ライフサイエンスコーパス: SAXS

1 SAXS analysis combined with molecular modeling simulatio

2 SAXS analysis indicates the ferrihydrite particles have

3 SAXS and H/D exchange data showed that global tertiary s

4 SAXS and mutational analyses further reveal that the pre

5 SAXS can bridge these information gaps by providing a re

6 SAXS data are complemented by NMR measurements and poten

7 SAXS data are consistent with atomic-resolution structur

8 SAXS data suggest structural flexibility in EF hand doma

9 SAXS data suggested a global shape of a hollow elliptica

10 SAXS data support a model in which the linker is flexibl

11 SAXS data were analyzed with a to our knowledge new deco

12 SAXS data, on the other hand, reveal the formation of an

13 SAXS experiments measure molecules in solution, without

14 SAXS experiments on 5.2, 13.3, and 13.8 nm hollow-shell

15 SAXS in combination with cryo-TEM confirms this unusuall

16 SAXS is thus an attractive alternative when crystallogra

17 SAXS measurements on bulk crystalline samples reveal tha

18 SAXS measurements show that the reaction intermediate fo

19 SAXS showed evidence of changes in betaG but not AX in t

20 SAXS solution structures of SNX20 and SNX21 show that th

21 SAXS studies further show compaction of the protein upon

22 SAXS studies indicate that, on average, three worms are

23 SAXS was used to study the interactions between the prot

24 SAXS, NMR, and ESI MS differentiate beta-NaSn13 , Sn12 ,

25 SAXS, UV/vis, and NMR spectroscopic techniques confirm t

26 SAXS-derived numerical estimates of dimensional paramete

27 A SAXS experiment determines the scattering intensity of a

28 al models for the interacting partners and a SAXS curve.

29 S (Fast X-Ray Scattering) rapidly computes a SAXS profile of a given atomistic model and fits it to a

30 ocks two rigid protein structures based on a SAXS profile of their complex.

31 rom a single input structure by fitting to a SAXS profile of the protein in solution.

32 dration layer model was also compared with a SAXS profile calculated for the explicit water molecules

33 eotide steps and refining the models against SAXS data, a broad array of structures can be obtained t

34 all-atom coordinates for refinement against SAXS data using the Xplor-NIH program.

35 r for protein-protein docking filtered by an SAXS profile, the SAXS Merge server for automatic mergin

36 redicting a structural ensemble that fits an SAXS profile, the FoXSDock server for protein-protein do

37 h the feasibility of obtaining the analogous SAXS parameter, I(0,0,0), experimentally.

38 Small angle X-ray scattering analysis (SAXS) supports the existence of both crystal structures

39 Our CEST and SAXS experiments, at different magnesium ion concentrati

40 Size-exclusion chromatography and SAXS experiments reveal that the isolated R.CglI, R.NgoA

41 Both DLS and SAXS studies indicate minimal change in the overall vesi

42 By computing FRET efficiencies and SAXS intensities at each denaturant concentration, we sh

43 Single-molecule FRET and SAXS demonstrate that only the open-form is capable of b

44 me conformation and stability using FRET and SAXS.

45 Furthermore, homology modeling and SAXS allowed the construction of a model that explains t

46 By mutagenesis and SAXS, we show that pUb binds to RING1 of Parkin at a sit

47 NMR and SAXS (small-angle X-ray scattering)/WAXS (wide-angle X-r

48 r that complex from a combination of NMR and SAXS data.

49 Finally, by NMR and SAXS experiments, we show that the tau molecules must be

50 sing the program X-PLOR-NIH based on NMR and SAXS restraints agree remarkably well; even the shapes o

51 solution structural information from NMR and SAXS suggests that the structures of the cold-induced an

52 roscopic (UV-vis, CD, fluorescence, NMR, and SAXS) and microscopic studies (TEM and AFM) showed that

53 Multi-angle light scattering and SAXS demonstrate that YabA is a tetramer in which the CT

54 f trASADH was confirmed by sedimentation and SAXS experiments.

55 RNA SHAPE and SAXS data were used to help model the extended (Tat Argi

56 Molecular dynamics simulations and SAXS demonstrate a dynamic equilibrium between open and

57 and unlabeled polypeptides using smFRET and SAXS, we directly assessed the contributions of dyes to

58 a three-armed shape, as revealed by TEM and SAXS analyses.

59 ating to 150 degrees C, as judged by TEM and SAXS.

60 NA and with an antibody fragment, as well as SAXS and domain association studies in solution.

61 ER was applied to the proteins of asymmetric SAXS profile distributions, the average TM-score of the

62 Because SAXS analyses often require comparing profiles calculate

63 lts thus argue that the disagreement between SAXS and smFRET is statistically significant and that th

64 Finally, both SAXS and SCMFT indicate a significant degree of solvent

65 lustrate this self-consistency, we used both SAXS and FRET data in a Bayesian procedure to refine str

66 g (DLS) techniques in the case of LDL and by SAXS, DLS, and Z-scan (ZS) techniques in the case of HDL

67 ed of ca. 50 POMs that were characterized by SAXS and transmission electron microscopy (TEM).

68 s into the vesicle membrane, as confirmed by SAXS analysis.

69 P1 crystal structure is further confirmed by SAXS and TEM data.

70 confirmed the C-shaped structure revealed by SAXS.

71 g water, and this can be followed in situ by SAXS.

72 An EM structure, supported by SAXS and crosslinking, reveals the architecture of the d

73 at require rapidly and accurately calculated SAXS profiles.

74 rms this unusually high degree of order (chi(SAXS) = 82%) and shows the nanoparticles to possess a ve

75 strates the applicability of chromatographic SAXS when studying biomolecules predisposed to aggregati

76 ombination of size exclusion chromatography, SAXS, and refractometry, we have determined a precise ge

77 ormations, a traditional single-conformation SAXS analysis is inappropriate, so we also discuss recen

78 irst demonstration of chromatography-coupled SAXS with Evolving Factor Analysis (EFA), a powerful met

79 Cryo-SAXS will thus enable structure determination of difficu

80 By combination of X-ray crystallography, SAXS and EM, together with biochemical evidences, here w

81 ring function and their capacity to describe SAXS data.

82 ely agree with the experimentally determined SAXS curves supporting the view that liraglutide forms h

83 Small- and wide-angle x-ray diffraction (SAXS and WAXS), as well as differential scanning calorim

84 g optical microscopy, and X-ray diffraction (SAXS, WAXS) regarding their mesomorphic properties.

85 lamellar nanostructures, as revealed by DSC, SAXS, and AFM, were generated.

86 for the self-segregation is provided by DSC, SAXS, WAXS, and TEM studies; in two of the samples, the

87 topological structures from an experimental SAXS profile are currently under active development.

88 , and we present current methods that extend SAXS data analysis to the super-resolution regime.

89 e Zernike polynomials-based method, and Fast-SAXS-pro.

90 Fitting SAXS patterns to a vesicle model enables calculation of

91 was investigated by static and stopped-flow SAXS measurements, revealing dynamic structural changes

92 a series of procedures that can be used for SAXS data collection and basic cross-checks designed to

93 pled with small-angle x-ray scattering (FPLC-SAXS) procedure.

94 le Forster resonance energy transfer (FRET), SAXS, dynamic light scattering (DLS), and two-focus fluo

95 data, such as several NMR observables, FRET, SAXS and cryo-electron microscopy data, and enables mode

96 l uncertainties of the Rg data measured from SAXS experiments, which suggest no compaction, leading t

97 The ensemble optimization method SAXS analysis demonstrates that the apo and Mg(2+)-bound

98 Moreover, SAXS models of the C-terminal globular regions of the al

99 ted its capsid-binding properties using NMR, SAXS, cryoEM and SPR.

100 Here we describe an efficient NMR-SAXS/WAXS approach for structural investigation of multi

101 Detailed analysis of SAXS curves indicated that the mean number of membranes

102 mpared with the S state based on analysis of SAXS data.

103 n damage currently limits the application of SAXS to molecules that can be produced in microgram quan

104 ) measured using the powerful combination of SAXS and smFRET.

105 are addressed, as well as the combination of SAXS with other X-ray and non-X-ray characterization too

106 Comparison of SAXS curves at high and low salt concentration shows tha

107 igh concentrations and averaging features of SAXS.

108 However, the interpretation of SAXS profiles is nontrivial because of the difficulty in

109 e SAXS Merge server for automatic merging of SAXS profiles and the Pose & Rank server for scoring pro

110 structural methods, illustrating the role of SAXS in structure refinement with NMR and ensemble refin

111 Here, we present a coherent synthesis of SAXS theory and experiment with a focus on analytical to

112 Herein we demonstrate the use of SAXS (small-angle X-ray scattering) to identify structur

113 Nevertheless, the use of SAXS and X-ray crystallography together to inspect PAH s

114 Moreover, advanced use of SAXS can provide unique insight into biomolecular behavi

115 Herein, we focus on the use of SAXS to examine nanoscale particulate systems.

116 ools will ultimately posit the usefulness of SAXS data beyond a simple space-filling approach by prov

117 vers for modeling atomic structures based on SAXS profiles.

118 ll and wide-angle X-ray scattering patterns (SAXS/WAXS) over 10 decades of time spanning from 100 ps

119 Perceived SAXS limitations are considered in light of its origins,

120 Based on the presented SAXS analysis it is found that the N-terminal domains of

121 High-quality SAXS data were collected for full-length recombinant mou

122 w is synchronized with synchrotron radiation SAXS measurements to probe protein interactions while mi

123 Small-angle scattering of x-rays (SAXS) and neutrons (SANS) are particularly useful and co

124 Here, current and recent SAXS-driven developments are described, with an emphasis

125 Here we report SAXS measurements on a 64 kDa bacterial group I ribozyme

126 gh limited to approximately 10 A resolution, SAXS can provide a wealth of structural information on b

127 Time resolved SAXS studies showed the abdomen to be the best site of i

128 n at small angles and in situ rheology (rheo-SAXS) experiments using the high X-ray flux of a synchro

129 trimeric nature from small angle scattering (SAXS) data.

130 Synchrotron small/wide angle scattering (SAXS/WAXS) images from three typical crystallographic pr

131 ing Small Angle X-ray or Neutron Scattering (SAXS or SANS), it is possible to follow in situ the form

132 Small-angle X-ray scattering (SAXS) also indicates that the cortactin repeats are intr

133 llographic and small-angle X-ray scattering (SAXS) analyses indicate that lattice symmetries and dime

134 We report small-angle X-ray scattering (SAXS) analyses of a whole module and a bimodule from DEB

135 Small-angle X-ray scattering (SAXS) analysis confirms the flexibility and dynamic natu

136 tion (PDF) and small-angle X-ray scattering (SAXS) analysis for a series of Fe fluorides, oxyfluoride

137 However, small-angle X-ray scattering (SAXS) analysis of WT FrdA cross-linked to SdhE suggested

138 Small angle X-ray scattering (SAXS) analysis revealed that IDE exists as a mixture of

139 Small-angle X-ray scattering (SAXS) analysis revealed that more exotic oligolamellar v

140 gestion and by small angle x-ray scattering (SAXS) analysis.

141 in obtained by small-angle X-ray scattering (SAXS) analysis.

142 Using small-angle X-ray scattering (SAXS) and a quantitative functional assay, we have now a

143 have utilized small angle x-ray scattering (SAXS) and biochemical techniques to characterize interac

144 combined with small angle X-ray scattering (SAXS) and confocal laser scanning microscopy (CLSM) stud

145 In this study, small-angle X-ray scattering (SAXS) and cryogenic transmission electron microscopy (cr

146 We determined small-angle X-ray scattering (SAXS) and crystal structures of the main ERQC enzyme, ER

147 ere studied by small-angle x-ray scattering (SAXS) and dynamic light scattering (DLS) techniques in t

148 Using small-angle X-ray scattering (SAXS) and electron microscopy averaging, we found that B

149 s detailed via small-angle X-ray scattering (SAXS) and electrospray ionization mass spectrometry (ESI

150 tures by using small angle x-ray scattering (SAXS) and equilibrium (45)Ca(2+) binding assays.

151 combination of small-angle X-ray scattering (SAXS) and high throughput, droplet based microfluidics a

152 solution-based small-angle x-ray scattering (SAXS) and molecular constrained data modeling, we show t

153 s suggested by small-angle x-ray scattering (SAXS) and multiangle static light scattering (MALS) resu

154 Here, small angle X-ray scattering (SAXS) and mutational analyses show APLF is largely an in

155 as verified by Small angle X-ray scattering (SAXS) and Transmission electron microscopy (TEM) and hol

156 combined with small-angle X-ray scattering (SAXS) and viscosity measurements for three proteins, alp

157 surements from small-angle X-ray scattering (SAXS) are highly informative to determine the structures

158 A small-angle X-ray scattering (SAXS) assay and other structural methods assessed aggreg

159 ng synchrotron small-angle x-ray scattering (SAXS) at low and high strain rates.

160 Small-angle X-ray scattering (SAXS) confirms that this tetramer, which dominates in th

161 Small angle X-ray scattering (SAXS) confirms the disruption of the PCNA trimer upon ad

162 pe measured by small-angle X-ray scattering (SAXS) confirms the STEM and PDF analysis.

163 efined against small-angle X-ray scattering (SAXS) data employing an established method (EROS).

164 N), along with small-angle X-ray scattering (SAXS) data for Munc18a bound to Syx1a, Syx1aDeltaN, and

165 agments to the small angle X-ray scattering (SAXS) data revealed that the protein's C-terminal domain

166 MR spectra and small-angle X-ray scattering (SAXS) data show that this beta-strand-rich conformation

167 nsideration of small-angle X-ray scattering (SAXS) data, and location of heparin-binding sites.

168 We compared small angle x-ray scattering (SAXS) data-based models and limited proteolysis profiles

169 s supported by small-angle X-ray scattering (SAXS) data.

170 solution using small-angle X-ray scattering (SAXS) data.

171 The Small-Angle X-ray Scattering (SAXS) envelope of PECAM-1 IgL1-6 supported such a dimer

172 fer (FRET) and small-angle X-ray scattering (SAXS) experiments disagree on whether Protein L collapse

173 ation curve in small-angle X-ray scattering (SAXS) experiments using isolated GluA2 ligand-binding do

174 (XPCS) in the small-angle X-ray scattering (SAXS) geometry to probe both the structural and dynamica

175 otron sources, small-angle X-ray scattering (SAXS) has become much more accessible to the structural

176 Thus, small-angle x-ray scattering (SAXS) has been used for studying the structures of compl

177 studies using small-angle X-ray scattering (SAXS) have reported no such increase of the radius of gy

178 ng synchrotron small-angle X-ray scattering (SAXS) in combination with the stopped-flow mixing techni

179 Small-angle X-ray scattering (SAXS) is a robust technique for the comprehensive struct

180 Small angle x-ray scattering (SAXS) is a versatile and widely used technique for obtai

181 Small Angle X-ray Scattering (SAXS) is an increasingly common and useful technique for

182 Small-angle x-ray scattering (SAXS) is uniquely sensitive to the spatial correlations

183 Small angle X-ray scattering (SAXS) is used to confirm silica encapsulation, since a s

184 Small angle x-ray scattering (SAXS) measurements and chemical cross-linking revealed t

185 Small-angle X-ray scattering (SAXS) measurements over a similar time range show that t

186 Small-angle X-ray scattering (SAXS) measurements reveal a striking difference in inter

187 grees C) using small-angle X-ray scattering (SAXS) measurements.

188 al probing and small angle x-ray scattering (SAXS) measurements.

189 Small angle X-ray scattering (SAXS) of solutions of Rb1 and Cs1 in varying conditions

190 A small angle X-ray scattering (SAXS) pattern shows the periodic packing of the ultrathi

191 techniques: a small-angle X-ray scattering (SAXS) profile, 2D class average images from negative-sta

192 low-resolution small angle X-ray scattering (SAXS) results show that the N-terminal extensions protru

193 Small angle X-ray scattering (SAXS) revealed no fixed orientation of the CTD with resp

194 Small angle X-ray scattering (SAXS) reveals a flexible multi-state complex that sugges

195 SHAPE-Seq and small-angle X-ray scattering (SAXS) reveals two major steps of Rev-RRE complex formati

196 Small-angle X-ray scattering (SAXS) showed a maximum particle dimension of 95 A with a

197 Interestingly small-angle X-ray scattering (SAXS) shows that these fibers of 5.6 nm cross-sectional

198 NMR and small-angle X-ray scattering (SAXS) structural analyses allowed us to construct models

199 he crystal and small-angle X-ray scattering (SAXS) structures of Bcl-xL treated with the mild deterge

200 Mutational and small-angle X-ray scattering (SAXS) studies confirm the structural similarities of TAP

201 tion, but most small-angle X-ray scattering (SAXS) studies found no change.

202 ound, solution small-angle X-ray scattering (SAXS) studies of the full-length enzyme, the characteriz

203 ion (XRD), and small-angle X-ray scattering (SAXS) techniques are used to probe the composition insid

204 demonstrate by small-angle X-ray scattering (SAXS) that HMBPP binding to the internal domain of BTN3A

205 ectroscopy and small angle x-ray scattering (SAXS) to calculate the maximum occurrence (MO) of MMP-1

206 microscopy and small angle X-ray scattering (SAXS) to determine the ATP-bound structure of the intact

207 mbination with small angle X-ray scattering (SAXS) to determine the structure of the main immunoreact

208 llography with small angle x-ray scattering (SAXS) to elucidate the structure of the plakin domain of

209 In this study, small-angle x-ray scattering (SAXS) was used to characterize Z-alpha1AT polymers in so

210 Small-angle x-ray scattering (SAXS) was used to study the behavior of equine metmyoglo

211 Small-angle X-ray scattering (SAXS) was used to verify that this binary mixture approa

212 Using small angle x-ray scattering (SAXS) we show that the CAR(tcp):RXR(9c).SRC1 complex can

213 We combine small angle X-ray scattering (SAXS) with ensemble-optimization methods (EOM) to dynami

214 ne proteins by small-angle X-ray scattering (SAXS), a technique frequently used to monitor conformati

215 spectroscopy, small-angle x-ray scattering (SAXS), and differential scanning calorimetry.

216 on scattering, small-angle X-ray scattering (SAXS), and Forster resonance energy transfer (FRET), we

217 oscopy (DOSY), small-angle X-ray scattering (SAXS), and molecular modeling.

218 roscopy (NMR), small-angle X-ray scattering (SAXS), and single-molecule Forster resonance energy tran

219 time-resolved small angle X-ray scattering (SAXS), and time-resolved negative stain electron microsc

220 iques, such as small-angle X-ray scattering (SAXS), can be applied at larger scale, but they miss ato

221 spectroscopy, small-angle X-ray scattering (SAXS), chemical cross-linking, and enzymatic assays to e

222 Using small-angle X-ray scattering (SAXS), crystalline domain size, (i.e., thickness of MF-C

223 Solution small-angle X-ray scattering (SAXS), electron microscopy (EM), and biophysical analysi

224 Small angle X-ray scattering (SAXS), electrospray ionization charge detection mass spe

225 so revealed by small-angle X-ray scattering (SAXS), especially the closed pore effects on lithium-ion

226 combination of small angle X-ray scattering (SAXS), low-pressure N2 and CO2 adsorption (LPGA) and hig

227 ned X-ray crystallography, X-ray scattering (SAXS), modeling and biophysical approaches, with in vivo

228 modeling with small-angle X-ray scattering (SAXS), pair distribution function (PDF), and X-ray powde

229 rifugation and small-angle X-ray scattering (SAXS), revealing an elongated molecule with dimensions o

230 using combined small angle X-ray scattering (SAXS), small angle neutron scattering (SANS) and low-pre

231 ogies, such as Small Angle X-ray Scattering (SAXS), Small Angle Neutron Scattering (SANS), spectrosco

232 hermore, using small-angle X-ray scattering (SAXS), the positions of the flanking acyl carrier protei

233 aracterized by small-angle X-ray scattering (SAXS), using a model quantitatively describing fractal a

234 try (ITC), and small angle x-ray scattering (SAXS), we dissect binding and catalysis on multiple phos

235 ing assays and small-angle X-ray scattering (SAXS), we find that the SVM metric sigma correlates not

236 Using small-angle x-ray scattering (SAXS), we investigated the phase behavior of mesophases

237 utagenesis and small-angle X-ray scattering (SAXS), we show that these states involve aromatic residu

238 ansfer (FRET), small-angle x-ray scattering (SAXS), x-ray crystallography, electron microscopy, and t

239 combination of small angle X-ray scattering (SAXS), X-ray hydroxyl radical footprinting, circular dic

240 or proteins by small-angle X-ray scattering (SAXS)-a factor overlooked in current analyses in terms o

241 of Pcore with small angle x-ray scattering (SAXS)-based ensemble modeling of the full-length P prote

242 h results from small-angle X-ray scattering (SAXS).

243 , rheology and small angle X-ray scattering (SAXS).

244 be achieved by small angle x-ray scattering (SAXS).

245 s confirmed by small-angle X-ray scattering (SAXS).

246 itu, real-time small-angle X-ray scattering (SAXS).

247 be measured by small-angle X-ray scattering (SAXS).

248 try (ITC), and small-angle X-ray scattering (SAXS).

249 and studied by small angle x-ray scattering (SAXS).

250 (13)C NMR and small angle X-ray scattering (SAXS).

251 uorescence and small-angle X-ray scattering (SAXS)].

252 ntary small and wide angle X-ray scattering (SAXS, WAXS), respectively.

253 of small- and wide- angle X-ray scattering (SAXS/WAXS) during in situ repeated tensile loading to el

254 In situ SAXS measurements of NC-assembled supercrystal and lead

255 In situ SAXS measurements supported by ex situ TEM indicate that

256 Although several sophisticated SAXS/SANS programs have been developed recently, the imp

257 hy, nuclear magnetic resonance spectroscopy, SAXS and molecular dynamics calculations, we show that t

258 endent of age, disease and treatment status, SAXS revealed reduced fibril plasticity at high strain r

259 hrotron small-angle X-ray scattering (SEC-SY-SAXS).

260 at 37 degrees C, as revealed by synchrotron SAXS and TEM.

261 of Au on CdSe/CdS nanorods using synchrotron SAXS technique and time-resolved spectroscopy.

262 rties on the hydration shell by a systematic SAXS/SANS study using three mutants of a single protein,

263 Biophysical evidence from TEM, cryo-TEM, SAXS, AFM, and STEM measurements on the 3FD-IL nanosheet

264 e as a function of spatial frequency, termed SAXS profile.

265 The SAXS data capture the enzyme's quaternary structure and

266 The SAXS data for pure RL micelles can be described by prola

267 The SAXS data for SDS agree with oblate-shaped micelles with

268 The SAXS envelope of a truncated form of DrDps1 without the

269 The SAXS-derived models suggest that IcsA has an elongated s

270 Molecular modelling against the SAXS data suggested that the linker in H. pylori MotB fo

271 Also, the SAXS results did not indicate significant structural cha

272 y analytical ultracentrifugation confirm the SAXS model.

273 ess favorable lens shape required to fit the SAXS data from the N-terminal truncated nanodisc system

274 determination of radius of gyration from the SAXS experiments.

275 the dynamics in momentum space, which in the SAXS geometry reflects structural relaxation on the nano

276 g the elongated architecture observed in the SAXS structure.

277 gy models of the individual domains into the SAXS-derived molecular envelope.

278 Ab initio modeling of the SAXS data results in a long kinked structure of the tern

279 emonstrated a significant correlation of the SAXS score with the accuracy of a structural model.

280 of ensemble optimization, weighing in on the SAXS contributions of a heterogeneous mixture of conform

281 ein docking filtered by an SAXS profile, the SAXS Merge server for automatic merging of SAXS profiles

282 model provides satisfactory data fits to the SAXS patterns and allows the mean silica volume fraction

283 In agreement with the SAXS data, the heptamer forms a water-filled oligomer of

284 Theoretical SAXS curves extracted from the simulations qualitatively

285 Thus, SAXS provides an experimental constraint to guide or tes

286 synchrotron beamlines that are dedicated to SAXS are often unfamiliar to the nonspecialist.

287 me-resolved small angle X-ray scattering (TR-SAXS) to determine transient structures of protein and D

288 Six trimeric SAXS models nearly filled the space below an average FF-

289 Using SAXS data collected on an absolute intensity scale for s

290 Using SAXS we show that in solution the SR3-SR6 and SR7-SR9 re

291 Using SAXS, we further describe the domain movements involved

292 e of the NTR in solution was confirmed using SAXS.

293 ort factor RanBP5 that can be modelled using SAXS and we show that the PA-PB1-RanPB5 complex is no lo

294 This is the first case in which SAXS and FRET have yielded even qualitatively consistent

295 mbranes are produced for x = 200-1000, while SAXS indicates a gradual reduction in mean aggregation n

296 tions of the unbound RecU, in agreement with SAXS observations.

297 t protein liquid chromatography coupled with SAXS minimized data artifacts caused by a non-monodisper

298 Cryo-TEM, used together with SAXS to determine fibril dimensions, shows that the leng

299 mic-scale characterization techniques (XAFS, SAXS, XRF, and electron microscopy) to follow the proces

300 ectroscopy-small-angle X-ray scattering (XAS-SAXS).