilm, and TasA, which forms

63 Furthermore, these highly stable and hydrophobic COFs display excellent oil/water separation

64 ament displays a paucity of salt bridges and hydrophobic complementarity between the TnT tail (TnT1)

65 elical hydrocarbons as rigid scaffolds or as hydrophobic components in soft materials.

66 toside, which preserved both hydrophilic and hydrophobic components of the SDBC and allows the retent

67 For 11 polar and moderately hydrophobic compounds (-0.07 <= logK(OW) <= 3.13), 90% o

68 Removal of specific hydrophobic compounds increased, indicating that both hy

69 a subtle inhibitory effect on the binding of hydrophobic compounds to alpha-amylase, thereby increasi

70 ively reduces the headspace concentration of hydrophobic compounds.

71 l similar but with a higher degree of native hydrophobic contact formation in the transition state of

72 he enhancement of self-healing efficiency of hydrophobic copolymers by a factor of three.

73 DOM aggregates are dynamic, consisting of a hydrophobic core and amphiphilic exterior.

74 In addition, the hydrophobic core and endogenous atheroma-targeting abili

75 te taken by pumped protons to traverse CcO's hydrophobic core and on whether bacterial and mitochondr

76 ation promotes drug release by switching the hydrophobic core into completely hydrophilic chains.

77 Unlike the hydrophobic core of pathogenic amyloids, the hydrophilic

78 ted-chitosan-zinc-insulin complexes into the hydrophobic core of PLA-PEG-PLA thermogel-copolymer mice

79 mide, with the interior water present in the hydrophobic core of the confined micellar medium in aque

80 ents showed that phenols were located in the hydrophobic core of the micelle.

81 hored to the helical scaffold by a secondary hydrophobic core, pinning down the long loops of leptin

82 k water phase, lipid interface and the lipid hydrophobic core.

83 NIPAm) (pNIPAm), held above its LCST, formed hydrophobic cores around which shells composed of NIPAm,

84 rhodamine 110 and 6G dyes paired with bulky hydrophobic counterions, which prevent dye self-quenchin

85 atal water loss by transpiration through the hydrophobic cuticle is ubiquitous in land plants, but th

86 faecal pellets and through adherence to its hydrophobic cuticle.

87 We sought to explore if PET imaging using hydrophobic cyclic peptides that partition into the cell

88 method (VA-DES-DLME) was developed based on hydrophobic deep eutectic solvent for extraction of foli

89 In this study 39 different hydrophobic deep eutectic solvents were evaluated for gr

90 demonstrated long-term stability because the hydrophobic DMIMPF(6) layer blocked moisture permeation.

91 arge binding site (1000 angstrom) with fewer hydrophobic domains that makes a challenge to identify t

92 d water and it displays both hydrophilic and hydrophobic domains, a net negative charge, and high por

93 ethods of making carrier-free nanodrugs from hydrophobic drug molecules, evaluating their performance

94 ionally high encapsulation efficiencies of a hydrophobic drug simvastatin (SV) and a photosensitizer

95 geranic acid (CAGE), for oral delivery of a hydrophobic drug, sorafenib (SRF).

96 ide range of bioactive molecules, from small hydrophobic drugs to large biomolecules such as proteins

97 mple, scalable strategy for oral delivery of hydrophobic drugs.

98 ccessful in transdermal delivery of low-dose hydrophobic drugs.

99 as well as an efficient method to solubilize hydrophobic drugs.

100 for proteins with different properties and a hydrophobic dye and describe for the first time how thes

101 As proof of principle, the effects of hydrophobic (e.g., esterification) and hydrophilic (e.g.

102 The argument that the hydrophobic effect is the primary effect driving the fol

103 vides a counterbalance to the absence of the hydrophobic effect.

104 nd [C-H...anion] interactions in addition to hydrophobic effects.

105 multimers, most show signatures of long-term hydrophobic entrenchment.

106 problem of accommodating charges in a highly hydrophobic environment while maintaining selective subs

107 o stabilize serine and threonine residues in hydrophobic environments while concomitantly providing t

108 cted by interactions between the classic I44 hydrophobic face of the distal Ub and the conserved MGF

109 d and contorted backbones, which incorporate hydrophobic fluorinated and hydrophilic sulfonic acid fu

110 CpLIP2 catalytic site via electrostatic and hydrophobic forces.

111 The lipid tails and other hydrophobic fragments form the core, with hydrophilic an

112 structure of the SepF-FtsZ complex reveals a hydrophobic FtsZ-binding pocket, which defines the SepF

113 The short-lived hydrophobic gas nitric oxide (NO) is a broadly conserved

114 t channel structure, reveal a double-barrier hydrophobic gate formed by two S6 amino acids in the cen

115 xhibited strong dewetting within the central hydrophobic gate region of the pore.

116 lved monovalent cations intracellular to the hydrophobic gate.

117 s showed that Phactr1 binding remodels PP1's hydrophobic groove, creating a new composite surface adj

118 dechlorination of trichloroethylene (TCE), a hydrophobic groundwater contaminant.

119 ors (6a, 6b, 6d, and 6e) with flexible bulky hydrophobic groups instead of the rigid polyheterocyclic

120 itates adhesion of Salmonella Typhimurium to hydrophobic host cell surfaces, and contributes to effic

121 33 C terminus revealed that it fits into the hydrophobic hot spot region of the accessible surface of

122 eptors is complex, with strong dependence on hydrophobic hot spots and networks of water-mediated hyd

123 rom ~4 to ~2 nm, orientation of monomers and hydrophobic hydration in the monomers.

124 tical for achieving interactivity, relies on hydrophobic, hydrophilic, supramolecular, and ionic inte

125 sociated islet amyloid polypeptide (IAPP), a hydrophobic-hydrophilic interface-dependent process with

126 nd Asp (charged) activate PKM2 and that Val (hydrophobic) inhibits it.

127 n and cellular uptake, tryptophan to enhance hydrophobic interaction with cell membranes, histidine t

128 tures such as membrane binding of the MA via hydrophobic interactions and exhibit several differences

129 ic model, which revealed that both polar and hydrophobic interactions are crucial for binding affinit

130 These results suggest the formation of hydrophobic interactions between polyphenols and bile ac

131 a, thioflavin-T-positive aggregates, whereas hydrophobic interactions dominate self-assembly in [R273

132 vent combinations to disrupt the H-bonds and hydrophobic interactions holding together the beta-sheet

133 ilizes the N-NTD dimers through simultaneous hydrophobic interactions with both partners, resulting i

134 he aromatic groups of SV and PpIX and strong hydrophobic interactions with the alkyl chains of the ca

135 short polymer block leading to non-covalent, hydrophobic interactions with the lipid bilayer.

136 port that 4E10 establishes electrostatic and hydrophobic interactions with the viral membrane surface

137 T domain known to be important for ionic and hydrophobic interactions with ubiquitin may have equival

138 additional stabilization compared to purely hydrophobic interactions, we infer that the six M101-F99

139 acid through a network of electrostatic and hydrophobic interactions, which provides insights into t

140 the NorA pump mediated by hydrogen bonds and hydrophobic interactions.

141 ous media by combining hydrogen bonding with hydrophobic interactions.

142 expectedly, mutating the PEP surface and the hydrophobic interface of A3G does not abolish virion pac

143 se of an electrostatic repulsion and forms a hydrophobic interface with ACE2.

144 d hormone receptors, we show that an ancient hydrophobic interface, conserved for hundreds of million

145 homodimer through N-terminal segments and a hydrophobic interface, with putative active sites within

146 acid-base chemistry, ion distributions near hydrophobic interfaces, and electric fields near the sur

147 A hydrophobic ionic liquid within the material was used to

148 levant ions from solution and injecting more hydrophobic ions into the active layer.

149 tentially involved in the degradation of the hydrophobic layer and pyrolysed organic matter, such as

150 are covered by the cuticle, an extracellular hydrophobic layer that provides protection against abiot

151 Because only two of the eight or ten hydrophobic layers are perturbed, catalytic sites can be

152 The CPSFL1 gene encodes a CRAL-TRIO hydrophobic ligand-binding (Sec14) domain protein.

153 n most cases, the interactions between short hydrophobic ligands dominate and dictate assembly outcom

154 ellular chaperones for fatty acids and other hydrophobic ligands inside cells.

155 extents are hot spots for interactions with hydrophobic ligands, lipids and ions, as well as discret

156 m) on the nonpolar cellulose surfaces and on hydrophobic lignin, and equivalent water-rich nanocluste

157 oMan-containing dendrimers, which have their hydrophobic linker connected via a thiourea group to the

158 Hydrophobic lipid modification of each peptide segment p

159 and live-cell compatible affinity probes for hydrophobic lipid species.

160 s membrane anchoring moiety, consisting of a hydrophobic loop located at the tip of two amphipathic d

161 ider a balance of curvature free energy with hydrophobic matching and demonstrate how our data suppor

162 The interaction of various factors such as hydrophobic material, smooth optic surface, and sharp po

163 f enhancing the electrostatic interaction in hydrophobic media at high temperature.

164 and the interfaces between water and air or hydrophobic media represent asymmetric environments with

165 Here, we study the hydrophobic membrane motifs of two Drosophila melanogast

166 specific sequence features and principles of hydrophobic membrane motifs that mediate their accumulat

167 oplets" with hydrophilic surface and elastic hydrophobic membrane, we developed an oil-free passive m

168 y the targeting and accumulation of specific hydrophobic, membrane-embedded proteins on LDs.

169 ips the substrate in a sequence-promiscuous, hydrophobic milieu.

170 g this region revealed that relatively small hydrophobic moieties are preferred, with 10 being the mo

171 fluorophores, followed by slow insertion of hydrophobic moieties into the lipid bilayer core.

172 design of self-immolative and crosslinkable hydrophobic moieties offer stable and high encapsulation

173 ne helices (CAPHs) with modifications to the hydrophobic moiety at the N-terminus.

174 th a p-acetamido azobenzene substituting the hydrophobic moiety present in many beta(2)-AR antagonist

175 o creating an almost impenetrable barrier to hydrophobic molecules that can otherwise pass through ph

176 offer an elegant tool to efficiently deliver hydrophobic molecules to animal models.

177 We show that a single hydrophobic mutation on the cyt cb(562) surface drastica

178 Here we show that a hydrophobic mutational ratchet systematically entrenches

179 Confining water in hydrophobic nanopores could be a way to modulate water s

180 e of poorly soluble molecules and water into hydrophobic nanopores of a host material where the lower

181 ntinuous and spontaneous liquid outflow from hydrophobic nanopores with high and stable efficiency ca

182 oparticles (NPs) confined in hydrophilic and hydrophobic nanopores.

183 water, including wetting/dewetting in narrow hydrophobic nanopores.

184 strate ultra-long release profile due to the hydrophobic nature of the linker, and as per characteris

185 Therefore, it is the hydrophobic nature of the phospholipid packing voids tha

186 nti-cancer drugs are restricted due to their hydrophobic nature, requiring use of harmful organic sol

187 Two hydrophobic negatively charged peptides triggered CCK re

188 , binding proteins are believed to transport hydrophobic odorant molecules across the aqueous lymph p

189 ples such as plasma-treated gold substrates, hydrophobic or hydrophilic self-assembled monolayers, an

190 sequence variants representing all possible hydrophobic or polar single- and double-point mutations.

191 t offers several advantages, especially when hydrophobic or volatile active agents are used.

192 generally can predict the bioaccumulation of hydrophobic organic contaminants by benthic and sessile

193 Classically, NRs are targeted via their hydrophobic, orthosteric pocket.

194 ides the first proof-of-concept that stable, hydrophobic oxidovanadium complexes retain excellent cel

195 oligomers is driven by hydrogen bonding and hydrophobic packing of the residues from the central and

196 nly a few residues in the fibrils, including hydrophobic pai-pai interactions with aromatic rings of

197 ient areas (75%), likely due to preferential hydrophobic partitioning, electrostatic interactions, an

198 the pan-group cyclic CSPs exhibit a chimeric hydrophobic patch conformation that resembles the hydrop

199 face of the distal Ub and the conserved MGF hydrophobic patch of the UBA domain.

200 Finally, we show that mutation of the hydrophobic patch prevents cyclin B1 localization to cen

201 We show that the hydrophobic patch targets Cdc13 to the yeast centrosome

202 nvestigate the substrate-docking region, the hydrophobic patch, on the fission yeast mitotic cyclin C

203 phobic patch conformation that resembles the hydrophobic patches required for both ComD1 and ComD2 bi

204 Secretions were analysed to estimate total hydrophobic peptide concentrations, presence of known AM

205 ng ligands, an ionic molecular tweezer and a hydrophobic peptide that despite their different interac

206 ds for most biomolecules except proteins and hydrophobic peptides.

207 00 ng/L (PFOS) along with longer-chain, more hydrophobic PFAS.

208 made in understating how S4 moves through a hydrophobic plug upon voltage changes, the possible heli

209 included 2-pyridyl ethers directed into the hydrophobic pocket and small carbocyclic rings accessing

210 rom unique interactions of the ligand with a hydrophobic pocket at the interface of the second extrac

211 D, which revealed a conserved horseshoe-like hydrophobic pocket formed by an unusually long loop.

212 bic ridge from one Ig1 domain inserts into a hydrophobic pocket from the opposing Ig1 domain producin

213 appears to be due to the emergence of a new hydrophobic pocket generated by the insertion of the six

214 ative allosteric substrate-binding site in a hydrophobic pocket on the enzyme surface.

215 et at the caspase-1 L2 and L2' loops bound a hydrophobic pocket within the GSDMD C-terminal domain di

216 ology modeling as a deep, sterically limited hydrophobic pocket, with the outward pointing piperidine

217 itated by hydrogen-bonding interactions in a hydrophobic pocket.

218 ane architecture, an "intrinsic ligand," and hydrophobic pockets off a pore cavity that is surprising

219 ed protein structures have a lower number of hydrophobic pockets, leading to a lower capacity to entr

220 In modern societies, biodegradation of hydrophobic pollutants generated by industry is importan

221 ion from electrospinning solutions made of a hydrophobic polymer dissolved in a water-miscible or pol

222 m selected polymers, specifically a somewhat hydrophobic polymer that was extremely effective at inhi

223 um 4-styrenesulfonate) polyelectrolytes on a hydrophobic polyvinylidene fluoride substrate.

224 l samples, which have an abundant portion of hydrophobic poorly ionizable material.

225 Confinement of water in hydrophobic pores alters its hydrogen bonding structure

226 electrostatic repulsion of chaotropes on the hydrophobic portion of the membrane.

227 the highest GLP-1 response was found with a hydrophobic positively charged peptide, pointing to the

228 hange and dilution, transformation of larger hydrophobic precursors in sediments can be a source to P

229 ors (TMF, 3.7-9.3 for L-PFOS), suggests that hydrophobic precursors in sediments undergo transformati

230 Hydrophilic and hydrophobic quasi-spherical and star-shaped gold (Au)NPs

231 wo-chain intermediate state is stabilized by hydrophobic rather than ionic interactions, as in AtLEGg

232 n of ordered water molecules confined within hydrophobic reaction pockets alters the energetics of ad

233 contributes more to the exposure (i) to more hydrophobic, recalcitrant congeners, and (ii) of adults

234 e, which is the key component in sensing the hydrophobic regions exposed to solution after protein un

235 Moreover, we pattern hydrophobic regions onto nitrocellulose using the wax pr

236 u-binding groove in the ACD also binds short hydrophobic regions within HspB1 itself, and HspB1 mutat

237 ith a glutamine residue at position +1 and a hydrophobic residue at position -1, thus elucidating the

238 NCE In this study, we identified an aromatic hydrophobic residue in foot-and-mouth disease virus (FMD

239 This study suggests that the conserved hydrophobic residue within the intracellular loop 2 of t

240 We show that variations in hydrophobic residues at the active site of class D SBLs

241 Here, we have mutated several hydrophobic residues from I360 to F370 in the S4 segment

242 on between WhiB1 and sigmaA4 is dominated by hydrophobic residues in the [4Fe-4S] cluster binding poc

243 ctric charge of the filaments, the number of hydrophobic residues in the constituent keratin polypept

244 tal structure near the A-cluster, defined by hydrophobic residues including F229, forms a cage surrou

245 from the inner leaflet and is coordinated by hydrophobic residues of the M and E transmembrane helice

246 required for Rap1A activation and identified hydrophobic residues on the surface of the RA2 domain th

247 ls an ~160- angstrom long channel lined with hydrophobic residues suitable for solubilizing multiple

248 esidue 375 mutations that mimic the bulky or hydrophobic residues typically found in simian immunodef

249 h the binding interfaces feature clusters of hydrophobic residues, overall, the protein-protein assoc

250 mbly of LC domains that are nearly devoid of hydrophobic residues, such as the 214-residue LC domain

251 with a cationic carboxy terminus depleted in hydrophobic residues.

252 epresented regions rich in proline and other hydrophobic residues.

253 positively charged residues intercalated by hydrophobic residues.

254 mer interface is formed by a small number of hydrophobic residues.

255 A hydrophobic ridge from one Ig1 domain inserts into a hyd

256 mponents, we identified that deletion of the hydrophobic rodlet layer or dihydroxynaphthalene-melanin

257 eal a second CypA-binding site formed by the hydrophobic sequence (47) GVVHGVATVA(56) , termed PreNAC

258 ng to HDAC1 with tetrahydropyran acting as a hydrophobic shield from water at the enzyme surface.

259 Like in lipid bilayers, the hydrophobic shielding in the aggregates of these disc-sh

260 romatic or heteroaromatic substituent, and a hydrophobic side chain.

261 Our findings suggest that large hydrophobic side chains occlude the pore, forming a phys

262 tent with BVM binding to an internal ring of hydrophobic side chains of L279 residues.

263 s the perfect alternation of cationic versus hydrophobic side chains, representing a significant impr

264 atural amino acids with different lengths of hydrophobic side chains.

265 inates can be tuned from superhydrophilic to hydrophobic simply by exchanging the cations; hydrophili

266 dox environments regulate cargo binding to a hydrophobic site within the cysteine-rich region of Erv4

267 on of a Hf-DBP nMOF for the co-delivery of a hydrophobic small-molecule toll-like receptor 7 agonist,

268 Additionally, reactant adsorption within hydrophobic Sn-Beta is driven by the breakup of intrapor

269 ordered H-bonding solvent network present in hydrophobic Sn-Beta stabilizes the transfer hydrogenatio

270 s rate enhancement stems from the ability of hydrophobic Sn-Beta to inhibit the formation of extended

271 eta, giving rise to higher turnover rates on hydrophobic Sn-Beta.

272 In addition, fire-induced hydrophobic soil layers, caused by condensation of pyrol

273 mably n-pai*), sp(2)C-sp(2)C (pai-pai and/or hydrophobic), sp(2)O-sp(2)N (hydrogen bonding) and sp(3)

274 se glypicans change conformation to create a hydrophobic space.

275 erature from 30 to 37 degrees C enhances the hydrophobic stabilization effects of retinol.

276 ricaprylin) owing to the tricyclic diterpene hydrophobic structure in their molecules that enables th

277 uried in multimeric interfaces to accumulate hydrophobic substitutions to levels that are not tolerat

278 ize exclusion mechanism, thus protecting the hydrophobic substrate from being wetted by the low-surfa

279 A singular hydrophobic substrate recruitment site is exposed at the

280 regate those transporters of hydrophilic and hydrophobic substrates.

281 strates, and material softening dominates on hydrophobic substrates.

282 the N53I substitution exposes an additional hydrophobic surface and that the intramolecular dynamics

283 layer and pyrolysed organic matter, such as hydrophobic surface binding proteins, laccases (AA1_1),

284 site sequesters apolar ligands via a concave hydrophobic surface in SAA oligomers.

285 Under these conditions, many hydrophobic surfaces on proteins may be transiently expo

286 physiological temperatures indicate that the hydrophobic surfactant proteins disrupt the ordered stru

287 central tunnel, accompanied by a hydrophilic-hydrophobic switch.

288 his approach could be generalized to another hydrophobic tag (HyT) degrader by demonstrating the impr

289 hybrid dental adhesives were relatively more hydrophobic than the Bis-GMA/HEMA controls.

290 n a similar manner to EspG(5), shielding the hydrophobic tip of PPE4(mt) from solvent.

291 H3-53 antibody that used a long CDRH3 with a hydrophobic tip to bridge between adjacent down RBDs, th

292 change the local nature of the surface from hydrophobic to hydrophilic(19), resulting in the pinning

293 iogenesis faces the challenge of chaperoning hydrophobic transmembrane helices for faithful membrane

294 of H3K27me3 by BAHCC1 is achieved through a hydrophobic trimethyl-L-lysine-binding 'cage' formed by

295 grates to the catalytic heme site via a long hydrophobic tunnel and displaces LeuE11 away from the fe

296 sists of seven stacked rings, with a central hydrophobic tunnel sufficiently long to span the peripla

297 ygen transport follows a single well-defined hydrophobic tunnel, formed from both enzyme and substrat

298 ytosolic domain contains a large, moderately hydrophobic vestibule that can bind a substrate's transm

299 CH-3-8 is hydrophobic with an aqueous solubility of 0.97 +/- 0.16

300 r on anode and filling the pores of MOF with hydrophobic Zn(TFSI)(2) -tris(2,2,2-trifluoroethyl)phosp