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 analysis of a truncated RcRE variant revealed an "A

4 SAXS and biochemical analyses demonstrated that the "A"

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

6 SAXS and mutational analyses further reveal that the pre

7 SAXS data are complemented by NMR measurements and poten

8 SAXS data show that the complex retains features of the

9 SAXS data suggest structural flexibility in EF hand doma

10 SAXS data suggested a global shape of a hollow elliptica

11 SAXS measurements on bulk crystalline samples reveal tha

12 SAXS measurements show that the reaction intermediate fo

13 SAXS performed on AMP-PNP-DnaA (H136Q) indicates that th

14 SAXS results indicated that surface-modified nanoparticl

15 SAXS revealed increases in the native state radius of gy

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

17 SAXS shows that interbilayer spacing (D) in the cochleat

18 SAXS solution structures of SNX20 and SNX21 show that th

19 SAXS studies further show compaction of the protein upon

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

21 SAXS was used to study the interactions between the prot

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

23 A SAXS experiment determines the scattering intensity of a

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

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

26 tains normal activation by VWF D4, and has a SAXS envelope consistent with amputation of the hairpin

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

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

29 ng-state and activated forms of C29S against SAXS data with available structural data created and eva

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

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

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

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

34 Integrating x-ray crystallography and SAXS, we also describe the structure of the higher eukar

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

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

37 the results from earlier electrochemical and SAXS studies stating that the closed conformation, where

38 uding TEM, AFM, high-resolution cryo-EM, and SAXS/WAXS measurements, reveals that the sheet and tube

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

40 e tested the recent suggestion that FRET and SAXS results can be reconciled if the R(g) and R(ee) are

41 Furthermore, based on SEC-MALS and SAXS analyses of McrBC and the structure of McrB, we pro

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

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

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

45 ensembles were compared to available NMR and SAXS data for validation.

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

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

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

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

50 2D proton nuclear magnetic resonance and SAXS data provided constraints on the solution structure

51 Remarkably, TEM, rheology and SAXS studies indicate that a single copolymer compositio

52 he bilayer spacings (as observed by SANS and SAXS) on the ratio between amount of water and amphiphil

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 ve apparent discrepancies between smFRET and SAXS inferences, we integrated SAXS data with NMR data a

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

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

59 y using it to direct autonomous small-angle (SAXS) and grazing-incidence small-angle (GISAXS) x-ray s

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

61 nt conformational changes of ectoIRR in both SAXS and AFM experiments, an observation that agreed wel

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

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

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

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

66 of the microstructure of the gel network by SAXS at several scales (1-100 nm) were considered.

67 triking conformational change as observed by SAXS, implying that altering the hetero-domain interacti

68 confirmed the C-shaped structure revealed by SAXS.

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

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

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

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

73 d invite the application of time-resolved CV-SAXS to reveal interactions that result in efficient vir

74 t variation small-angle X-ray scattering (CV-SAXS) is a powerful tool with the potential to monitor t

75 ted MS2 RNA was exclusively detected with CV-SAXS and compared with a structure derived from asymmetr

76 ring function and their capacity to describe SAXS data.

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

78 ts indicate that as aids in tissue diagnosis SAXS is capable of distinguishing areas of invasion by d

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

80 s, excellent agreement with the experimental SAXS data, and a large-scale rearrangement of the signal

81 Fitting SAXS patterns to a vesicle model enables calculation of

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

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

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

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

86 structural ensemble previously derived from SAXS and NMR relaxation measurements.

87 (R(g)) and end-to-end distance (R(ee)) from SAXS profiles, we tested the recent suggestion that FRET

88 Structural information, gathered from SAXS and cryo-TEM, reveals that the distinct peptide dom

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

90 Further, SAXS analysis of the TmTsaB2D2-tRNA complex in solution

91 By harnessing recent advances in SAXS and FRET experiments and setting these findings in

92 en smFRET and SAXS inferences, we integrated SAXS data with NMR data and reserved the smFRET data for

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

94 NMR, SAXS, and molecular modeling demonstrate that LC8 bindin

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

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

97 g partner protein Brn1(Cnd2) The analysis of SAXS and dynamic and static multiangle light scattering

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

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

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

101 igh concentrations and averaging features of SAXS.

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

103 studied several back-calculation software of SAXS scattering intensity and optimized the adjustable p

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

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

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

107 vers for modeling atomic structures based on SAXS profiles.

108 were detected in all E172 samples by TEM or SAXS measurements.

109 Our SAXS-based model supports the notion that binding of JDB

110 We combine our SAXS and SANS experiments with molecular dynamics simula

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

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

113 teractions are sufficient to reconcile prior SAXS and FRET studies, thus providing a unified picture

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

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

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

117 Here, we report SAXS characterization of the condensin HEAT-repeat subun

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

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

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

121 roscopy, small-angle X-ray light scattering (SAXS), and molecular dynamics simulations, we provide he

122 hese proteins, small-angle X-ray scattering (SAXS) allows for a quantitative assessment and modeling

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

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

125 (cryo-EM) and small-angle X-ray scattering (SAXS) analyses of recombinant disulfide-linked dimeric M

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

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

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

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

130 Using small-angle X-ray scattering (SAXS) and atomic force microscopy (AFM), we investigated

131 solution using small-angle X-ray scattering (SAXS) and atomic force microscopy (AFM).

132 tron radiation small-angle X-ray scattering (SAXS) and circular dichroism (CD).

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

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

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

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

137 in solution by small-angle X-ray scattering (SAXS) and exploited the scattering profile in modeling o

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

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

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

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

142 reparation for Small-Angle X-Ray Scattering (SAXS) and Small-Angle Neutron Scattering (SANS) characte

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

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

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

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

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

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

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

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

151 However, small angle X-ray scattering (SAXS) data were used to assert the opposite, while inter

152 we use NMR and small-angle x-ray scattering (SAXS) data with multiple molecular dynamics (MD) simulat

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

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

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

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

157 Small-angle X-ray scattering (SAXS) experiments on JBP1 and JDBD in the presence or ab

158 microscopy and small-angle X-ray scattering (SAXS) experiments reveal the formation of four classes o

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

160 scattering and small-angle X-ray scattering (SAXS) experiments.

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

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

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

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

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

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

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

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

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

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

171 llography, and small-angle X-ray scattering (SAXS) methodologies to demonstrate that adenine/guanine

172 FRET data with small-angle X-ray scattering (SAXS) models and published crystal structures of isolate

173 Small-angle X-ray scattering (SAXS) models of BMAL1 and BMAL1:KIX complexes revealed t

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

175 procedure for small-angle X-ray scattering (SAXS) profiles and used it to demonstrate that even rela

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

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

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

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

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

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

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

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

184 In situ small-angle X-ray scattering (SAXS) studies of reversible addition-fragmentation chain

185 -based in-situ small angle X-ray scattering (SAXS) suggests that the sizes of the two samples and the

186 roteolysis and small-angle X-ray scattering (SAXS) support the proper folding of both the 14-3-3 and

187 ng synchrotron small angle x-ray scattering (SAXS) techniques, determining nanometer scale structural

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

189 We use small-angle X-ray scattering (SAXS) to characterize the structure of this carotenoprot

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

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

192 Here, we used Small Angle X-ray Scattering (SAXS) to investigate oligomerization of DnaA in solution

193 By small angle X-ray scattering (SAXS) we have demontrated how the self-assembled structu

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

195 By small angle X-ray scattering (SAXS), ADAMTS13 adopts a hairpin-like conformation with

196 time-resolved small-angle X-ray scattering (SAXS), all-atom simulations, and polymer theory.

197 combined with small-angle X-ray scattering (SAXS), also allowed us to predict the general position o

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

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

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

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

202 spectroscopy, Small-angle X-ray Scattering (SAXS), and single-molecule Forster Resonance Energy Tran

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

204 combination of small-angle x-ray scattering (SAXS), atomistic molecular dynamic simulations, single-m

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

206 combination of small-angle X-ray scattering (SAXS), computational studies, mutagenesis and microbial

207 studies using small-angle X-ray scattering (SAXS), confirmed this conformational flexibility.

208 asurements and small-angle X-ray scattering (SAXS), coupled with biochemical and functional analyses

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

210 e strengths of small-angle X-ray scattering (SAXS), crystallography, and cryo-electron microscopy (cr

211 ility by using small-angle X-ray scattering (SAXS), dynamic light scattering (DLS), and NMR relaxatio

212 Small-Angle X-ray Scattering (SAXS), Dynamic Light Scattering (DLS), Transmission Elec

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

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

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

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

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

218 entrifugation, small-angle X-ray scattering (SAXS), molecular dynamics (MD) simulations, and ligand-b

219 e described by small-angle X-ray scattering (SAXS), pair distribution function (PDF), and electrospra

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

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

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

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

224 Using small angle X-ray scattering (SAXS), we elucidate the ensemble of Bvht RNA conformatio

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

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

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

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

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

230 Small angle X-ray scattering (SAXS)-based structural analysis of this protein indicate

231 e validated by small-angle X-ray scattering (SAXS).

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

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

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

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

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

237 as measured by small angle X-ray scattering (SAXS).

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

239 constructs by small-angle X-ray scattering (SAXS).

240 chrotron-based small angle x-ray scattering (SAXS).

241 time-resolved Small Angle X-ray Scattering (SAXS).

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

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

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

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

246 situ small- and wide-angle X-ray scattering (SAXS/WAXS), atomic force and cryogenic transmission elec

247 SEC-SAXS, SHAPE and hydroxyl-radical cleavage establish that

248 upled with small-angle X-ray scattering (SEC-SAXS) analysis, we investigated the ACMSD tetramer struc

249 coupled to small-angle X-ray scattering (SEC-SAXS) of this hybrid module bound to 1D10 provided furth

250 line with small-angle X-ray scattering (SEC-SAXS) to analyze the full-length hPAH solution structure

251 tially regulates ACMSD activity and that SEC-SAXS coupled with X-ray crystallography is a powerful to

252 udy the phase separation process via in situ SAXS experiments as well as ex situ electron microscopy,

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

254 However, conducting the analogous in situ SAXS studies during RAFT aqueous emulsion polymerization

255 new PISA formulation well-suited for in situ SAXS studies using a new reaction cell.

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

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

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

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

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

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

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

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

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

270 table parameters to accurately calculate the SAXS intensity from an atomic structure.

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

272 In a cutting-edge approach, we fitted the SAXS data to full MD simulations from the same condition

273 he ACMSD tetramer structure, and fitting the SAXS data with X-ray crystal structures of the monomeric

274 determination of radius of gyration from the SAXS experiments.

275 From the SAXS patterns, axial d-spacing and diffuse scattering in

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

277 g the elongated architecture observed in the SAXS structure.

278 gh-resolution KIX domain structures into the SAXS-derived envelopes suggested that the G-region emerg

279 agreement between the two experiments is the SAXS-FRET controversy.

280 At the same time, the SAXS data highlight the weakness of the secondary interf

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

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

283 Theoretical SAXS curves extracted from the simulations qualitatively

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

285 , homology modeling, and flexible fitting to SAXS data using molecular dynamics.

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

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

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

289 Using SAXS, we further describe the domain movements involved

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

291 First, using SAXS we show that fluorophores employed in FRET can cont

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

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

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

295 h four had a size median below 100 nm, while SAXS showed a size median below 100 nm for six evaluated

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).