ライフサイエンスコーパス: electrostatic field

1 eld and the remainder of the variance to the electrostatic field.

2 films on gold in the presence of an applied electrostatic field.

3 ng that these residues interact with the RNA electrostatic field.

4 at the nucleosome retains a strong, negative electrostatic field.

5 d the polar wind) suggest the presence of an electrostatic field.

6 of polymeric and ceramic materials using an electrostatic field.

7 ome nevertheless maintains a strong negative electrostatic field.

8 ge by conducting Stokes experiments under an electrostatic field.

9 e energetic consequences of the nucleic acid electrostatic field.

10 the diffusion of ions in the presence of an electrostatic field.

11 rature and decreasing pH, despite the higher electrostatic field.

12 curs in water, which itself exerts a sizable electrostatic field.

13 calibrates their vibrational frequencies to electrostatic field.

14 d to quantify perturbations to the protein's electrostatic field.

15 of proteins are on average aligned with the electrostatic field.

16 and the opposite face has a strong positive electrostatic field.

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

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

19 vity with observed differences in steric and electrostatic fields.

20 ngle reaction can be accelerated by distinct electrostatic fields.

21 ned by carefully-engineered local strain and electrostatic fields.

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

23 from artificially created electromagnetic or electrostatic fields.

24 lerated via strong charge-separation-induced electrostatic fields.

25 bitrap in that ions are trapped using solely electrostatic fields.

26 ure by a mechanism that does not involve the electrostatic field across the bilayer, but rather elect

27 ange electrostatic interactions, whereby the electrostatic field acts as a 'funnel' that sweeps the G

28 he phenolate of Tyr 149 opposes the positive electrostatic field and attenuates the reactivity of NAD

29 as nitriles, are linearly sensitive to local electrostatic field and can serve as a molecular electri

30 nto one cage (1) leads to magnified positive electrostatic field and electron-accepting strength in f

31 Analyses of these distributions of electrostatic field and internal dynamics, together with

32 re waters is sufficient to reshape the local electrostatic field and modulate the energetics of condu

33 The difference may be due to both the larger electrostatic field and the greater asymmetry of the cha

34 binding site, which lies 80% into the pore's electrostatic field and thus exhibits a marked voltage d

35 recise manipulation of chemical reactions by electrostatic fields and opens up a universal route to d

36 ng correlation between the calculated steric-electrostatic fields and the observed biological activit

37 of the built-in electric field, the applied electrostatic field, and charged impurities or adsorbate

38 rmeation rate is sensitive to the inner pore electrostatic field, and they are consistent with creati

39 comparison reveals that the CoMFA steric and electrostatic fields are compatible with stereochemical

40 We show how electrostatic fields are sensitive in defective areas to

41 icance of the CoMFA models; thus, steric and electrostatic fields are the relevant descriptors for th

42 oretical modelling reveal that the polarized electrostatic field arising from the cationic groups sup

43 finite size of the cavity and the favorable electrostatic field arising from the pore helices.

44 e channel axis due to the strong transversal electrostatic field arising from those residues.

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

46 s are primarily a response to changes in the electrostatic field around the heme (a transient Stark s

47 ith a high-speed 2D electron detector to map electrostatic fields around individual atoms in 2D monol

48 Electrostatic field assistance is applied to improve NP

49 This electrostatic field-assisted carrier separation and perc

50 tity of supporting electrolyte to screen the electrostatic field associated with MEH+.

51 data gives an estimate of the average total electrostatic field at this location.

52 To quantitatively assess the landscape of electrostatic fields at discrete locations and orientati

53 y wave-particle interactions(4) and a global electrostatic field between the ionosphere and space (ca

54 Electrostatic field calculations suggest that the drug's

55 e PDB2PQR web server addresses this need for electrostatic field calculations.

56 arison to structural models, that changes in electrostatic field can be measured within the complex p

57 Oriented electrostatic fields can exert catalytic effects upon bo

58 k provides direct experimental evidence that electrostatic fields can tune the redox potentials of ch

59 Electrostatic field changes as large as -10 MV/cm were o

60 tional Stark spectroscopy, we quantified the electrostatic field changes within the surrounding activ

61 d for each fragment, and a set of steric and electrostatic fields ("CoMFA column") is generated for e

62 eloped which uses electrodynamic rather than electrostatic fields commonly used in drift cell IM-MS i

63 eaction field approach, we have computed the electrostatic field contributions to the fluorine shield

64 Although the relative steric and electrostatic field contributions were similar to those

65 Tyr 149 is attributed mainly to the positive electrostatic field created by NAD+ and Lys 153 (4.5 kca

66 binding sites and appears to be bound by the electrostatic field created by the cationic residues, wi

67 tions report differences in the intraprotein electrostatic field, demonstrating that the dipole or ch

68 The alignment of a dipole with the local electrostatic field depends on both the topology of the

69 The electrostatic field distribution about RbfADelta25 is bi

70 the KH domain of the E.coli Era GTPase, its electrostatic field distribution is most similar to the

71 e observed shift in nuC=O, originates in the electrostatic field due to the alpha-helix dipole from r

72 nescent circular polarization by applying an electrostatic field due to the electrical tunability of

73 quantitative and directional probes of local electrostatic fields, due to the vibrational Stark effec

74 p between 250 km and 768 km from a planetary electrostatic field (E( )(+) = 1.09 +/- 0.17 muV m(-1))

75 used in semiconductor-based devices via the electrostatic field effect, would be far more versatile

76 by the complex, implicating a through-space electrostatic field effect.

77 output characteristics, which also points to electrostatic (field-effect) charging.

78 est since they demonstrate the importance of electrostatic field effects on Phe and Tyr C gamma chemi

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

80 shown to require a good description of local electrostatic field effects, and we find the best result

81 and under submerged conditions in different electrostatic fields (EFs) and were assessed for cell vi

82 A positive electrostatic field emanating from the center of the aqu

83 We demonstrate that long-range electrostatic fields emanating from the oxide lead to st

84 The enhanced electrostatic field enables a 64-fold increase in dipole

85 microelectromechanical devices with dynamic electrostatic fields enabling strong coupling between ot

86 Ala "NPA" motifs), together with the protein electrostatic fields enforce a bipolar water configurati

87 h atomic precision, thereby tuning the local electrostatic field experienced by single manganese (Mn)

88 Water-dominated electrostatic field fluctuations bring *Re and CS1 state

89 nformations show the best alignment with the electrostatic field, followed by residues in beta-strand

90 frequency correlates linearly with the local electrostatic field for both hydrogen-bonding and non-hy

91 The contributions from steric and electrostatic fields for model 1 were 0.621 and 0.379, r

92 The contributions from steric and electrostatic fields for model 2 were 0.493 and 0.507, r

93 tion band potential difference and the inner electrostatic field formed in the p-n heterojunction pro

94 These results suggest that the negative electrostatic field from the two opposing Asp carboxylat

95 It is the SHG sensitivity to the electrostatic field generated by a charged interface tha

96 An effective way to characterize the electrostatic field generated by nucleic acids is to qua

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

98 tely attenuates the DNA charge and hence the electrostatic field generated by the molecule.

99 f peptide bond dipole moments with the local electrostatic field generated by the rest of the molecul

100 ctivity), indicating a role for the positive electrostatic fields generated by both ABEs in enhancing

101 omplex formation with complementary negative electrostatic fields generated by FV.

102 Stark spectroscopy, and NMR studies revealed electrostatic field heterogeneity of 8 MV/cm between act

103 t are extremely confined and controllable by electrostatic fields; however, electrical detection of p

104 s simulations in the presence of a transpore electrostatic field (i.e., a voltage drop along the pore

105 (2).(-), HO., etc.) and a strong interfacial electrostatic field (IEF of 10(9)~10(10) V/m).

106 n equation, quantitative computations of the electrostatic field in a sodium channel structural model

107 Using an electrostatic field in a split-gate geometry to independ

108 es can provide a direct readout of the local electrostatic field in complex molecular environments, s

109 d mixed states, have been revealed within an electrostatic field in range of -2 V to + 2 V, as well a

110 In this mechanism, the electrostatic field in the catalytic site turns the elec

111 k is largely governed by the presence of the electrostatic field in the cavity, which is reflected by

112 ectivity due to steric and/or an anisotropic electrostatic field in the distal heme pocket being resp

113 stead, it was indicative of an alteration of electrostatic field in the permeation pathway.

114 The role of the RNA electrostatic field in this interaction was explored usi

115 tark effect spectroscopy was used to measure electrostatic fields in the hydrophobic region of the ac

116 Calculation of difference electrostatic fields in the pore model predicted that li

117 ompensation of reduced fluctuations of local electrostatic fields in the presence of an apolar solute

118 d the sensitivity of carbonyl frequencies to electrostatic fields, including those due to hydrogen bo

119 t of the red-shift in the LSP energy and the electrostatic field induced blue shift in the PL energy

120 tion through pores formed via an ion-induced electrostatic field is a viable mechanism for unassisted

121 associated electrostatic fields, whereas the electrostatic field is less sensitive to the particular

122 Electrostatic field lines reveal attraction across the c

123 ized structures with significantly different electrostatic field magnitudes at the CO ligand site ind

124 The electrostatic field of Earth is strong enough by itself

125 ccelerating effect of the negatively charged electrostatic field of FS on the diffusion of metal ions

126 The electrostatic field of the crystal is used to generate a

127 erations in this asymmetric yet strong local electrostatic field of the EEDD ring significantly alter

128 enhanced by favorable interactions with the electrostatic field of the enzymes.

129 Increasing the positive electrostatic field on PC by the addition of a Zn(2+) io

130 use protein architecture to impose specific electrostatic fields onto their bound substrates, but th

131 These results suggest the dominance of an electrostatic field polarization model in which increasi

132 ion of monomers and clusters in their mutual electrostatic field proceeds in a fractal manner.

133 Applying external electrostatic fields produced a transmembrane ionic curr

134 This position may serve to enhance the electrostatic fields produced by this basic domain at th

135 to charge difference may be mediated by the electrostatic field provided by anionic phospholipids.

136 We concluded that the large local negative electrostatic field shifted the outer vestibule carboxyl

137 ctrostatic polarization" mechanism, in which electrostatic fields significantly polarize charge distr

138 formation on the time-dependent variation in electrostatic field strength on the Bchl and Bph cofacto

139 est that the RNA duplex generates a stronger electrostatic field than DNA, as is predicted based on t

140 er - electrons and nuclei - results in local electrostatic fields that are ubiquitous in nanoscale st

141 ts in materials give rise to fluctuations in electrostatic fields that reflect the local charge densi

142 tatic steering of ligands with complementary electrostatic fields, the second (specific) involves a c

143 We find that variations of the protein electrostatic field through the channel, owing to preser

144 led by reprotonated His-322 and drift in the electrostatic field toward the cytosol.

145 Electrostatic fields tune the ground state of interfaces

146 Steric and electrostatic fields were calculated for a training set

147 Measured electrostatic fields were compared to predictions based

148 significant differences among the associated electrostatic fields, whereas the electrostatic field is

149 phobic cores of these peptides support local electrostatic fields which result in nativelike heme chr

150 e relying on an inherent transverse focusing electrostatic field, which induces transverse oscillatio

151 Few specificity annotation methods consider electrostatic fields, which play a critical role in mole

152 ph) cofactors that provide natural probes of electrostatic fields within this protein.