ライフサイエンスコーパス: electrostatic field

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

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

3 e energetic consequences of the nucleic acid electrostatic field.

4 calibrates their vibrational frequencies to electrostatic field.

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

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

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

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

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

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

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

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

13 from artificially created electromagnetic or electrostatic fields.

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

15 vity with observed differences in steric and electrostatic fields.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

32 Electrostatic field assistance is applied to improve NP

33 This electrostatic field-assisted carrier separation and perc

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

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

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

37 Electrostatic field calculations suggest that the drug's

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

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

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

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

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

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

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

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

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

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

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

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

50 The electrostatic field distribution about RbfADelta25 is bi

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

88 Electrostatic field lines reveal attraction across the c

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

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

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

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

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

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

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

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

97 Applying external electrostatic fields produced a transmembrane ionic curr

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

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

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

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

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

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

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

105 Electrostatic fields tune the ground state of interfaces

106 Steric and electrostatic fields were calculated for a training set

107 Measured electrostatic fields were compared to predictions based

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

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

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

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

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