ライフサイエンスコーパス: hydrophobic interaction

1 pi-pi EDA interaction, hydrogen bonding, and hydrophobic interaction).

2 ractions (electrostatic, pi-pi stacking, and hydrophobic interactions).

3 hydrogen bonding, polymeric interaction and hydrophobic interaction.

4 n of LAE-lecithin complexes probably through hydrophobic interaction.

5 ooligosaccharides through hydrogen bonds and hydrophobic interactions.

6 lding allows formation of novel, stabilizing hydrophobic interactions.

7 brane via a combination of electrostatic and hydrophobic interactions.

8 hought to be primarily driven by nonspecific hydrophobic interactions.

9 rwhelmingly by electrostatic and slightly by hydrophobic interactions.

10 drogen bond, metal-ligand, electrostatic and hydrophobic interactions.

11 the micellization process is provided by the hydrophobic interactions.

12 ition; the contact interface is dominated by hydrophobic interactions.

13 into our understanding of the phenomenon of hydrophobic interactions.

14 phospholipid layer of the liposomal core via hydrophobic interactions.

15 stacking interactions as well as hydrophobic-hydrophobic interactions.

16 vating BovK mainly through electrostatic and hydrophobic interactions.

17 nups and is driven by both electrostatic and hydrophobic interactions.

18 ugh hydrophobic cavities or electrostatic or hydrophobic interactions.

19 trates important for adhesion via polyvalent hydrophobic interactions.

20 subunits, reinforcing filament stability by hydrophobic interactions.

21 le spots due to the interplay of hydrophilic/hydrophobic interactions.

22 itope of SF3B3 that is strongly dependent on hydrophobic interactions.

23 o acid substitutions suggested this involves hydrophobic interactions.

24 nterface, a three-helix bundle with critical hydrophobic interactions.

25 ed, and enthalpically disfavored, typical of hydrophobic interactions.

26 rmines the degree to which charge influences hydrophobic interactions.

27 The other results from hydrophobic interactions.

28 og 2 to 3, which is explained by postulating hydrophobic interactions.

29 ligand stabilization was primarily driven by hydrophobic interactions.

30 s two adjacent receptor trimers via multiple hydrophobic interactions.

31 cytochrome c through both electrostatic and hydrophobic interactions.

32 ggested that these associations are ruled by hydrophobic interactions.

33 ntegrate lipid bilayers by electrostatic and hydrophobic interactions.

34 ipid binding involves both electrostatic and hydrophobic interactions.

35 ycon showed stronger binding due to enhanced hydrophobic interactions.

36 omatic residue clustering through long-range hydrophobic interactions.

37 bonded dimers that sandwich together through hydrophobic interactions.

38 il, which is attributed to electrostatic and hydrophobic interactions.

39 lead to artificial results due to unnatural hydrophobic interactions.

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

41 diversity of small molecules mainly through hydrophobic interactions.

42 displayed stronger binding due to increased hydrophobic interactions.

43 rming highly stable complexes dependent upon hydrophobic interactions.

44 red spectra, which was ascribed to increased hydrophobic interactions.

45 nteracted with anthocyanins probably through hydrophobic interactions.

46 m Rhodobacter capsulatus (RcFDH) by means of hydrophobic interactions.

47 ssociates between helices E and F of CaM via hydrophobic interactions.

48 ng pocket of AcrB, where they form extensive hydrophobic interactions.

49 of the c-di-GMP molecule, primarily through hydrophobic interactions.

50 e through a combination of electrostatic and hydrophobic interactions.

51 ions are also abolished, suggesting that the hydrophobic interactions alone are insufficient to allow

52 sembly growth is predominantly driven by the hydrophobic interaction along the longer crystallographi

53 S-2- and Mfn-mediated membrane apposition or hydrophobic interactions alter vMIA's ability to organiz

54 of a new network due to hydrogen bonding and hydrophobic interactions among the de-esterified pectin

55 by a detergent-induced redistribution of the hydrophobic interactions among the transmembrane helices

56 s are held together in the pilus filament by hydrophobic interactions among their N-terminal alpha-he

57 e endopeptidases activities using sequential hydrophobic interaction and cation-exchange chromatograp

58 taH of binding comprises both an endothermic hydrophobic interaction and exothermic hydrogen bond com

59 -Ag nano-crystals anchored electrode through hydrophobic interaction and pi-pi electron coupling.

60 lative strength of gold-gold bonding through hydrophobic interaction and silica-silica bonding throug

61 ially attract the metal ions and, afterward, hydrophobic interactions and aromatic ring stacking stab

62 ir populations upon aggregation by promoting hydrophobic interactions and at the same time provide a

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

64 Results indicated both hydrophobic interactions and disulfide bonds were signif

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

66 synthesis is initiated by electrostatic and hydrophobic interactions and formation of self-assembled

67 s by directly binding to Abeta42 species via hydrophobic interactions and hydrogen bonding and remode

68 ppear to preferentially crosslink HMW-GS via hydrophobic interactions and hydrogen bonding, whereas t

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

70 Large flocs, stabilized by hydrophobic interactions and hydrogen bonds, were formed

71 Analysis of hydrophobic interactions and of interhelix hydrogen bond

72 Hydrophobic interactions and shape complementarity enhan

73 of MA-(8-43) to CaM is mediated by numerous hydrophobic interactions and stabilized by favorable ele

74 lloidal phase that seems to be controlled by hydrophobic interactions and surface phenomena.

75 Combining the hydrophobic interactions and the hydrogen-bond-based car

76 M map reveals that SCP binds MCP largely via hydrophobic interactions and the kinked helix of SCP bri

77 analogues of 24 demonstrated that extensive hydrophobic interactions and the unique hydrogen bonding

78 related to its high beta-sheet conformation, hydrophobic interactions and tyrosine crosslinks.

79 imately 20 kJ/mol, suggesting involvement of hydrophobic interactions and/or hydrogen bonds.

80 ing mechanisms, ion pairing, hydrogen bonds, hydrophobic interactions, and conformation effects is de

81 tion of amine groups doubles the strength of hydrophobic interactions, and guanidinium groups elimina

82 ex network consisting of ionic interactions, hydrophobic interactions, and hydrogen binding.

83 ve affinities, in part via electrostatic and hydrophobic interactions, and in part through entropic e

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

85 luding sensitivity to the disruption of weak hydrophobic interactions, and reduced diffusion, increas

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

87 y due to effective charge neutralization and hydrophobic interactions, and/or (iv) additional removal

88 abilized by cation-pi, hydrogen bonding, and hydrophobic interactions; and stabilization of the loop

89 o C4H10, both the size of the cation and its hydrophobic interaction are increased.

90 Hydrophobic interactions are accompanied by hydrogen bon

91 actions conferred by the arginines are lost, hydrophobic interactions are also abolished, suggesting

92 Thus, these hydrophobic interactions are attractive and endothermic

93 Our results further suggest that hydrophobic interactions are dominant in the functional

94 nd pair, while in another pair, Phe50-Phe65, hydrophobic interactions are dominant.

95 Attractive ionic, CH-pi, and hydrophobic interactions are here the major binding forc

96 PfDHODH with three inhibitors suggested that hydrophobic interactions are important for drug binding

97 ophobic properties of sorbates suggests that hydrophobic interactions are of major importance.

98 rogen bonds and pi-pi stacking combined with hydrophobic interactions are responsible for the stabili

99 The hydrophobic interactions are shown to be necessary with

100 s yet rare for artificial receptors, wherein hydrophobic interactions are shown to be responsible for

101 nd dissociation rate constants, we show that hydrophobic interactions are the major driving force in

102 t perturbation, which together indicate that hydrophobic interactions are the major driving force of

103 Ligand self-aggregation does not affect hydrophobic interactions as a main binding factor or the

104 ntrations on nfGNPs-VLPs complexes suggested hydrophobic interactions as the main stabilizing force.

105 e binding involves both hydrogen bonding and hydrophobic interaction, as suggested by negative enthal

106 oration of an aliphatic domain to facilitate hydrophobic interactions, as well as a phenylboronic aci

107 tonavir and demonstrated the leading role of hydrophobic interactions at the sites adjacent to the he

108 perties are not similar, the contribution of hydrophobic interactions becomes more pronounced.

109 A further, hitherto unknown, hydrophobic interaction between CheW and the homologous

110 nteraction is at least, in part, driven by a hydrophobic interaction between the lipids and the hydro

111 cues destabilized F proteins through a local hydrophobic interaction between the N-terminal helix and

112 vate is replaced with a potentially stronger hydrophobic interaction between the phenylalanine and th

113 Structural analysis revealed hydrophobic interaction between the proline's aliphatic

114 interactions were completely lost, although hydrophobic interaction between the side chains of hydro

115 Hydrophobic interaction between this surface and a bound

116 o H-bond involving the 4-OH'' was described, hydrophobic interactions between a tryptophan residue an

117 Mutations that eliminate conserved ionic or hydrophobic interactions between Arg-72 and Asp-122 and

118 This revealed the hydrophobic interactions between aromatic rings of curcu

119 Hydrophobic interactions between atomic-sized hard spher

120 , involving hydrogen bonds, salt bridges, or hydrophobic interactions between conserved residues.

121 nyl specificity arising from pi-aromatic and hydrophobic interactions between crotonyl and aromatic r

122 ow that, in addition to tight intermolecular hydrophobic interactions between CypA and the substrate,

123 Although the mechanism remains unclear, hydrophobic interactions between enzymes and lignin are

124 The hydrophobic interactions between flap and 80 s (80's) lo

125 We conclude that hydrophobic interactions between fluorine and hydrocarbo

126 fect produced on the GQD solution due to the hydrophobic interactions between GO and GQDs.

127 zation of mutant Slo2 channels suggests that hydrophobic interactions between Leu residues in the upp

128 that was stabilized by hydrogen bonds and by hydrophobic interactions between residues 31-35 and resi

129 including a double mutant PS, indicated that hydrophobic interactions between residues of prosegment

130 that the drug is significantly stabilized by hydrophobic interactions between the adamantane and the

131 In addition to hydrophobic interactions between the analyte and carboni

132 mers that assemble to form tetramers through hydrophobic interactions between the faces bearing L17,

133 dwich-like fashion to form tetramers through hydrophobic interactions between the faces bearing V18 a

134 ationship reveals that the electrostatic and hydrophobic interactions between the lipidoids and the p

135 ding by COX-1 but not COX-2, suggesting that hydrophobic interactions between the omega-end of substr

136 rate that cluster formation is controlled by hydrophobic interactions between the peptide backbones,

137 IgG1 Fc homodimer are maintained by multiple hydrophobic interactions between the protein surface and

138 articles) and by the favourable (hydrophobic-hydrophobic) interactions between the nanoparticle and t

139 larly arranged 4-helix bundles stabilized by hydrophobic interactions, but the extent of the overlap

140 The combination of electrostatic and hydrophobic interactions can give rise to complex transl

141 ation at 0 degrees C, which globally weakens hydrophobic interactions, causes gradual and reversible

142 anoparticles (50-150nm) was quantified using hydrophobic interaction chromatography (HIC) and classif

143 Hydrophobic interaction chromatography (HIC) appears to

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

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

146 Conventional hydrophobic interaction chromatography (HIC) provides hi

147 We recently demonstrated that hydrophobic interaction chromatography (HIC) utilizing a

148 ative ion mobility MS (IM-MS) is compared to hydrophobic interaction chromatography (HIC), the refere

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

150 ng inputs from capillary electrophoresis and hydrophobic interaction chromatography to determine the

151 m/methanol extraction in the flow through of hydrophobic interaction chromatography.

152 chromatography, ion-exchange chromatography, hydrophobic-interaction chromatography (HIC), and size e

153 The most significant proved to be the hydrophobic interactions connecting the LA loops of the

154 ted by an extensive and redundant network of hydrophobic interactions, consistent with the high intri

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

156 Thus, disrupting these hydrophobic interactions could be a new therapeutic stra

157 ratio, the larger the alpha, suggesting the hydrophobic interaction determines the attachment of aqu

158 Our results suggest that, by competing for hydrophobic interactions, DMSO can have a small but sign

159 Neither electrostatic nor hydrophobic interactions dominate the adsorption of GG-X

160 ndau-Verwey-Overbeek (DLVO) theory, although hydrophobic interactions dominated MWNTs deposition on a

161 Hydrophobic interactions drive many important biomolecul

162 Extensive hydrophobic interactions established at the Phe-1 site i

163 FA anions cannot dissociate from UCP1 due to hydrophobic interactions established by their hydrophobi

164 dered peptide binds the histone tail through hydrophobic interactions facilitated by nucleosome docki

165 "upright" conformation on mica, whereas the hydrophobic interaction favors the "flat" conformation o

166 Short-range hydrophobic interactions follow, which serve to stabiliz

167 tachment to the unfolded whey protein due to hydrophobic interactions followed by adhesion to the pro

168 PEG works because of multivalent hydrophobic interaction from its repeating methylene uni

169 h the unique geometry from metal complex and hydrophobic interactions from simple peptides, we demons

170 The hydrophobic interactions from the inhibitor is aimed to

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

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

173 , but the influence of this heterogeneity on hydrophobic interactions has not been tested experimenta

174 tes thus formed via electrostatic as well as hydrophobic interactions have been explored for the sens

175 Aromatic-aromatic and aromatic-hydrophobic interactions have been proposed to play a ro

176 (GE) from Alcalase 2.4 L was purified using hydrophobic interaction (HIC) and ion-exchange (IEX) chr

177 Peptide binding is enhanced by hydrophobic interactions; however, poor solubility promo

178 rucial enzyme/inhibitor interactions such as hydrophobic interactions, hydrogen bonding, and heme iro

179 d compounds, suggesting that, in addition to hydrophobic interactions, hydrogen-bonding is predominan

180 o be hydrophilic in nature compared with the hydrophobic interaction in E. coli.

181 two hydrogen-bonded dimers that pack through hydrophobic interactions in a sandwich-like fashion.

182 and guanidinium groups eliminate measurable hydrophobic interactions in all pH ranges investigated.

183 The roles of divalent metal and hydrophobic interactions in controlling packaging-trigge

184 Here we evaluate the role of hydrophobic interactions in enzyme-lignin binding.

185 Mapping surface hydrophobic interactions in proteins is key to understan

186 ast decade has improved our understanding of hydrophobic interactions in simple model systems, but mo

187 c chain snakes along a shallow cavity making hydrophobic interactions in the "switch region", as well

188 Hydrophobic interactions in the cavity sustain the fusio

189 ur study reveals the critical role played by hydrophobic interactions in the formation of this virus-

190 its hydrophobic counterpart is stabilized by hydrophobic interactions in the membrane.

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

192 ctions, our results reveal the importance of hydrophobic interactions in the same interfaces.

193 the alpha5 helix of Galphai1, especially the hydrophobic interactions in this region, plays a key rol

194 inding pocket can thus determine whether the hydrophobic interactions in which it engages are enthalp

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

196 and that their assembly is promoted by weak hydrophobic interactions, indicative of a liquid crystal

197 e ERCC1 point mutation F231L, located at the hydrophobic interaction interface of ERCC1 (excision rep

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

199 omplete description of the forces underlying hydrophobic interactions is lacking.

200 ons, suggesting that the capacity to disrupt hydrophobic interactions is responsible for the effect o

201 rol further interacts with 11-MUA-Au NDs via hydrophobic interactions, leading to inhibition of O2 qu

202 hes, we show that this mutant loses critical hydrophobic interactions, leading to significant rearran

203 e double mutation in Act variant weakens the hydrophobic interactions, leading to the transition from

204 ultraperformance liquid chromatography and a hydrophobic interaction liquid chromatography column cou

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

206 ther levels including the hydrophobic effect/hydrophobic interactions, mechanisms of protein folding

207 Hydrophobic interaction membrane chromatography, which w

208 tabilized in aqueous solution by intraligand hydrophobic interactions mimicking the macrolide structu

209 n which Phe(151) is the central residue in a hydrophobic interaction network connecting the active si

210 drogen bonding during pressurisation and not hydrophobic interactions nor disulphide cross-links.

211 y of TREA hybrids appears to be dominated by hydrophobic interactions, not base pairing of the DNA ar

212 at support the hypothesis that a stabilizing hydrophobic interaction occurs with 1a.

213 to the linking position of L-fucose, and the hydrophobic interaction of L-fucose with the beta-face o

214 glutamic acid-lysine pairs, in concert with hydrophobic interactions of core residues, provide the m

215 brane thickness but could be rationalized by hydrophobic interactions of lysines at the bilayer inter

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

217 ween Phe(81) and Phe(129) along with several hydrophobic interactions of Phe(81), which are not seen

218 her the optimization of hydrogen bonding and hydrophobic interactions of second-generation novologues

219 otently to both the DDR and ABL kinases, the hydrophobic interactions of the ABL P-loop appear poorly

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

221 Hydrophobic interactions of the methyl group rather than

222 protein hisactophilin reveal that nonnative hydrophobic interactions of the myristoyl with the prote

223 The stacking occurs also due to hydrophobic interactions of the rings of both molecules.

224 to find that EXLX1 binds the ligands through hydrophobic interactions of three linearly arranged arom

225 In addition, we take advantage of hydrophobic interactions of transmembrane helices to man

226 We also find 10 important hydrophobic interactions, of which 4 interactions are in

227 shows that the effects of electrostatic and hydrophobic interactions on the translocating potential

228 he chimeras were immobilized via nonspecific hydrophobic interactions onto glass planar waveguides mo

229 adsorption employ electrostatic attraction, hydrophobic interaction, or pi-pi stacking, none of whic

230 he interface is characterized by substantial hydrophobic interactions overlapping the binding surface

231 olesterol sensing, with hydrogen bonding and hydrophobic interactions participating in cholesterol lo

232 anionic exchange (Q-Sepharose, pH 7.5), and hydrophobic interaction (phenyl-Sepharose) chromatograph

233 nal studies revealed the important role that hydrophobic interactions play in the aqueous assembly of

234 Two critical residues, involved in a hydrophobic interaction, provide a ligand-binding platfo

235 ongly to the CH3-terminated SAM surfaces via hydrophobic interactions (range of adhesive interaction

236 Results showed that CETP binds to HDL via hydrophobic interactions rather than protein-protein int

237 ns involve 20 hydrogen bonds and a number of hydrophobic interactions resulting in an extended buried

238 000/water nanoemulsions because of favorable hydrophobic interactions; second, the nanoemulsions had

239 ine 215 as a key residue within a network of hydrophobic interactions stabilizing the entire BAR dime

240 at reveal a dramatic change in the surfaces' hydrophobic interaction strengths on co-immobilization o

241 benzene, a compound known to interfere with hydrophobic interactions, such as those between pairing

242 lution or in cells, and we propose that this hydrophobic interaction surface may mediate binding to a

243 ds MIF mainly on the protein surface through hydrophobic interactions that are stabilized by hydrogen

244 In contrast, the EC1/EC4 interface comprises hydrophobic interactions that provide non-selective dime

245 molecular fragments or surfaces mediates the hydrophobic interactions that underlie a broad range of

246 As partitioning is often driven by hydrophobic interactions the uptake of amino acids and p

247 ally, we show that as compared with a purely hydrophobic interaction, the Met-aromatic motif yields a

248 reas the adamantane site binds CB solely via hydrophobic interactions, the CB unit at the butyl site

249 fect of dissolved gas and its connection to 'hydrophobic' interactions, the problem of water at diffe

250 itochondria that binds incoming proteins via hydrophobic interactions thereby mediating protein trans

251 Inspired by protein folding, we introduce hydrophobic interactions to expand the assembly language

252 ted against a second layer of dimers through hydrophobic interactions to form a fibril-like assembly

253 and cooperates with nearby arginines and the hydrophobic interactions to provide the binding specific

254 ometry revealed that LL-37 binds by specific hydrophobic interactions to the His-40-Lys-50 segment of

255 tBid (p15), that are held together by strong hydrophobic interactions until the complex binds to memb

256 that TAP/TPN complex formation is driven by hydrophobic interactions via leucine zipper-like motifs.

257 ents between intrareceptor electrostatic and hydrophobic interactions, we enabled complementary guest

258 Hydrophobic interactions were evaluated through the addi

259 Hydrophobic interactions were found to be relatively les

260 ized to be due to increased particle-surface hydrophobic interactions (when compared to silica surfac

261 selectivity for guanine estimation is due to hydrophobic interactions, which are assisted by the low

262 We also found that hydrophobic interactions, which could lead to a mixed-mo

263 ydrogenase complex appears to be involved in hydrophobic interactions, which may limit its exposition

264 variations related to the hydrogen bonds and hydrophobic interactions, which occur with the formation

265 ratrol-gliadin binding mainly occurs through hydrophobic interactions while the binding with zein is

266 In contrast, nonspecific hydrophobic interactions, while hardly affecting the enc

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

268 sed molecular rigidity of the dye due to its hydrophobic interaction with protein lead to fluorescenc

269 due in the drug-binding pocket would disrupt hydrophobic interaction with tariquidar and inhibit its

270 37)LAGLF(442) helix of the E2 protein in the hydrophobic interaction with the D-helix of CD81, thereb

271 es, whereas its extended xylose moiety forms hydrophobic interactions with a Tyr residue.

272 ts away from the heme group and has multiple hydrophobic interactions with aliphatic amino acid resid

273 were also explored to enhance pi-pi stacking/hydrophobic interactions with amino acids of Abeta42.

274 ace coming from the various electrostatic or hydrophobic interactions with biomolecules.

275 ler valine side chain in PR(I50V) eliminated hydrophobic interactions with inhibitor and the other su

276 flet, establishing extensive hydrophilic and hydrophobic interactions with MsbA.

277 mechanisms include charge neutralization and hydrophobic interactions with natural organic matter rem

278 (at the end of the heme channel) and several hydrophobic interactions with other residues and the hem

279 Ac form several hydrogen bonds and extensive hydrophobic interactions with protein atoms, indicating

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

281 whereas affinity is increased by nonspecific hydrophobic interactions with the anomeric substituent.

282 that perturbing the Phe-336 residue disturbs hydrophobic interactions with the beta2-beta3 strands an

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

284 pairs and can be rationalized from increased hydrophobic interactions with the FimH hydrophobic ridge

285 an alpha-helical conformation and engages in hydrophobic interactions with the HA very similar to tho

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

287 n to the negatively charged cell surface and hydrophobic interactions with the membrane lipids enable

288 budding are defective in the absence of key hydrophobic interactions with the membrane.

289 ificity for methylcytosine depends on direct hydrophobic interactions with the methylcytosine 5-methy

290 ture shows that cholesterol is stabilized by hydrophobic interactions with the TM helix and polar and

291 ange of hydrophobicity as a measure of their hydrophobic interactions with the transport barriers.

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

293 ily by five aromatic residues that also make hydrophobic interactions with the xylose side chains of

294 ange of hydrogen bonding, salt bridging, and hydrophobic interactions with thrombin to achieve tight

295 enthalpy-driven interactions, in addition to hydrophobic interactions, with the formation of complexe

296 Hydrophobic interactions within a lipophilic pocket past

297 interactions between neighboring strands and hydrophobic interactions within each strand.

298 pecifically this may be due to disruption of hydrophobic interactions within individual zein proteins

299 hogenic amyloid fibrils, FUS-LC fibrils lack hydrophobic interactions within the core and are not pol

300 a set of highly conserved electrostatic and hydrophobic interactions working harmoniously to regulat