ライフサイエンスコーパス: orientational

1 cells where interfacial interactions pattern orientational alignment in the matrix phase, which proba

2 tween two intense THz pulses, we control the orientational alignment of molecules in a liquid, and no

3 the deposition of highly crystalline films, orientational alignment of polymer chains, albeit common

4 ed phase to a nematic phase characterized by orientational alignment of rod-like cells.

5 R-based method of infrared transition moment orientational analysis (IR-TMOA) is employed to unravel

6 eaks and provides the possibility to perform orientational analysis.

7 nsemble dynamics provides a means to extract orientational and dynamic information of TM helices from

8 control over the assembly, in particular the orientational and electronic structure, providing a flex

9 Moreover, orientational and positional analyses show that TAM exhi

10 Taking into account both orientational and positional constraints, we investigate

11 otropic fluids that possess only short-range orientational and positional order, in which the only ma

12 ing the four peripheral domains and imposing orientational and positional restraints on the other dom

13 residual dipolar couplings (which yield both orientational and shape information) and solution X-ray

14 rs that contribute to indole's and benzene's orientational and spatial distribution.

15 ned electrostatic interactions to guide both orientational and triclinic positional self-ordering of

16 ete systematic search of the conformational, orientational, and positional space of the docked ligand

17 ices of tract volume and hindrance-modulated orientational anisotropy (HMOA).

18 rsal cingulum volume and hindrance-modulated orientational anisotropy was significantly reduced in th

19 ipid acyl tails, and changes the spatial and orientational arrangement of lipid headgroup atoms.

20 ounter states and identified the spatial and orientational aspects.

21 igner glass) and a second one, stabilized by orientational attractions (Disconnected House of Cards g

22 e contributions to the former are incomplete orientational averaging during the donor lifetime and, b

23 eation, support an electrostatic rather than orientational basis for proton exclusion.

24 Two types of orientational behavior emerged.

25 characterized by using ellipsometry and the orientational behavior of liquid crystals.

26 ly oriented RNase A was also apparent in the orientational behavior of nematic liquid crystals of 4-c

27 pport for our dynamic model of a significant orientational bias of Ub toward a more closed conformati

28 tronic structures of BN acene compounds: (1) Orientational BN isomers have similar HOMO-LUMO gaps.

29 (2) For each pair of orientational BN isomers, the more thermodynamically sta

30 nal symmetry), and quasi-crystalline (having orientational but not periodic translation symmetry) pha

31 t cycle and the sugar is found to undergo an orientational change in order to escape the protein lume

32 Ring D orientational change in the electronic excited state to

33 related with the ordering of 1-hexanol is an orientational change of the cyclohexane solvent from fla

34 ne, however, do not describe the majority of orientational changes in the water molecules in the firs

35 omputational model to understand and predict orientational changes of surface-anchored nematic liquid

36 Detailed translational and orientational characteristics of these superstructures w

37 e is spatially disordered, yet has molecular orientational characteristics that distinguish it from a

38 fractional anisotropy (FA), a measure of the orientational coherence of water self-diffusion, is regi

39 TectoRNAs programmed to assemble with orientational compensation produce micrometer-scale RNA

40 rfaces of the molecules have attained a high orientational complementarity by the time the TS is reac

41 used a novel diffusion MRI method, diffusion orientational complexity (DOC), as an index of grey matt

42 ion of these restrained local minima for the orientational configuration in which they were most pron

43 complement to NOE data in that they provide orientational constraints as opposed to distance constra

44 labeled acetyl groups and the extraction of orientational constraints from residual dipolar coupling

45 Altogether using orientational constraints from SSID and experimental alp

46 domain blocked with amantadine, built using orientational constraints obtained from solid-state NMR

47 We find that the main benefits of orientational control are that (i) it allows rapid adjus

48 The magnetic orientational control enables instant and selective exci

49 The main reason for the efficiency of orientational control in regulation of fimbriation level

50 faces enable conformational, topological and orientational control of tectoRNA self-assembly.

51 This method exploits the high spatial and orientational control of the protein monolayer assembly

52 Orientational control of the scaffold protein STM, a tri

53 trol." We present two families of models for orientational control to understand the details of how i

54 riation is controlled by a mechanism called "orientational control." We present two families of model

55 The orientational correlation function obtained from PSPP ex

56 on function, two-point probability function, orientational correlation function, specific surface, an

57 both the out-of-plane and "mainly"-in-plane orientational correlation functions in a model-independe

58 Analysis to the level of the orientational correlation functions shows that the liqui

59 hanced for elongated active particles due to orientational correlations in their direction of propuls

60 erature dependence of the relaxation time of orientational correlations is decoupled from that of the

61 simulations quantitatively characterized the orientational correlations of DNA in DNA arrays as well

62 Orientational correlations up to nearest neighbor molecu

63 Orientational data allow excluding a ZZZasa geometry and

64 The derived orientational data indicate a local helix tilt ranging f

65 In contrast, orientational data on ring A show no rotation of ring A

66 dx-CYP101 complex, a combined approach using orientational data on the two proteins derived from resi

67 el derived from previous solid-state NMR 15N orientational data.

68 Here, we apply the DF theory to systems with orientational degrees of freedom as well as anisotropic

69 Furthermore, the role played by optical orientational degrees of freedom is established.

70 nt confusion in the literature regarding the orientational dependence of linear dichroism.

71 ng the hyperfine splittings gleaned from the orientational dependent EPR spectra.

72 cal tilt can be directly calculated from the orientational-dependent hyperfine splitting in the EPR s

73 However, subtle orientational differences cause strong distinctions in s

74 Additional orientational differences of subdomains within the lobes

75 bbling-in-a-cone model describing restricted orientational diffusion that is followed by complete ori

76 recognition, discrete aggregation number and orientational discrimination of coiled-coil protein doma

77 lipids surrounding the beta-barrel have high orientational disorder and chain upturns, thus they may

78 choline (PC) bilayers, RTD-1 causes moderate orientational disorder independent of the bilayer thickn

79 The ultrafast orientational disorder of molecular dipoles, activated a

80 Orientational disorder of the distal nitrosyl (NO) ligan

81 rmore, all defect types feature a pronounced orientational disorder of the OH groups, which results i

82 ransition and the accompanied freezing-in of orientational disorder of the stilbene molecule.

83 phatidylglycerol lipids induces much greater orientational disorder without affecting the dynamic dis

84 bsence of ATP, BSL-S1 showed almost complete orientational disorder, as reported previously for the w

85 n the presence of PG-1 but shows significant orientational disorder.

86 to the PC bilayer significantly reduces this orientational disorder.

87 rol to the POPC membrane does not affect the orientational disorder.

88 irected along the modified strand, there are orientational distinctions that are sequence dependent a

89 describe the relationship between the chain orientational distribution and WAXS data was used to obt

90 The obtained orientational distribution functions of carotenoids and

91 The theory of orientational distribution functions was adapted to live

92 d that the LCD of cross-linked fibers has an orientational distribution intermediate between relaxati

93 The orientational distribution of fluorophores is an importa

94 concentrations investigated, with an oblate orientational distribution of the phospholipids at a pep

95 limit oscillation (spectrum-dependent on the orientational distribution only) and slow restricted mot

96 thod is that no specific model for a complex orientational distribution was presumed.

97 t on the rotational correlation time and the orientational distribution).

98 d in the accompanying work, we find that two orientational distributions are necessary to fit the WAX

99 ve been widely used for imaging biomolecular orientational distributions in protein aggregates, fibri

100 Orientational distributions of these actions suggest tha

101 Notably, a strong effect of the orientational doping on the fluorescence quantum yield w

102 The orientational dynamics (time-dependent anisotropy), whic

103 troscopy was developed and used to study the orientational dynamics of a planar alkylsiloxane monolay

104 It is shown that the orientational dynamics of a single transition can be tra

105 Here we report distinct orientational dynamics of reverse transcriptase observed

106 The orientational dynamics of water at a neutral surfactant

107 We report on the orientational dynamics of water at an extended hydrophob

108 Examination of the orientational dynamics points to a faster relaxation in

109 ave attributed this dependence to the cell's orientational dynamics within the trap.

110 escence by DNA, makes it a good probe of DNA orientational dynamics.

111 Orientational effects are apparent at the surface; e.g.,

112 conformations on entropic grounds, although orientational effects may play an additional role.

113 BD simulations reveal both translational and orientational electrostatic steering of the PH domain to

114 Translational and orientational excluded-volume fields encoded in particle

115 We also find that the critical FRET orientational factor kappa(2), has an average value and

116 ed by X-ray diffraction analyses as a unique orientational feature of the nickel-dithiolate ligands i

117 act with emergent topological defects in the orientational field of the nematic director.

118 fields-the velocity field and the molecular orientational field.

119 n a well-defined interface, enabling desired orientational flexibility and enhanced access of binding

120 Histograms of orientational fluctuations from fluorescent molecules in

121 We examined the orientational fluctuations of a small number of myosin m

122 ndependent of x, and is interpreted as small orientational fluctuations that occur without hydrogen-b

123 tructure ensemble shows significantly larger orientational fluctuations while the ensemble-averaged o

124 le phase separation initiated by density and orientational fluctuations.

125 ropic force originates from reduction of the orientational freedom of anisotropic analytes in small p

126 ows the power of this approach for measuring orientational information in biologically important RNA

127 ults in single-line spectra that contain the orientational information necessary for protein structur

128 Neither orientational information nor the resulting genomic rear

129 mics (MD) simulations provide structural and orientational information of high precision and accuracy

130 lk proteins, determination of structural and orientational information of interfacial proteins, e.g.,

131 s of such profiles provides a rich source of orientational information.

132 ention that FRET data can be used to provide orientational information.

133 me isomers: a major (M) and a minor (m) heme orientational isomer related by a 180 degrees rotation a

134 The thermodynamics of substrate orientational isomerism are mapped for substrates with i

135 so resulted in a change in the ratio of heme orientational isomers, in a likely manifestation of heme

136 s indicate the existence of both spatial and orientational long-range order in the packing, which is

137 namic optical tuning can be achieved through orientational manipulation of free-standing super-parama

138 Upon deviatoric stress-driven orientational migration, the intraparticle coalescence o

139 -CaM complexes characterized by high and low orientational mobilities, with the low-mobility populati

140 In the absence of ATP, the orientational mobility distributions are similar for CaM

141 opulation of PMCAox-CaM complexes with a low orientational mobility in the presence of ATP, whereas n

142 modulation spectroscopy, which measured the orientational mobility of fluorescently labeled CaM boun

143 olarization methods were used to measure the orientational mobility of fluorescently labeled oxidized

144 The orientational mobility of PMCA-CaM complexes was determi

145 unable to discriminate between the intrinsic orientational mobility of the fluorophore labels and the

146 complexes appears with significantly reduced orientational mobility.

147 spinning NMR and uniformly aligned samples (orientational mosaicity of <1 degrees ) for oriented-sam

148 the decay of vibrational correlations and re-orientational motion that is in better agreement with ex

149 drop at very short times caused by inertial orientational motion, followed by a much slower decay th

150 The tQD provides an orientational optimization of the interfacial and filler

151 exhibit colloidal anisotropy with very high orientational order and are characterized by SAXS as sho

152 ular chirality, as the only requirements are orientational order and curved shape of confinement.

153 ystalline block copolymers exhibit excellent orientational order and lateral order.

154 lient feature is strong coupling between the orientational order and mechanical strain.

155 matter in which molecules show a long-range orientational order and no positional order is called a

156 tive analytical connection between the local orientational order and the elasticity in model amorphou

157 self-assembly, but their effects on emergent orientational order are not well understood when anisotr

158 rotron small-angle X-ray scattering to probe orientational order as a function of water content and o

159 hese spheroid-like particles showed a unique orientational order associated with the alignment of the

160 Molecules exhibit orientational order at nanometer length scales, while ch

161 with aligned flows and textures that feature orientational order at the millimeter scale.

162 Orientational order can be affected by changes in extern

163 have been conducted to study to what degree orientational order can be further improved by combining

164 (LCLCs) as these materials show spontaneous orientational order caused by unidirectional stacking of

165 orm four well-controlled bend distortions as orientational order changes.

166 At the core of these defects, the orientational order drops sharply.

167 theory predicts that, in packings, the local orientational order due to excluded-volume causes less n

168 The structural control of orientational order enabled by the atomic precision of S

169 ication of the composition and the degree of orientational order in the domains.

170 se techniques do not give access to complete orientational order information in a whole image, becaus

171 Molecular orientational order is also seen to be affected by chole

172 lf-assembly for anisotropic systems in which orientational order is desired, such as when tailored me

173 structures with long-range translational and orientational order is sensitive to the molecular intera

174 oncomitantly with a transition in the bundle orientational order near the surface and is controlled b

175 c non-Newtonian fluids, characterized by the orientational order of a director field SE pointing arro

176 that retrocyclin-2 selectively disrupts the orientational order of anionic membranes while leaving z

177 ium phase characterized by a system-spanning orientational order of defects.

178 l flexibility of the label but also to image orientational order of filaments at the nanoscale using

179 ticles, such as trefoil knots, with 'frozen' orientational order of flakes.

180 l to the flat surfaces of the particles, the orientational order of lipid acyl chains is low and inco

181 unique feature of nematic liquid crystals is orientational order of molecules that can be controlled

182 a method to quantify proportions of the bond-orientational order of nearest neighbor clusters in coll

183 es within 2 min of deposition, increased the orientational order of specific polymorphs, and promoted

184 n the activity-triggered flow and long-range orientational order of the medium.

185 nanoporous channels control the diameter and orientational order of the silver nanoparticles.

186 anipulation of the vibrational landscape and orientational order of the superatoms.

187 The co-orientational order parameter (COOP) was based on the ma

188 ical framework of a classical parameter, the orientational order parameter (OOP).

189 and WAXS data was used to obtain an average orientational order parameter, S(x-ray).

190 e-angle x-ray scattering yielded the S(xray) orientational order parameter.

191 of oriented lipid bilayers to measure chain orientational order parameters and lipid areas in model

192 olipids, C20BAS-PC exhibits a high degree of orientational order throughout the membrane and the sn-1

193 led lipid and polarized light imaging of the orientational order within the thin film of nematic 5CB.

194 nsition is accompanied by the change of bond-orientational order without noticeable change in density

195 ransition is much lower for liquid crystals (orientational order) than for plastic solids (translatio

196 sfer must be faster the stronger the group's orientational order, a prediction accurately verified by

197 lic glass has no long-range translational or orientational order, although some degrees of short- and

198 changes in structure and bonding, molecular orientational order, and electronic structure of dense h

199 ar vesicles does not yield information about orientational order, and the scattering from the Lo and

200 terials or micromaterials displaying precise orientational order, realization of dry superlattices as

201 To quantify orientational order, we used a novel algorithm to charac

202 AXS pattern due to an increase in acyl chain orientational order, which is one of the main properties

203 assemble into short, metastable strands with orientational order-regardless of the final structure.

204 nsionality according to their micromolecular orientational order.

205 ticles immersed in liquid crystals frustrate orientational order.

206 tion of superlattices with translational and orientational order.

207 with predictions for systems exhibiting weak orientational order.

208 rocessing of BCP films to achieve long-range orientational order.

209 ilding blocks exhibiting the lowest symmetry orientational order.

210 rearrange in regions of low density and bond orientational order.

211 e phases with both long-range positional and orientational order.

212 ing characterization of changes in molecular orientational ordering associated with solid-state phase

213 ize, and tablet stacking direction show that orientational ordering occurs not abruptly but gradually

214 h we disperse in nematic fluids that possess orientational ordering of anisotropic rod-like molecules

215 Orientational ordering of graphene oxide flakes in self-

216 lity, and phosphorylation on the macroscopic orientational ordering of LCs supported on these surface

217 We study orientational ordering of membrane compounds in the myel

218 The behaviour is modelled as a function of orientational ordering of nanotubes induced by the uniax

219 cubic (bcc) superlattices which also exhibit orientational ordering of NCs in their lattice sites.

220 We have examined the orientational ordering of nematic liquid crystals (LCs)

221 ield of the excitation transfer process, the orientational ordering of peripheral chlorophylls does n

222 a(+)) and soft (Ag(+)) cations to direct the orientational ordering of polar oxyfluoride building uni

223 e, but the combination of Na/Ag ordering and orientational ordering of the [MO(3)F(3)](3-) anions pro

224 This orientational ordering of the FG domains depends on thei

225 of dipeptides are transduced via macroscopic orientational ordering of the LCs.

226 actions and show how triclinic crystals with orientational ordering of the semiconductor nanorods eme

227 ce of water layers adjacent to the solid and orientational ordering therein.

228 erating spheroid-like particles and also the orientational orders observed in the self-assembly of th

229 model whereby local geometry constrains the orientational organization of the FG nups.

230 proteins are ordered, indicating an overall orientational organization within the NPC.

231 parameters in the sample such as lipid type, orientational organization, and composition.

232 We find that the orientational pattern of the filaments is in accord with

233 Sensitivity of bacteria to preimposed orientational patterns represents a previously unknown f

234 Exploration of the orientational phase-space revealed that the placement of

235 tism in bulk compounds, novel electronic and orientational phases in thin films and quantum transport

236 the confining walls, the competition between orientational polarization and angle preferences of inte

237 ed to evaluate the contribution of a solvent orientational polarization, correlated by the network of

238 st and the developmental requirements of the orientational preference map.

239 Our 3D atomic models reveal that such orientational preference results from asymmetric binding

240 eas in the D219/E220 deletion mutant, little orientational preference was observed.

241 NmHO exhibits significantly stronger orientational preference, reflecting much stronger and s

242 Orientational preferences between interacting helices wi

243 interactions contribute to the stability and orientational preferences of the dimers.

244 e the design of macromolecules with specific orientational preferences, as well as nanometer-scale me

245 a sensitive technique for imaging the local orientational properties of anisotropic materials, inclu

246 as been shown to be a sensitive probe of the orientational properties of individual molecules and/or

247 lying X-ray dichroism to determine molecular orientational properties of other materials, especially

248 itative analysis of the X-ray dichroism, the orientational properties of the C-I bonds within this ma

249 ed techniques do not provide insights on the orientational properties of the guest molecules.

250 onal clusters with regular translational and orientational protein arrangements, which may allow cell

251 ys and eventually give rise to two different orientational pseudorotaxane isomers.

252 s designed to validate the exchange-mediated orientational randomization (EMOR) model used to interpr

253 ional diffusion that is followed by complete orientational randomization described as jump reorientat

254 he relatively large pore sizes, the complete orientational randomization of CO2 and structural fluctu

255 on (wobbling-in-a-cone) followed by complete orientational randomization on a time scale of 900 +/- 2

256 The complete orientational randomization, slows from 136 ps in the bu

257 mponent is a measure of the rate of complete orientational randomization, which requires H-bond rearr

258 nt lattice to a 'twin' lattice, producing an orientational relationship akin to that of the conventio

259 nvestigated by observing spectral diffusion, orientational relaxation and population relaxation using

260 Proton-transfer kinetics and orientational relaxation are measured by time-dependent

261 n, the excited-state proton transfer and the orientational relaxation are similar to those observed f

262 nt anisotropy measurements yield the rate of orientational relaxation as a function of x.

263 The comparison of water orientational relaxation at neutral and ionic interfaces

264 mode to determine vibrational relaxation and orientational relaxation dynamics.

265 The water orientational relaxation has a fast component of a few p

266 nite exhibit temperature-dependent diffusive orientational relaxation in a restricted cone of angles.

267 The slowest component of the orientational relaxation increases from 2.6 ps (pure wat

268 Orientational relaxation is analyzed with a wobbling-in-

269 hroism measurement, characterized picosecond orientational relaxation of the headgroup occurring at t

270 xyl stretch, and the results are compared to orientational relaxation of water interacting with an io

271 The short-time orientational relaxation of water is studied by ultrafas

272 Pump-probe measurements of the orientational relaxation rates and vibrational lifetimes

273 The results demonstrate that the orientational relaxation times for interfacial water mol

274 s a pivotal role in translational as well as orientational relaxation.

275 e corresponding proton-transfer kinetics and orientational relaxation.

276 PSPP measurements observed only inertial orientational relaxation.

277 pled with conformational, translational, and orientational restraining potentials can be computationa

278 coming some of these challenges by utilizing orientational restraints from residual dipolar couplings

279 ing paramagnetic distance restraints and NMR orientational restraints in the form of backbone (15)N r

280 ar couplings were used to provide long range orientational restraints, and long range (|i - j| > or =

281 Oriented-sample data yielded orientational restraints, whereas magic-angle spinning d

282 packing of nanoparticles into crystals with orientational, rotational, and translational orders.

283 tions of the T4 lysozyme are associated with orientational rotations.

284 en state, likely due to a conformational and orientational selection of permeating molecules.

285 Orientational selectivity is not observed.

286 The high resolution and orientational selectivity of HF electron-nuclear double

287 The high resolution and orientational selectivity of HF ENDOR allows us to direc

288 Nematic-like and helicoidally orientational self-assemblies of gold nanorods co-disper

289 unique growth mechanism based on long-range orientational self-assembly.

290 t selective activation by PI(4,5)P2 involves orientational specificity and that other PIPs inhibit th

291 ed in this article also demonstrate that the orientational states of proteins immobilized at surfaces

292 he bilayer is nearly optimal to both enhance orientational steering and to localise GRP1-PH proximal

293 such droplets condensate or melt and how the orientational symmetry is broken remains however unclear

294 lation symmetry), amorphous (no periodic and orientational symmetry), and quasi-crystalline (having o

295 imposed by the boundaries and the intrinsic orientational symmetry-breaking of these materials gives

296 Such an orientational tuning expands the possibilities for elect

297 Orientational uncertainty may be the major contributor t

298 data can be simulated from the model only if orientational variability is introduced for the P5 and,

299 embles of more than two replicas show larger orientational variations similar to those observed in th

300 h interplay between topology, chirality, and orientational viscoelasticity.A skyrmion is a topologica