ライフサイエンスコーパス: electrostatic

1 ntrolled mean-field treatment of long-ranged electrostatics.

2 eolipid solvation energy and bilayer surface electrostatics.

3 te is required to explain its sensitivity to electrostatics.

4 -HASEL (hydraulically amplified self-healing electrostatic) actuator as a model system.

5 val can be successfully achieved based on an electrostatic adsorption mechanism.

6 The combination of electrostatic adsorption of exenatide to the membrane su

7 With the help of an electrostatics-aided covalent self-assembly approach, we

8 3DI instrument is composed of a miniaturized electrostatic analyzer (ESA) and a deflector, backed by

9 ant and ancestor forms revealed increases in electrostatic and aromatic interactions between distinct

10 f the actuated nano-manipulator subjected to electrostatic and Casimir attractions are investigated.

11 we show that myosins in STFs mirror the more electrostatic and cooperative interactions that underlie

12 We investigate roles of electrostatic and entropic interactions driving selectiv

13 eties, PCET is driven by complex interfacial electrostatic and field gradients that are difficult to

14 self-sensing artificial muscles that couple electrostatic and hydraulic forces to achieve diverse mo

15 Further, we show that the evaluation of electrostatic and hydrophobic characters of the mabs is

16 resveratrol to the CpLIP2 catalytic site via electrostatic and hydrophobic forces.

17 attachment of the peptide with the WS(2) via electrostatic and hydrophobic interactions results in fl

18 Our data support that 4E10 establishes electrostatic and hydrophobic interactions with the vira

19 ith the PS nucleic acid through a network of electrostatic and hydrophobic interactions, which provid

20 tone proteins, histone tails, intrachromatin electrostatic, and other interactions decide the nature

21 systems were exposed to HA, osmotic-steric, electrostatic, and van der Waals forces dominate.

22 Using an analogy with electrostatics, and building on recent developments in a

23 on of noncanonical Phe analogs with distinct electrostatics at two positions.

24 de-to-side 2D assemblies and shows that both electrostatic (at the nanoscale) and thermal (in bulk) s

25 Electrostatic attraction facilitates heteroaggregation a

26 EDLs, it is solely based on the macroscopic electrostatic attraction of electrolytes for the charged

27 urface positive electric field that exhibits electrostatic attraction to the negative [UO(2) (CO(3) )

28 cationic LAE (CNCs/LAE) were formed through electrostatic attraction which were characterized using

29 polymer beads cannot only adsorb Cr (VI) via electrostatic attractions but also reduce it to Cr (III)

30 We further employ a simple electrostatics-based model to show that this slope can e

31 ectively compacts plasmid DNA (pDNA) through electrostatic binding and intercalation.

32 Our findings provide new insights into how electrostatics can be employed to tune the catalytic act

33 cient with respect to the force capacity per electrostatic capacitive energy and are robust to defect

34 ork suggests a possible strategy for scaling electrostatic catalysis by applying a pulsed external fi

35 thus overcoming a central limitation of the electrostatic catalysis paradigm.

36 can control this charge transfer and impart electrostatic catalysis.

37 sponse of its dipole moment to environmental electrostatic changes.

38 0.6-0.7 and possess both charge transfer and electrostatic characteristics.

39 e) (PABA) does not only provide the suitable electrostatic charge and non-denaturing environment for

40 dity to host cellular receptors, mediated by electrostatic charge interactions with negatively charge

41 ts of metal coordination, and the associated electrostatic charge patterns, on the complex structural

42 this discrepancy and thus further associate electrostatic charge with immune escape and viral evolut

43 jugation site, surrounding residue's pI, and electrostatic charge, may directly impact the drug relea

44 ectroscopy reveals a fundamentally different electrostatic color tuning mechanism for the neutral sta

45 nteractions with model peptides that exploit electrostatic complementarity and define a novel amyloid

46 otential (ESP) surfaces in order to optimize electrostatic complementarity is a key activity in drug

47 zinc-insulin hexamers, further stabilized by electrostatic complex formation with chitosan polymer.

48 ing bile acid-based prodrugs, bile acid/drug electrostatic complexation and bile acid-containing nano

49 Electrostatic complexes formed from 0.02% CNCs and 0.1%

50 -induced bolstering of the B-state Tpm-actin electrostatic contacts and an increased Tpm troponin T1

51 on highly-favorable, conformation-dependent electrostatic contacts between actin and tropomyosin, wh

52 sient nonspecific hydrophobic and long-range electrostatic contacts form between ArkA and the binding

53 and R147, forms numerous, highly favourable electrostatic contacts with Tm that are critical for est

54 lanol-rich surface of silica is dominated by electrostatic contributions and a spectrum of several pe

55 Finally, this electrostatic control explains how protein crowding is s

56 Here, we demonstrate unprecedented electrostatic control of dual-gated Gaussian heterojunct

57 Direct demonstration of electrostatic control of the superlattice bands over a w

58 airgap while the device moves, for improved electrostatic control.

59 gy binding an electron-hole pair through the electrostatic Coulomb force-independent of its electroni

60 protons by tightly linked conformational and electrostatic coupling principles.

61 ed on the tip of the needle electrodes by an electrostatic deposition method.

62 Earlier investigations identified dominant electrostatic dipolar interactions, while others implica

63 h short-range inductive polarisation augment electrostatic dipolar interactions.

64 Electrostatic doping is not the only route to charging l

65 tically addressable single spins by means of electrostatic doping the localized excitons.

66 the Fermi level into these flat bands using electrostatic doping, we observe a pseudogap-like deplet

67 ir indoor microbial flora through the use of electrostatic dust collectors (EDCs).

68 metal ions have a long-range (~10 angstrom) electrostatic effect on restructuring water network in t

69 Electrostatic effects are probed by using zwitterionic p

70 rostatics quantitatively and demonstrate how electrostatic effects bias the pathway of chromophore ph

71 our results indicate that hydrophobic and/or electrostatic effects in the cavity are strongly destabi

72 Electrostatic effects on a range of 2-phenyl-5-methyltet

73 Competing roles for steric and electrostatic effects that govern bond-specific photoiso

74 bstituents: hyperconjugative, resonance, and electrostatic effects.

75 orbital analysis, including natural Coulomb electrostatics, elucidates the presence of three influen

76 ion: an intrinsic rectification caused by an electrostatic energy barrier from positively charged ami

77 h tetrahedral sites results in high positive electrostatic energy barriers within the interlayer, cre

78 values to aluminosilicate minerals with high electrostatic energy barriers.

79 insights into how the elastic energy and the electrostatic energy determine the extent of segregation

80 exibility and distorts the actin-tropomyosin electrostatic energy landscape that, in muscle, result i

81 tion of oxygen vacancies that couples to the electrostatic energy of the dopant in the perovskite lat

82 in the presence of polarization effects, the electrostatic energy stored in the double-layer structur

83 erial energetics are tuned through molecular electrostatic engineering and mesoscale structural contr

84 To address this, we outline an electrostatics-enhanced covalent self-assembly strategy

85 in low dielectric solvents to non-isotropic electrostatic enhancements in the key ion pair intermedi

86 this unique feature to further modulate the electrostatic environment around the Fe-oxido unit.

87 tation of the solvent molecules modifies the electrostatic environment around the Menshutkin species

88 s simulations suggest that modulation of the electrostatic environment due to protein conformational

89 cise tailoring of inhibitors to the enzyme's electrostatic environment.

90 environment and a generalization of Donnan (electrostatic) equilibrium that accounts for active ion

91 t of ER agonists showed that both steric and electrostatic factors contributed to the functional defi

92 What is particularly striking is that electrostatic field effects upon key photochemical trans

93 However, the nature of the electrostatic field generated by the (remote) charged so

94 ; we then demonstrate that oriented internal electrostatic fields arising from remote charged functio

95 Oriented electrostatic fields can exert catalytic effects upon bo

96 ullvalene can be affected by the presence of electrostatic fields.

97 nts in the agreement between CG and all-atom electrostatic fields.

98 ch in turn generates non-destructive, strong electrostatic fields.

99 The electrostatic force between the negatively charged siali

100 measure a nonlinear polarization through its electrostatic force is a powerful means to revisit nonli

101 Here, by using electrostatic force microscopy, this effect is observed

102 lly and spatially resolving the microscopic, electrostatic forces arising from a nonlinear optical po

103 , capillary pressure may overwhelm repulsive electrostatic forces, assembling aggregates that are out

104 ntrolled using non-thermal stimuli including electrostatic gating and photoexcitation.

105 y chemical doping, interface modulation, and electrostatic gating, there is as of yet no analogue of

106 ILs from constituting an ideal platform for electrostatic gating.

107 m for encoding cysteine redox sensitivity by electrostatic gating.

108 Overall, we suggest electrostatics-guiding DNA to a specific protein binding

109 ment of hydraulically amplified self-healing electrostatic (HASEL) actuators, a new class of high-per

110 These electrostatic hydrogels have a high affinity for a wide

111 onformational properties owing to additional electrostatic, hydrogen-bonding, and steric interactions

112 theory (CDFT)-of the relative importance of electrostatic, i.e., "hard-hard", versus spin-pairing, i

113 ty, low doping in the channel, and excellent electrostatic integrity, receive very limited benefit fr

114 We identify a pH-sensitive electrostatic interaction between positively charged arg

115 ctrostatic term depends on the change in the electrostatic interaction between the charges on each en

116 y, we show the Tafel slope to arise from the electrostatic interaction between the dipole of *CO[Form

117 Electrostatic interaction between the fluorophores and t

118 Over days, the electrostatic interaction between two monomers induces a

119 Hydrogen bonding in addition to electrostatic interaction contribute to stability of pec

120 onment, adopting a strategy of enhancing the electrostatic interaction in hydrophobic media at high t

121 CQDs into AuNPs, gets them aggregated due to electrostatic interaction resulting in quenching the FL

122 forms toroidal homopolymers, the additional electrostatic interaction that can also guide rosette as

123 the PscD residues predicted to mediate this electrostatic interaction using a two-hybrid analysis.

124 Our results reveal a juxtaposed bipartite electrostatic interaction utilized by the nucleosome to

125 inhibit CATH-2 function, showing a stronger electrostatic interaction with the peptide than other li

126 i slurry (CSi, CSi-Mg6, or CSi-Mg10) through electrostatic interaction.

127 four hydrophobic pockets P1-P4 and one major electrostatic interaction.

128 b by providing optimal physical trapping and electrostatic interaction.

129 , development, and exploitation of molecular electrostatic interaction.

130 Modeling of the density maps reveals how electrostatic interactions and a mobile loop participate

131 zation, the applied potential governed these electrostatic interactions and electrochemical reactions

132 w more diverse paths characterized by weaker electrostatic interactions and more than 10 times shorte

133 d well-folded PTP domain through multivalent electrostatic interactions and regulated by an intrinsic

134 g the context dependency of the dominance of electrostatic interactions and the occurrence of n->pai*

135 erties of a water model whose intermolecular electrostatic interactions are entirely short-ranged are

136 Protein-protein electrostatic interactions are modulated by relative per

137 drives Gag onto the plasma membrane through electrostatic interactions at its highly-basic-region (H

138 translocation is facilitated by a series of electrostatic interactions between a cation and key char

139 R domains act as specificity factors through electrostatic interactions between a pair of polar resid

140 Results indicated that electrostatic interactions between bacteria and ionic el

141 nt KRAS-RBD interaction results in transient electrostatic interactions between KRAS and CRD, and we

142 e simulations show that both hydrophobic and electrostatic interactions between monomers help maintai

143 are key to initial JDP/Hsp70 recognition-via electrostatic interactions between oppositely charged su

144 Direct electrostatic interactions between polar and charged ami

145 ffusion processes are mediated by long-range electrostatic interactions between positively charged pr

146 Dimerization of KRAS-GTP, stabilized by electrostatic interactions between R135 and E168, favors

147 ad a prearranged catalytic site, with strong electrostatic interactions between the active-site resid

148 Favorable electrostatic interactions between the dienophile and th

149 mulations confirm the existence of favorable electrostatic interactions between the high charge-densi

150 s, that this is due to the strong attractive electrostatic interactions between the nascent chain and

151 lling of the polymeric matrix and weaken the electrostatic interactions between the negatively charge

152 Importantly, the electrostatic interactions between the Zn(2+) and the ho

153 We find that screened electrostatic interactions can drive the formation of co

154 rbital overlaps but from weak dispersion and electrostatic interactions combined with stereochemical

155 composition of cellular systems renders the electrostatic interactions different from those in physi

156 Here we reveal the importance of electrostatic interactions for the activity of INPs from

157 Coulombic electrostatic interactions have been shown to contribute

158 tational approach confirmed the dominance of electrostatic interactions in a new series of synthetic

159 d intermolecular hydrogen bonding as well as electrostatic interactions in the antiparallel stacking

160 r the cis isomer is also driven by repulsive electrostatic interactions in the case of a syn-facial h

161 of the interacting region and intrachromatin electrostatic interactions influence the packing density

162 tion of ASIC1a is primarily mediated through electrostatic interactions of basic amino acids in the B

163 demonstrated the role of sequence-dependent electrostatic interactions of peptoids with the DNA back

164 These data show that H-bonding and electrostatic interactions of the base within the MutY a

165 DIs compared to the charged PDIs, reflecting electrostatic interactions of the latter with oppositely

166 We found that electrostatic interactions play a central role in protei

167 omposition analyses suggest that orbital and electrostatic interactions play a major role in altering

168 Electrostatic interactions play a pivotal role in enzyma

169 We conclude that electrostatic interactions play an essential role in the

170 We further describe how BIN1's electrostatic interactions regulate membrane bending: th

171 els of short-range dispersive and long-range electrostatic interactions respond to airborne contamina

172 These results show that H-bonding and electrostatic interactions taking place in the aqueous p

173 und to Rubisco reveals a series of conserved electrostatic interactions that are only made with prope

174 ctivators use nonspecific hydrophobic and/or electrostatic interactions to bind to coactivators, with

175 s that utilize long-range binding effects of electrostatic interactions to bind with the intra-NP neg

176 can exploit their confinement and favorable electrostatic interactions to finely control nucleotide

177 ighlighting the destabilizing role played by electrostatic interactions vis-a-vis quaternary structur

178 levels of RNA promote condensates formed by electrostatic interactions whereas relatively high level

179 J- to an H-aggregation was induced by strong electrostatic interactions with amine-terminated polysty

180 ding of 2-OH-NQ to ThyX is also explained by electrostatic interactions with Arg199.

181 actions with Trp(291) of the S1' subsite and electrostatic interactions with Asp(125) of the S2' subs

182 cting proteins, it is due to their repulsive electrostatic interactions with the exit tunnel.

183 onto the QDs is driven by multicoordinating electrostatic interactions with the ion-rich surfaces of

184 trate that species (namely K(+)) with strong electrostatic interactions with the oxygen functionaliti

185 ition state stabilization through H-bond and electrostatic interactions with the positively charged R

186 Here we apply drug carriers that leverage electrostatic interactions with the tissue's high negati

187 hat establishment of peripheral, nonspecific electrostatic interactions with the viral membrane throu

188 and Lys(328), are predicted to form critical electrostatic interactions with tropomyosin (Tpm) that p

189 N1 of uronic isofagomine (2) made strong electrostatic interactions with two catalytic glutamates

190 ue to preferential hydrophobic partitioning, electrostatic interactions, and diffusion into lower-per

191 greatly between proteins due to differential electrostatic interactions, can influence ribosome recyc

192 ns follow a path involving strong non-native electrostatic interactions, resulting in a transition ti

193 Probing the role of surface structure in electrostatic interactions, we report the first observat

194 ightly bound ion estimations of ion-mediated electrostatic interactions.

195 l as other physiological processes driven by electrostatic interactions.

196 potentials (and/or partial charges) for the electrostatic interactions.

197 achievable using typically less directional electrostatic interactions.

198 is acid/base hardness, steric hindrance, and electrostatic interactions.

199 f hydrogen bonding, metal-metal bonding, and electrostatic interactions.

200 es were formed instantaneously mostly due to electrostatic interactions.

201 ctions, such as hydrogen bonds (H-bonds) and electrostatic interactions; however, there is little qua

202 a compact auto-inhibited state stabilized by electrostatic intramolecular interactions between the in

203 y forces and torques due to a combination of electrostatic ion-solvent correlations and dipolar inter

204 ains with different orientations generate an electrostatic landscape with an interfacial energy offse

205 ew technological capabilities such as stable electrostatic levitation.

206 The cylinder is usually placed inside an electrostatic linear ion trap so that the ions oscillate

207 (n), consisting of cyanostar-stabilized anti-electrostatic linkages, shows adhesion strength comparab

208 raditional viscosifier, organoclay, that has electrostatic linkages.

209 )-OH) with magnetic nanoparticles (MNPs) and electrostatic loading of chloroperoxidase (CPO).

210 pK(a) 's upon ET at copper, allowing SOD1's "electrostatic loop" to attract superoxide with equal aff

211 Furthermore, electrostatics may rescue the heparin/protein interactio

212 rgets hinder phagocytosis by both steric and electrostatic means.

213 surrounded by basic residues, suggesting an electrostatic mechanism for HS binding.

214 The electrostatic nature of the effect enabled the selective

215 These ESP surfaces need to reflect the true electrostatic nature of the molecules, which typically m

216 Most notably, SS-31 modulated the surface electrostatics of both model and mitochondrial membranes

217 that, by altering the morphology and surface electrostatics of the outer leaflet, the insertion of AC

218 urface, which is likely to alter the surface electrostatics of the outer leaflet.

219 cceptor distance and geometry as well as the electrostatics of the reactants.

220 e found to spontaneously associate into anti-electrostatic oligomers via hydrogen bonding interaction

221 ize and oligomerize by overcoming long-range electrostatic opposition.

222 erogeneous transient interactions, including electrostatic pairings, and an increased disorder for th

223 architectures differences in size, shape and electrostatic parameters between isoforms.

224 Molecular dynamics (MD) simulations and electrostatic potential (ESP) charge calculations were c

225 Inspecting protein and ligand electrostatic potential (ESP) surfaces in order to optim

226 Surprisingly, the electrostatic potential across the adsorbed polyelectrol

227 Throughout the NPC, we find a polarized electrostatic potential and a diffuse thermoreversible F

228 ion, cumulant terms of all odd orders in the electrostatic potential are removed.

229 Changes in the electrostatic potential are then tracked via Stark shift

230 thods, showing that the mutation changes the electrostatic potential at the active site and reduces t

231 robe of the heterogeneity of the interfacial electrostatic potential at the alpha-Al(2)O(3)(0001)/H(2

232 riginating from octahedral sites produce low electrostatic potential barriers within the interlayer,

233 orming docking simulation, following surface-electrostatic potential estimation in the predicted area

234 w include 13 shape features and minor groove electrostatic potential for standard DNA and four shape

235 he dimer interface that create an attractive electrostatic potential funneling the zinc cations towar

236 t work also identified other factors such as electrostatic potential in the vicinity of the active si

237 atalytic activity by increasing the positive electrostatic potential in the vicinity of the conserved

238 icate structure and the resultant changes in electrostatic potential influence the sorption of organi

239 e of interaction closely correlates with its electrostatic potential map.

240 The application of atomistic electrostatic potential mapping of both sorbent and sorb

241 Analysis using electrostatic potential maps highlights that this differ

242 uch anion selectivity arises from a positive electrostatic potential of the central lumen rendered by

243 The changes modified the electrostatic potential of the RRM leading to a greater

244 ts of a monotonic dependence of the built-in electrostatic potential on depth and continuity of the p

245 nts that could not be described by the basic electrostatic potential theory or by assuming that sorba

246 omplemented with theoretical analysis of the electrostatic potential to establish how and why protons

247 ue-residue interaction schemes with a shared electrostatic potential.

248 frontier) orbital interactions and molecular electrostatic potentials (and/or partial charges) for th

249 enerates a surface with intensified positive electrostatic potentials (PEP) for RNA binding and dimer

250 ein, the spatially inhomogeneous interfacial electrostatic potentials and electric fields of GCC orga

251 structure of the surface and the interfacial electrostatic potentials and fields that govern PCET the

252 dictors of reaction kinetics than calculated electrostatic potentials, suggesting utility in other co

253 te catalysis and provides a template for how electrostatic preorganization can be measured in enzymat

254 inted microfiber constructs using near-field electrostatic printing (NFEP) and graphene oxide (GO) co

255 For that, we solve the electrostatic problem of a conducting hyperboloid with a

256 chemistry affecting surface complexation and electrostatic processes.

257 plays a flattened chair conformation and the electrostatic profile of this compound reveals a large d

258 The electrostatic properties across the S1 pocket are furthe

259 narily conserved in CLC channels where their electrostatic properties and conformational flexibility

260 ar S1 pockets, our results suggest different electrostatic properties of Asp189 possibly contributing

261 lar imaging of the chemical, electronic, and electrostatic properties of single molecules, but also t

262 We systematically altered the electrostatic properties of the green fluorescent protei

263 ations, remarkably little is known about the electrostatic properties of the individual organellar me

264 nt SWING filters show exceptional long-range electrostatic property driven by aeolian vibration, enab

265 The work employing the transmembrane-electrostatic proton localization theory reported here h

266 mbines the principles of micro-discharge and electrostatic pulling, without the need of any power-con

267 we evaluate the contributions of sterics and electrostatics quantitatively and demonstrate how electr

268 It has several advantages over conventional electrostatic relays, including low actuation voltages w

269 y a steric hindrance mechanism, coupled with electrostatic repulsion and entrance effects.

270 in experiments, but it rotates because of an electrostatic repulsion and forms a hydrophobic interfac

271 electron microscopy, most likely due to the electrostatic repulsion between 4-ABA-grafted graphene l

272 self-limiting nanoparticle bonding, whereas electrostatic repulsion between colloidal bonds governs

273 pose that the E46K misfolding pathway avoids electrostatic repulsion between K46 and K80, a residue p

274 in the case of the longer chains due to the electrostatic repulsion between the low-pI ACE2 and the

275 Added electrostatic repulsion between the membrane surfaces is

276 Based on Coulomb's Law alone, electrostatic repulsion between two anions is expected t

277 tors stabilizes the open conformation as the electrostatic repulsion due to the reaped electrons push

278 pressed thylakoid membranes due to increased electrostatic repulsion of adjacent membranes; 2) p-PSBS

279 bilayer structure due to the adsorption and electrostatic repulsion of chaotropes on the hydrophobic

280 OH generation from neutral H(2)O(2) and that electrostatic repulsion of contaminants from the electro

281 uir kinetic model accounting for an enhanced electrostatic repulsion originating from the surface imm

282 expected to be close to each other, causing electrostatic repulsion.

283 o hydrogen bond formation, which outcompeted electrostatic repulsion.

284 propose that the NTD structure serves as an electrostatic scaffold to recognize the shape of an RNA

285 of other materials on the nanoscale by using electrostatic scanning probe techniques.

286 on donor-acceptor interactions increased the electrostatic screening of the exciton, in turn lowering

287 Electrostatic self-interaction of the polarization charg

288 nanofibre-based film, produced by a scalable electrostatic spinning process, enables selective mid-in

289 polymerase, with Arg517 and Asn513 providing electrostatic stabilization of G-T*.

290 ron porphyrin ORR catalysts, we suggest that electrostatic stabilizers of O(2)-bound intermediates ar

291 hamber possesses a strikingly large negative electrostatic surface potential, adding additional "func

292 tuent, such as the Hammett sigma-constant or electrostatic surface potential.

293 s in the substrate channels (in shape, size, electrostatic surface, and residue composition) lead to

294 This electrostatic term depends on the change in the electros

295 f an additional positive, distance-dependent electrostatic term in the PCET driving force, which atte

296 chromophore can be more sensitive to protein electrostatics than can the anionic counterpart.

297 excited molecular ions with merged beam and electrostatic trap experiments.

298 s, the simultaneous achievement of efficient electrostatics, very small sub-thermionic subthreshold s

299 on efficiency, minimum output impedance, and electrostatic voltage applicability.

300 We suggest that an electrostatic wave propagates in forward and reverse dir