ライフサイエンスコーパス: small angle

1 bination of synchrotron X-ray diffraction at small angles and in situ rheology (rheo-SAXS) experiment

2 We use small-angle and total X-ray scattering, dynamic light sc

3 We used time-resolved small-angle and wide-angle x-ray scattering simultaneous

4 iques such as X-ray and neutron diffraction, small-angle and wide-angle X-ray scattering, free-electr

5 t required endocyclic transition states with small angles between the bond being formed to the nucleo

6 Remarkably, we found that the small-angle data primarily detect modulations of the sol

7 ombined small angle X-ray scattering (SAXS), small angle neutron scattering (SANS) and low-pressure N

8 monstrate the coupling of microfluidics with small angle neutron scattering (SANS).

9 Small angle neutron scattering and circular dichroism sp

10 f lipid bilayer's response to Abeta binding, Small Angle Neutron Scattering and Neutron Membrane Diff

11 scattering, small angle X-ray scattering and small angle neutron scattering data of the colloidal dis

12 ing atomic force microscopy and supported by small angle neutron scattering solution data.

13 Another rHDL model based on small angle neutron scattering supported a double superh

14 ipsometry and ion beam analysis, while using small angle neutron scattering to characterise the morph

15 ted with charged lipid bilayers, we employed Small Angle Neutron Scattering to probe lipid distributi

16 c force microscopy, static light scattering, small angle neutron scattering, and UV-vis spectroscopy.

17 canning transmission electron microscopy and small angle neutron scattering.

18 of-the-art atom-probe tomography and in situ small angle neutron scattering.

19 rdered phycobilisome structure, evident from small-angle neutron and X-ray scattering and cryo-transm

20 at the same pressures on the General-Purpose Small-Angle Neutron Scattering (GP-SANS) instrument at O

21 lid-state magic-angle spinning (MAS) NMR and small-angle neutron scattering (SANS) were consistent wi

22 An integration of small-angle neutron scattering (SANS), low-pressure N2 p

23 employing an integrative approach combining small-angle neutron scattering (SANS), low-resolution el

24 eric AtCESA1CatD proteins were studied using small-angle neutron scattering and small-angle x-ray sca

25 pported by structural characterization using small-angle neutron scattering and X-ray diffraction.

26 It is shown that the acquisition of small-angle neutron scattering data at two different sol

27 ta-D-Maltoside and from previously published small-angle neutron scattering experimental data of the

28 Consistent with this observation, small-angle neutron scattering indicates that the dimens

29 In the present study neutron diffraction and small-angle neutron scattering measurements of adsorbed

30 Small-angle neutron scattering reveals vastly different

31 However, small-angle neutron scattering, electron-microscopy imag

32 Using a combination of solution-state NMR, small-angle neutron scattering, small-angle X-ray scatte

33 um sulfosuccinate) in n-octane liquids using small-angle neutron scattering, thermal conductivity mea

34 formational equilibrium of this enzyme using small-angle neutron scattering, under conditions where w

35 anoparticle tracking analysis, and light and small-angle neutron scattering.

36 nuclear magnetic resonance spectroscopy and small-angle neutron scattering.

37 revious modeling of its trimeric nature from small angle scattering (SAXS) data.

38 es were determined by numerical inversion of small angle scattering and isothermal magnetisation data

39 ains-determined by X-ray crystallography and small angle scattering-as well as kinetics experiments d

40 d transmission electron microscopy and X-ray small angle scattering.

41 flectivity (XRR) and grazing incidence X-ray small-angle scattering (GISAXS) reveal that unfunctional

42 Small-angle scattering (SAS) has a proven ability to det

43 The model incorporates the improved small-angle scattering approximation (SAA) to radiative

44 Despite the ever-increasing usage of small-angle scattering as a valuable complementary metho

45 estoration of soluble protein structure from small-angle scattering data, we construct a general mult

46 We compute small-angle scattering intensities, pore size distributi

47 Small-angle scattering of x-rays (SAXS) and neutrons (SA

48 atial beam modulation, allows for mapping of small-angle scattering signals and hence addressing micr

49 idopsis thaliana; AtCESA1CatD) determined by small-angle scattering techniques and provides the first

50 Small-angle scattering tensor tomography is applicable t

51 Combined small-angle scattering with X-rays and neutrons coupled

52 termine how interstitials are annihilated at small-angle tilt GBs (STGBs) in SiC.

53 Here, we report on the observation of small angle twist sub-grain boundaries in a typical MAX

54 Therefore, small angle x-ray experiments have been performed to inv

55 nced sensitivity to trypsin digestion and by small angle x-ray scattering (SAXS) analysis.

56 Here, small angle X-ray scattering (SAXS) and mutational analy

57 f symmetry Fd3m (Q227) which was verified by Small angle X-ray scattering (SAXS) and Transmission ele

58 Small angle X-ray scattering (SAXS) confirms the disrupt

59 crystal structures of MotB fragments to the small angle X-ray scattering (SAXS) data revealed that t

60 Small Angle X-ray Scattering (SAXS) is an increasingly c

61 Small angle X-ray scattering (SAXS) is used to confirm s

62 Small angle x-ray scattering (SAXS) measurements and che

63 A small angle X-ray scattering (SAXS) pattern shows the pe

64 The low-resolution small angle X-ray scattering (SAXS) results show that th

65 Small angle X-ray scattering (SAXS) revealed no fixed or

66 Small angle X-ray scattering (SAXS) reveals a flexible m

67 multi-domain constructs in combination with small angle X-ray scattering (SAXS) to determine the str

68 We have combined x-ray crystallography with small angle x-ray scattering (SAXS) to elucidate the str

69 We combine small angle X-ray scattering (SAXS) with ensemble-optimi

70 Using turbidity assays, time-resolved small angle X-ray scattering (SAXS), and time-resolved n

71 Small angle X-ray scattering (SAXS), electrospray ioniza

72 of the pore structure using a combination of small angle X-ray scattering (SAXS), low-pressure N2 and

73 o estimate fractal dimensions using combined small angle X-ray scattering (SAXS), small angle neutron

74 Using NMR, isothermal calorimetry (ITC), and small angle x-ray scattering (SAXS), we dissect binding

75 combined x-ray crystallography of Pcore with small angle x-ray scattering (SAXS)-based ensemble model

76 were recombinantly expressed and studied by small angle x-ray scattering (SAXS).

77 rcine bile, were identified by (13)C NMR and small angle X-ray scattering (SAXS).

78 emonstrate self-sorting by NMR, rheology and small angle X-ray scattering (SAXS).

79 s indicated by behavioral, birefringence and small angle X-ray scattering analyses.

80 Small angle X-ray scattering analysis (SAXS) supports th

81 Small angle x-ray scattering analysis shows that RIFMO d

82 s well as the unbound zymogen C2 obtained by small angle x-ray scattering analysis.

83 Supported by solution small angle x-ray scattering and a combination of site-d

84 onomeric or dimeric, providing the basis for small angle x-ray scattering and chemical cross-linking

85 Small angle X-ray scattering and ensemble modeling yield

86 entire ESCRT binding region of HD-PTP using small angle X-ray scattering and hydrodynamic analyses.

87 rmined the MBD1-3 conformational space using small angle X-ray scattering and identified changes in M

88 isting under solution conditions, we applied small angle x-ray scattering and isotope-assisted chemic

89 f a full-length structural model produced by small angle x-ray scattering and its implications for th

90 Biophysical analysis, using small angle X-ray scattering and multi-angle light scatt

91 ourier transform of static light scattering, small angle X-ray scattering and small angle neutron sca

92 We have used small angle x-ray scattering at a high intensity synchro

93 sm, a molecular envelope was calculated from small angle X-ray scattering data for the Bacillus subti

94 n with prephenate bound and the accompanying small angle x-ray scattering data reveal the molecular m

95 esolution structural information obtained by small angle X-ray scattering data suggests that RecQ4 in

96 data, both size exclusion chromatography and small angle x-ray scattering data support a tetrameric a

97 Finally, small angle x-ray scattering demonstrates that the AmpR.

98 eport on a method to obtain angular-resolved small angle x-ray scattering distributions with edge-ill

99 ttering, analytical ultracentrifugation, and small angle X-ray scattering each provide evidence that

100 Moreover, with the aid of small angle X-ray scattering experiments, we also determ

101 ttering, analytical ultracentrifugation, and small angle x-ray scattering experiments.

102 Small angle X-ray scattering indicates that FP E244K is

103 Small angle x-ray scattering indicates that sCT monomers

104 analysis of the F1L N-terminal regions using small angle x-ray scattering indicates that the region o

105 Small angle x-ray scattering measurements of prothrombin

106 When compared to the small angle x-ray scattering measurements, the model fit

107 A small angle x-ray scattering model of SmTK-TSA in soluti

108 Small angle x-ray scattering showed that the linking reg

109 Here, we determined a conjoined NMR-small angle x-ray scattering structure of the EV71 SLII

110 These small angle X-ray scattering studies indicated that GstD

111 nges while size-exclusion chromatography and small angle X-ray scattering studies indicated that hepa

112 The atomic structure and Small Angle X-ray Scattering studies of a 97 kDa fragmen

113 Small angle X-ray scattering studies show that the 'Open

114 In addition, small angle X-ray scattering studies together with accom

115 Using small angle X-ray scattering studies, models of predomin

116 Using a combination of x-ray and small angle x-ray scattering studies, we reveal unique f

117 lysis by optical microscopy, calorimetry and small angle X-ray scattering studies.

118 igins of stabilization by crowder molecules, small angle X-ray scattering was used to measure the fol

119 of ssDNA conformations in solution, we pair small angle X-ray scattering with novel ensemble fitting

120 we have studied Gpc1 using crystallography, small angle x-ray scattering, and chromatographic approa

121 th factor complex using electron microscopy, small angle x-ray scattering, and circular dichroism spe

122 from a combination of X-ray crystallography, small angle X-ray scattering, and complementary biophysi

123 e show using analytical ultracentrifugation, small angle x-ray scattering, and enzyme kinetic analyse

124 Our crystallographic, small angle x-ray scattering, and NMR analysis revealed

125 ion of the oligomeric state in solution with small angle x-ray scattering, and the spectrophotometric

126 m70 interaction, which has been validated by small angle x-ray scattering, hydrogen/deuterium exchang

127 using an integrative approach that combines small angle X-ray scattering, NMR spectroscopy, and mole

128 We also studied the complex in solution by small angle X-Ray scattering, nuclear magnetic resonance

129 ination of biophysical techniques, including small angle x-ray scattering, single particle electron m

130 Using small angle x-ray scattering, we show that isolated bull

131 The small angle x-ray scattering-derived models suggest a di

132 the full-length PexRD54-ATG8CL complex using small angle x-ray scattering.

133 ted by the custom ligands and verified using small angle x-ray spectroscopy, allows us to calculate t

134 Here, we use small- angle x-ray scattering with a spot size in the mi

135 ts, including size exclusion chromatography, small-angle x ray scattering, and circular dichroism spe

136 Here, small-angle X-ray and neutron scattering are applied to

137 sed for (cryo-) electron microscopy (EM) and small-angle X-ray and neutron-scattering studies.

138 Time-resolved small-angle X-ray diffraction measurements of WT twitchi

139 Here we show by synchrotron small-angle X-ray diffraction of frog (Rana temporaria)

140 Using synchrotron small-angle X-ray diffraction to probe time-dependent ch

141 Here, we used grazing-incidence small-angle X-ray scattering (GISAXS) to quantify nuclea

142 ensemble of scanning transmission microbeam small-angle X-ray scattering (muSAXS) patterns.

143 Small-angle X-ray scattering (SAXS) also indicates that

144 Crystallographic and small-angle X-ray scattering (SAXS) analyses indicate th

145 However, small-angle X-ray scattering (SAXS) analysis of WT FrdA

146 tructure of the passenger domain obtained by small-angle X-ray scattering (SAXS) analysis.

147 Using small-angle X-ray scattering (SAXS) and a quantitative f

148 We determined small-angle X-ray scattering (SAXS) and crystal structur

149 Using small-angle X-ray scattering (SAXS) and electron microsc

150 ssembly via hydrogen bonding is detailed via small-angle X-ray scattering (SAXS) and electrospray ion

151 In this work, we propose the combination of small-angle X-ray scattering (SAXS) and high throughput,

152 spectroscopy (FCS) experiments combined with small-angle X-ray scattering (SAXS) and viscosity measur

153 traumatic fracture states using synchrotron small-angle x-ray scattering (SAXS) at low and high stra

154 Small-angle X-ray scattering (SAXS) confirms that this t

155 This prior was then refined against small-angle X-ray scattering (SAXS) data employing an es

156 truction of homo-multimers, consideration of small-angle X-ray scattering (SAXS) data, and location o

157 ng a protein's flexibility in solution using small-angle X-ray scattering (SAXS) data.

158 The Small-Angle X-ray Scattering (SAXS) envelope of PECAM-1

159 escence resonance energy transfer (FRET) and small-angle X-ray scattering (SAXS) experiments disagree

160 g and the shape of the dimerization curve in small-angle X-ray scattering (SAXS) experiments using is

161 hoton-correlation spectroscopy (XPCS) in the small-angle X-ray scattering (SAXS) geometry to probe bo

162 Thus, small-angle x-ray scattering (SAXS) has been used for st

163 ant concentration, but several studies using small-angle X-ray scattering (SAXS) have reported no suc

164 Small-angle x-ray scattering (SAXS) is uniquely sensitiv

165 Small-angle X-ray scattering (SAXS) measurements reveal

166 tion temperature (TODT = 66 degrees C) using small-angle X-ray scattering (SAXS) measurements.

167 Small-angle X-ray scattering (SAXS) showed a maximum par

168 NMR and small-angle X-ray scattering (SAXS) structural analyses

169 Mutational and small-angle X-ray scattering (SAXS) studies confirm the

170 tion with denaturant concentration, but most small-angle X-ray scattering (SAXS) studies found no cha

171 We demonstrate by small-angle X-ray scattering (SAXS) that HMBPP binding t

172 n-state NMR, small-angle neutron scattering, small-angle X-ray scattering (SAXS), and Forster resonan

173 zed by 2D diffusion NMR spectroscopy (DOSY), small-angle X-ray scattering (SAXS), and molecular model

174 f unfolded proteins, NMR spectroscopy (NMR), small-angle X-ray scattering (SAXS), and single-molecule

175 Using small-angle X-ray scattering (SAXS), crystalline domain

176 Solution small-angle X-ray scattering (SAXS), electron microscopy

177 thium storage mechanism are also revealed by small-angle X-ray scattering (SAXS), especially the clos

178 icles, incorporating structure modeling with small-angle X-ray scattering (SAXS), pair distribution f

179 Furthermore, using small-angle X-ray scattering (SAXS), the positions of th

180 ine learning results with killing assays and small-angle X-ray scattering (SAXS), we find that the SV

181 By combining NMR with mutagenesis and small-angle X-ray scattering (SAXS), we show that these

182 uorescence resonance energy transfer (FRET), small-angle x-ray scattering (SAXS), x-ray crystallograp

183 isothermal titration calorimetry (ITC), and small-angle X-ray scattering (SAXS).

184 divalent ions, consistent with results from small-angle X-ray scattering (SAXS).

185 radius of gyration (RG ), can be measured by small-angle X-ray scattering (SAXS).

186 Through interpretation of ultra-small-angle X-ray scattering (USAXS) patterns of MF usin

187 in situ tandem X-ray absorption spectroscopy-small-angle X-ray scattering (XAS-SAXS).

188 Microfocus small-angle X-ray scattering allows us to monitor the fi

189 Here, we report crystallographic and small-angle X-ray scattering analyses of Norrin in compl

190 Moreover, an APE2 Zf-GRF X-ray structure and small-angle X-ray scattering analyses show that the Zf-G

191 imer in the presence of NEIL1 and DNA, while small-angle X-ray scattering analysis confirmed the NEIL

192 into electron density envelopes generated by small-angle x-ray scattering analysis of catalytically i

193 orm, and inverse-tapered molecular "shapes." Small-angle X-ray scattering analysis of the self-assemb

194 Small-angle X-ray scattering analysis revealed that upon

195 Using small-angle X-ray scattering and a fluorescence-based as

196 Characterization by small-angle X-ray scattering and atomic force microscopy

197 beta-lactoglobulin (betaLG), were studied by small-angle x-ray scattering and both near- and far-UV c

198 lO4 was studied by in situ grazing-incidence small-angle X-ray scattering and complementary scanning

199 Utilizing small-angle X-ray scattering and cryoelectron microscopy

200 lar organic framework (MSOF) is confirmed by small-angle X-ray scattering and diffraction experiments

201 Finally, small-angle X-ray scattering and dynamic light scatterin

202 Small-angle X-ray scattering and multi-angle laser light

203 d unphosphorylated rOPN were investigated by small-angle x-ray scattering and no significant changes

204 The determined ensemble was supported by small-angle x-ray scattering and nuclear magnetic resona

205 Using small-angle x-ray scattering and osmotic stress methods,

206 ion are analysed by simultaneous synchrotron small-angle X-ray scattering and Raman spectroscopy in a

207 We combine time-resolved (TR) small-angle X-ray scattering and TR-FRET to correlate ch

208 e structurally analyzed via a combination of small-angle X-ray scattering and, when appropriate, elec

209 We were able to perform small-angle x-ray scattering at sufficiently low daptomy

210 led to experimental assays such as anomalous small-angle x-ray scattering can provide important insig

211 eraction fraction obtained with the proposed small-angle X-ray scattering characterization method exh

212 Solution small-angle X-ray scattering combined with ensemble opti

213 As demonstrated by small-angle x-ray scattering comparative analysis of wil

214 between simulated and experimental anomalous small-angle x-ray scattering curves, demonstrating that

215 ar weight of the complex was calculated from small-angle X-ray scattering data and was in good agreem

216 The structure was accurately modeled from small-angle x-ray scattering data by treating ColN as a

217 tetramers and one homopentamer) had solution small-angle X-ray scattering data consistent with the de

218 Combining these results with small-angle X-ray scattering data for the complex of TRN

219 copy, Forster resonance energy transfer, and small-angle x-ray scattering data obtained under conditi

220 Experimental and simulated small-angle X-ray scattering data of Bi@U24 and Pb@U24 s

221 Small-angle X-ray scattering data revealed excellent agr

222 Small-angle X-ray scattering data show that Rho preferen

223 of the double-tetrameric form, combined with small-angle X-ray scattering data, allows the localisati

224 ate the RNA secondary structure information, small-angle X-ray scattering data, and any readily avail

225 information with integrative modeling using small-angle X-ray scattering data.

226 ar envelope for the P-CR domain derived from small-angle X-ray scattering data.

227 Small-angle x-ray scattering done in the presence of TEG

228 Small-angle x-ray scattering experiments conducted with

229 Small-angle x-ray scattering experiments on lens tissue

230 tion and shape is often determined either by small-angle x-ray scattering experiments or pulsed-field

231 Complementary small-angle X-ray scattering experiments reveal a strong

232 Molecular dynamics simulations and small-angle X-ray scattering experiments support this no

233 oosely associated" homodimer as indicated by small-angle x-ray scattering experiments.

234 rolysis transition-state mimic), and ADP via small-angle x-ray scattering has revealed a peristaltic

235 P2 structure by X-ray crystallography and by small-angle X-ray scattering in solution as well as that

236 Time-resolved small-angle X-ray scattering is applied to monitor the s

237 Small-angle X-ray scattering is used to study the struct

238 Dynamic light scattering and small-angle X-ray scattering lend important insights int

239 ty (self-interactions) of IDPs from a single small-angle x-ray scattering measurement.

240 of crystallization by in situ time-dependent small-angle X-ray scattering measurements.

241 l structure of full-length KGA and present a small-angle X-ray scattering model for full-length GLS2.

242 e modeled into a previously determined CesA8 small-angle X-ray scattering molecular envelope to produ

243 structures of two forms of human C-Ala, and small-angle X-ray scattering of AlaRS, showed that the l

244 Furthermore, structural information from small-angle X-ray scattering of LHn/D is compared among

245 ing analytical ultracentrifugation, NMR, and small-angle x-ray scattering on full-length ColN and its

246 n alternative interpretation of experimental small-angle X-ray scattering profiles of these systems,

247 Here, we report biochemical data, small-angle X-ray scattering results, negative-stain ele

248 c solution structure of BH0236 determined by small-angle X-ray scattering revealed structural insight

249 does not bind to the DUF Rossmann fold, and small-angle X-ray scattering reveals a novel dimer that

250 Small-angle X-ray scattering showed that certain sequenc

251 Here, supported by a small-angle x-ray scattering solution study of human NGF

252 Small-angle X-ray scattering studies of linker mutants r

253 Through small-angle X-ray scattering studies of sTie2 dimers in

254 Small-angle X-ray scattering studies reveal that this co

255 Small-angle x-ray scattering studies revealed that HMGA2

256 is work, we have investigated by in-solution small-angle x-ray scattering the structural and thermody

257 tures of individual VSG domains, we employed small-angle X-ray scattering to elucidate the first two

258 ements, atomic force microscopy imaging, and small-angle x-ray scattering to show that the structure

259 computational models were compared with the small-angle x-ray scattering trimer profile to explore t

260 Small-angle X-ray scattering was employed for the determ

261 Small-angle X-ray scattering was used to demonstrate tha

262 es that can be studied by x-ray diffraction (small-angle x-ray scattering).

263 NMR and SAXS (small-angle X-ray scattering)/WAXS (wide-angle X-ray sca

264 Here, we used NMR spectroscopy, mutagenesis, small-angle X-ray scattering, and computational modeling

265 t scattering, size exclusion chromatography, small-angle x-ray scattering, and enzyme kinetics.

266 at multiple time scales using solution NMR, small-angle X-ray scattering, and molecular dynamics sim

267 d and unbound state using mass spectrometry, small-angle X-ray scattering, and negative-stain electro

268 Electron microscopy, small-angle x-ray scattering, and x-ray crystallography

269 V039 using isothermal titration calorimetry, small-angle X-ray scattering, and X-ray crystallography.

270 ly of the bottlebrushes was characterized by small-angle X-ray scattering, atomic force microscopy, a

271 at provide distributions of species, such as small-angle X-ray scattering, electron microscopy, and a

272 By size exclusion chromatography and small-angle X-ray scattering, Gag in solution appears ex

273 By using small-angle x-ray scattering, high-resolution NMR spectr

274 Using X-ray crystallography, small-angle X-ray scattering, hydrogen-deuterium exchang

275 on GAPDH oligomerization by crystallography, small-angle x-ray scattering, nano-electrospray ionizati

276 n overlapping fragments of the receptor with small-angle X-ray scattering, native mass spectrometry a

277 Small-angle X-ray scattering, NMR and RNA-binding analys

278 Using small-angle X-ray scattering, precipitation rates of (Fe

279 t (PRE) distance restraints, dihedral angle, small-angle X-ray scattering, residual dipolar coupling

280 the cellular data, biophysical measurements (small-angle X-ray scattering, single-molecule fluorescen

281 Using in situ small-angle X-ray scattering, we observe continuous grow

282 , using truly in situ and fast time-resolved small-angle X-ray scattering, we quantify the four-stage

283 scopy, isothermal titration calorimetry, and small-angle X-ray scattering, we show that in the homodi

284 g cryo-electron microscopy and time-resolved small-angle X-ray scattering, we show that lipopolysacch

285 Using small-angle X-ray scattering, we unexpectedly found diff

286 Our small-angle x-ray scattering-based tetrameric model of S

287 ployed in-line size exclusion chromatography-small-angle X-ray scattering.

288 ectron microscopy, oscillatory rheology, and small-angle X-ray scattering.

289 ng both transmission electron microscopy and small-angle x-ray scattering.

290 th mass spectrometry, negative-stain EM, and small-angle X-ray scattering.

291 optical microscopy, infrared microscopy, and small-angle X-ray scattering.

292 ied using small-angle neutron scattering and small-angle x-ray scattering.

293 e DBLbeta3_D4::24E9 Fab complex derived from small-angle x-ray scattering.

294 a structural model of the complex scored by small-angle X-ray scattering.

295 M, cross-linking mass spectrometry, NMR, and small-angle X-ray scattering.

296 at the ensemble level using solution NMR and small-angle x-ray scattering.

297 roMPO and its solution structure obtained by small-angle X-ray scattering.

298 that of its complex with a tRNA precursor by small-angle X-ray scattering.

299 port a 2.1-A crystal structure of Nop9 and a small-angle X-ray-scattering model of a Nop9:RNA complex

300 uring the attenuation, refraction and (ultra-small-angle) X-ray scattering, does not have coherence r