ライフサイエンスコーパス: solid-state NMR

1 osquitoes was investigated in vivo using 13C solid-state NMR.

2 re we report high-resolution (17)O (I = 5/2) solid-state NMR spectra of the mixed-conducting solid ox

3 1D and 2D solid-state NMR, as well as XRD data on lithiated sample

4 Here, we present a proton-detected 4D solid-state NMR assignment procedure that is tailored fo

5 Additionally, solid-state NMR was used to demonstrate correlation betw

6 owder X-ray diffraction (SR-XRD), and (27)Al solid-state NMR.

7 Although highly consistent with all solid-state NMR observables, the ensembles of more than

8 Furthermore elemental analysis and solid state NMR were used to obtain the bulk characteris

9 also characterized by X-ray diffraction and solid state NMR spectroscopy.

10 as quantified, using neutron diffraction and solid state NMR.

11 olecular modeling, molecular simulation, and solid state NMR suggests that inversion of the symmetric

12 as studied by PXRD, TEM, EDX, EELS, AFM, and solid-state NMR spectroscopy, revealing a high level of

13 Biochemical and solid-state NMR measurements of the matrix and constitut

14 with electron microscopy, biochemistry, and solid-state NMR spectroscopy to define the chemical comp

15 etric differential scanning calorimetry, and solid-state NMR.

16 culture by a combination of chiroptical and solid-state NMR spectroscopies, microscopy, bioassays, a

17 haracterization by X-ray crystallography and solid-state NMR spectroscopy.

18 ouble electron-electron resonance (DEER) and solid-state NMR (ssNMR) spectroscopy to refine the struc

19 branes by combining electrophysiological and solid-state NMR experiments.

20 diffraction, hydrogen-deuterium exchange and solid-state NMR studies map the beta-forming region to a

21 Fourier transform infrared and solid-state NMR spectroscopic studies reveal a central b

22 lementary techniques, including infrared and solid-state NMR spectroscopies.

23 rmediate assemblies by isotope-edited IR and solid-state NMR reveals unexpected strand orientation in

24 According to IR and solid-state NMR, the methyl group remains intact, and do

25 s of degradation were analyzed by liquid and solid-state NMR.

26 udies using calorimetry and both liquid- and solid-state NMR reveal the interactions behind the in vi

27 Combining both liquid- and solid-state NMR, we demonstrate that structural rearrang

28 e, fluorescence anisotropy measurements, and solid-state NMR spectroscopy to study the influence of p

29 nformation from cryo-electron microscopy and solid-state NMR spectroscopy is combined in a single str

30 ssemble into semi-elliptical nanosheets, and solid-state NMR provides insight into the self-assembly

31 scopy structures, mechanical properties, and solid-state NMR structural information to build a molecu

32 al model by combining experimental X-ray and solid-state NMR with molecular dynamics (MD) simulations

33 and electron density map reconstruction, and solid-state NMR, all as a function of temperature and he

34 joint calculation with X-ray reflections and solid-state NMR restraints, into the lipid bilayer and p

35 all-atom molecular dynamics simulations and solid-state NMR further reveal that the CypA-binding pat

36 nation of molecular dynamics simulations and solid-state NMR shows that a higher propensity for backb

37 all-atom molecular dynamics simulations and solid-state NMR spectroscopy.

38 n of molecular dynamics (MD) simulations and solid-state NMR was used to present an atomistic model o

39 rface has been characterized by solution and solid-state NMR and biochemical techniques but never cry

40 ere determined using a combined solution and solid-state NMR approach.

41 pecificity, we used a hybrid of solution and solid-state NMR methods in lipid bilayers and bicelles.

42 analyzed with a combination of solution and solid-state NMR techniques, including dynamic nuclear po

43 main of the Het-s protein using solution and solid-state NMR, electron and atomic force microscopies,

44 -validated examples using both solution- and solid-state NMR data.

45 that combines the strengths of solution- and solid-state NMR to measure dipolar, chemical shift, and

46 lecular assemblies, using both solution- and solid-state NMR.

47 on by time-resolved optical spectroscopy and solid-state NMR.

48 taneous measurement of both liquid-state and solid-state NMR spectra as a function of time.

49 wder and fiber X-ray diffraction studies and solid-state NMR experiments.

50 Here, we describe how one can apply solid-state NMR, ranging from 1D chemical shift assignme

51 esent the X-ray crystal structure as well as solid-state NMR spectroscopy, electrophysiology, and MD

52 y improve spectral sensitivity in biological solid-state NMR (ssNMR), thus allowing the study of larg

53 (35/37)Cl and (79/81)Br solid-state NMR spectroscopy is applied to characterize

54 d the edge groups are formed as confirmed by solid state NMR spectroscopy.

55 ure, unobservable by XRD but demonstrated by solid state NMR studies.

56 rosomal cytochrome-P450 and cytochrome-b5 by solid-state NMR spectroscopy.

57 ersion between polymorphs at 24 degrees C by solid-state NMR, showing that the two-fold symmetric "ag

58 Extensive surface characterization by solid-state NMR spectroscopy, IR spectroscopy, cyclic vo

59 withSiO)Lu[CH(SiMe3)2]2] is characterized by solid-state NMR and EXAFS spectroscopy, which show that

60 e four catalysts were fully characterized by solid-state NMR, N2 physisorption, SEM, and TGA in order

61 uid-crystalline lipid bilayer environment by solid-state NMR spectroscopy.

62 in these surface inclusions was examined by solid-state NMR and X-ray powder diffraction.

63 on between Cu(+)/Cu(2+) and Abeta fibrils by solid-state NMR (SSNMR) and other spectroscopic methods.

64 structural analysis of wild-type fibrils by solid-state NMR suggests a molecular repeat unit compris

65 osphate- and carbohydrate-induced fibrils by solid-state NMR.

66 porcine aortic elastin exposed to glucose by solid-state NMR spectroscopic and relaxation methodologi

67 bution of beta-strand segments identified by solid-state NMR, we propose that the DUF583 domain adopt

68 study of inorganic crystalline materials by solid-state NMR spectroscopy is often complicated by the

69 tingly, Q(4) (nAl) Si speciation measured by solid-state NMR can only be modeled with a few combinati

70 r, as crystallization proceeds (monitored by solid-state NMR), the solution state becomes more dilute

71 )(benzene)(+). AlS(-) species, observable by solid-state NMR and XAS.

72 e, we show that such data can be obtained by solid-state NMR enhanced by dynamic nuclear polarization

73 zed at the molecular level, in particular by solid-state NMR, and their alkyne metathesis catalytic a

74 try of membrane-associated HAfp is probed by solid-state NMR.

75 ion-state NMR) and of a membrane protein (by solid-state NMR) were published in 2001 and 2011, respec

76 brils at physiological pH that were shown by solid-state NMR to be assemblies of a two-rung beta-sole

77 lycosyl diastereomers to NKA were studied by solid-state NMR (SSNMR), which revealed interactions of

78 It has been extensively studied by solid-state NMR and computational methods.

79 bes of the peptide AAAAAAK can be studied by solid-state NMR and IR spectroscopy.

80 Structural and computational studies by solid-state NMR spectroscopy, XAS, and periodic DFT meth

81 ay techniques (2D-WAXS and XRD) supported by solid-state NMR (SS-NMR) and atomic force microscopy (AF

82 organic material was studied both in toto by solid-state NMR spectroscopy of the powders and by gas c

83 cavities were investigated by 2D (1)H-(13)C solid state NMR on samples loaded with enriched (13)CO2,

84 A newly designed 3D (2)H-(13)C-(13)C solid-state NMR magic angle spinning (MAS) experiment is

85 ier transform IR (FT-IR) spectroscopy, (13)C solid-state NMR spectroscopy, and thermogravimetric anal

86 s using one and two dimensional {(1)H}-(13)C solid-state NMR spectroscopy.

87 , and proteins/peptides using advanced (13)C solid-state NMR techniques.

88 1), using differential scanning calorimetry, solid-state NMR, powder X-ray diffraction, and dielectri

89 The (19)F-(19)F CODEX solid-state NMR experiments performed with ALM in POPC l

90 Here the authors combine solid-state NMR measurements and molecular dynamics simu

91 Here we combine solid-state NMR and structural bioinformatics to determi

92 structural refinement approach that combines solid-state NMR experiments and molecular simulations to

93 We report nearly complete solid-state NMR (ssNMR) resonance assignments of Rous sa

94 Comparing DNP-enhanced and conventional solid-state NMR, an absolute sensitivity ratio of 24 was

95 f approximately 625 compared to conventional solid-state NMR.

96 Correlated solid-state NMR, X-ray, and electron microscopy analyses

97 osts" and applied 2D (13)C-(13)C correlation solid-state NMR to reveal the carbon-based architecture

98 er cores has been probed by (31)P and (65)Cu solid-state NMR analysis, which readily indicates that t

99 Here we describe solid state NMR measurements on the dimerization interfa

100 This paper describes solid-state NMR (SSNMR) studies of FP structure in a mem

101 Detailed solid-state NMR analysis of molecular and silica-support

102 geable side chain protons in proton-detected solid-state NMR, which is important to study protein ter

103 sing variable-temperature X-ray diffraction, solid-state NMR spectroscopy, and periodic DFT calculati

104 ntified by single crystal X-ray diffraction, solid-state NMR, and attenuated total reflectance infrar

105 Surprisingly, two-dimensional solid state NMR shows that the contact between Phe(19) a

106 structural restraints from four-dimensional solid-state NMR spectra on extensively deuterated and (1

107 nts of signals in two- and three-dimensional solid-state NMR spectra, conformation-dependent (15)N an

108 A combination of one-and two-dimensional solid-state NMR experiments was used to obtain molecular

109 as an exogenous polarization source for DNP solid-state NMR experiments.

110 urces for dynamic nuclear polarization (DNP) solid-state NMR at 9.4 T and with ca. 100 K sample tempe

111 Dynamic nuclear polarization (DNP) solid-state NMR was used to obtain natural abundance (13

112 aracterized by elemental analysis and DRIFT, solid-state NMR, and EXAFS spectroscopy.

113 elopment of BM2 inhibitors, we have employed solid-state NMR spectroscopy to investigate the conforma

114 Dynamic nuclear polarization (DNP) enhanced solid-state NMR spectroscopy at 9.4 T is demonstrated fo

115 Dynamic nuclear polarization (DNP)-enhanced solid-state NMR spectroscopy has been shown to hold grea

116 dynamic nuclear polarization (DNP)-enhanced solid-state NMR, we were able to analyze the retinal pol

117 pens new avenues for the use of DNP-enhanced solid-state NMR as an on-cell investigation tool.

118 also demonstrates the power of DNP-enhanced solid-state NMR at low temperatures for the study for se

119 They further show that DNP-enhanced solid-state NMR fills the gap for challenging membrane p

120 offers an attractive option for DNP-enhanced solid-state NMR on ordered membranes and provides a gene

121 pyridine, and (29)Si and (27)Al DNP-enhanced solid-state NMR spectroscopy.

122 ilitated tremendously by use of DNP-enhanced solid-state NMR spectroscopy.

123 also demonstrates the power of DNP-enhanced solid-state NMR to bridge the gap between functional and

124 s was generated and analyzed by DNP-enhanced solid-state NMR.

125 ld and dynamic nuclear polarization-enhanced solid-state NMR utilizing a (13)C-labeled retinal cofact

126 nuclear polarization (DNP) surface-enhanced solid-state NMR techniques.

127 nformer approaches in implicit environments, solid-state NMR restrained ensemble simulations in expli

128 model membrane protein and its experimental solid-state NMR data, we performed restrained ensemble d

129 in explicit membranes that uses experimental solid-state NMR observables to obtain the refined struct

130 the first time, to our knowledge, for (19)F solid-state NMR distance and oligomerization measurement

131 High-field solid-state NMR spectroscopy was used to visualize struc

132 ynthesized and investigated using high-field solid-state NMR spectroscopy, X-ray diffraction, atomic

133 iameter of > ca. 40 nm) can be exploited for solid-state NMR studies on membrane proteins.

134 than the proteoliposomes most often used for solid-state NMR (SSNMR) studies, and differences may aff

135 In a next step a set of four solid-state NMR angular restraints was obtained from hun

136 20/DMD simulation agree well with those from solid state NMR experiments.

137 From solid-state NMR experiments we conclude that the NOE is

138 Here, we report evidence from solid-state NMR spectroscopy that supports the presence

139 y, the FLP radical was characterized by (1)H solid state NMR spectroscopy.

140 (1)H solid-state NMR allowed the quantification of the hydrog

141 Using spin-lattice relaxation (1)H solid-state NMR at 29.49 and 13.87 MHz in the temperatur

142 idimensional single- and double-quantum (1)H solid-state NMR spectroscopy with density functional the

143 Specifically, (31)P and (2)H solid-state NMR and dual polarization interferometry (DP

144 l(-1) These results were confirmed with (2)H solid-state NMR line-shape analysis and spin-lattice rel

145 Furthermore, (31)P and (2)H solid-state NMR spectra show that liquid crystalline 1,2

146 re investigated by variable-temperature (2)H solid-state NMR spectroscopy to reveal the reorientation

147 We now use (2)H solid-state NMR to critically examine the presence and a

148 Here, solid-state NMR and EPR spectroscopy in lipid bilayer pr

149 Variations in solid state NMR signals from certain amino acid side cha

150 ce assignments remains a major bottleneck in solid-state NMR studies of protein structure and dynamic

151 ncy of dynamic nuclear polarization (DNP) in solid-state NMR studies.

152 which has been used to enhance the signal in solid-state NMR, has also been applied to the study of f

153 vel using a combination of (31)P and (139)La solid state NMR spectroscopy (SSNMR), extended X-ray abs

154 Magic-angle-spinning (MAS) solid-state NMR (ssNMR) spectroscopy allows for the dete

155 olarization (DNP) magic-angle spinning (MAS) solid-state NMR (ssNMR) spectroscopy has the potential t

156 Although magic angle spinning (MAS) solid-state NMR is a powerful technique to obtain atomic

157 Multidimensional magic angle spinning (MAS) solid-state NMR of uniformly (13)C,(15)N-labeled protein

158 beling scheme for magic angle spinning (MAS) solid-state NMR that is based on deuteration in combinat

159 tructure is validated by previously measured solid-state NMR, electron microscopy, and X-ray diffract

160 high-molecular-weight proteins, using modern solid state NMR methods.

161 nts, polymer characterization by (11)B MQMAS solid-state NMR, spectroscopic experiments with model su

162 We find that multidimensional solid state NMR spectra of (15)N,(13)C-labeled CA assemb

163 igh-resolution multinuclear/multidimensional solid-state NMR techniques, with in situ synchrotron-bas

164 We use a combination of multinuclear solid-state NMR spectroscopy, powder X-ray diffraction,

165 R is activated, we performed (13)C and (15)N solid-state NMR experiments on isotopically labeled PLP

166 Oriented (15)N solid-state NMR indicates that in membranes composed of

167 of one- and two-dimensional (13)C and (15)N solid-state NMR spectra of the formulations while preser

168 by a combined approach using (2)H and (15)N solid-state NMR spectroscopy.

169 Using (15)N solid-state NMR, we have studied protonation and H-bonde

170 ate to AuNPs is obtained by (13)C and (23)Na solid-state NMR in combination with computational modell

171 (93)Nb solid-state NMR spectra of 1a-3a and (31)P solid-state N

172 Here we report new solid-state NMR constraints that indicate antiparallel i

173 new DNP-based measurements that extend (17)O solid-state NMR beyond its current capabilities.

174 Labeling studies and (17)O solid-state NMR data confirm that two-thirds of the oxyg

175 Here, the authors use (17)O solid-state NMR spectroscopy to discriminate between oxy

176 We used (17)O solid-state NMR spectroscopy to follow this process and

177 from orientation-dependent NMR observables: solid-state NMR chemical shift anisotropy and dipolar co

178 al model for proteins with recently obtained solid-state NMR spectroscopy data and amino acid contact

179 The application of solid-state NMR spectroscopy has long been seen as an im

180 ic cycle, we report the first application of solid-state NMR spectroscopy to ThDP enzymes, whose larg

181 onstrates the principles and applications of solid-state NMR by unifying dipolar and quadrupolar inte

182 le reviews common and recent applications of solid-state NMR spectroscopy methods that provide insigh

183 A combination of solid-state NMR and circular dichroism experiments found

184 e studied in detail through a combination of solid-state NMR experiments, using labeled ethylene, and

185 Using a combination of solid-state NMR spectroscopy (ssNMR) and long molecular

186 Here we use a combination of solid-state NMR spectroscopy and potential energy landsc

187 Concepts of solid-state NMR spectroscopy and applications to fluid m

188 cording, in a matter of minutes to hours, of solid-state NMR spectra suitable for quantitative analys

189 s, as they are under the strong influence of solid-state NMR restraints.

190 In particular, the signature pattern of solid-state NMR (13)C Gln resonances that appears to be

191 ransporter protein and presents the power of solid-state NMR in this growing field.

192 ique to improve the signal to noise ratio of solid-state NMR experiments.

193 larization (DNP) enhances the sensitivity of solid-state NMR (SSNMR) spectroscopy by orders of magnit

194 rged as a tool to enhance the sensitivity of solid-state NMR experiments.

195 This was made possible by the use of solid-state NMR enhanced by dynamic nuclear polarization

196 Most structure calculations based on solid-state NMR observables are performed using simulate

197 Specifically, we employed oriented solid-state NMR data, such as dipolar couplings and chem

198 Our solid-state NMR data showed that these fibrils consist o

199 Our solid-state NMR results reveal that the N-terminal trans

200 ace complexes was further suggested by (31)P solid state NMR data which indicated the glyphosate bind

201 )Si NMR spectroscopy of the ligand and (31)P solid-state NMR of the catalyst precursor.

202 b solid-state NMR spectra of 1a-3a and (31)P solid-state NMR on their PMe3 derivatives 1b-3b led to t

203 mical bonding of phosphorus atoms with (31)P solid-state NMR spectroscopy confirmed the three-coordin

204 ntial of NMR spectroscopy, and in particular solid-state NMR, in characterising micelle-templated mes

205 By performing solid-state NMR measurements at very fast (100 kHz) magi

206 Here, we provide solid-state NMR evidence that the latter is also true of

207 s experimentally studied by (2)H and (195)Pt solid-state NMR spectroscopy (powder pattern changes wit

208 ical conditions by Rotationally Aligned (RA) solid-state NMR has two long helices, which extend well

209 rapidly acquiring high signal-to-noise ratio solid-state NMR spectra of (17)O nuclear spins and to pr

210 PGLa are in excellent agreement with recent solid state NMR experiments.

211 ese findings with the implications of recent solid-state NMR data on mature fibrils, we propose a pos

212 its relation to the fibril core, we recorded solid-state NMR and EPR data on fibrils formed by the fi

213 In this study, we report solid-state NMR site-specific measurements of the dipola

214 Here we use high-resolution solid-state NMR spectroscopy to determine the side-chain

215 om Caulobacter crescentus by high-resolution solid-state NMR spectroscopy.

216 ination motifs are measured using J-resolved solid-state NMR experiments.

217 d by (31)P/(11)B single and double resonance solid state NMR experiments.

218 chemical shifts measured by oriented sample solid-state NMR and all-atom molecular dynamics (MD) sim

219 While oriented sample solid-state NMR has provided a high-resolution backbone

220 oth magic-angle spinning and oriented-sample solid-state NMR.

221 s extent, two-dimensional homonuclear (29)Si solid-state NMR could be employed.

222 nd atomistic molecular dynamics simulations, solid-state NMR, and single channel measurements.

223 DOR process through a combination of in situ solid-state NMR spectroscopy and powder X-ray diffractio

224 The use of in situ solid-state NMR to probe the transition from intracrysta

225 a combination of reactivity studies, in situ solid-state NMR, and an extensive series of DFT calculat

226 out by X-ray diffraction, mass spectrometry, solid-state NMR, and diffuse reflectance UV-vis (DR UV-v

227 amined by DFT calculations, IR spectroscopy, solid-state NMR spectroscopy, and analysis of the Cambri

228 measurement, photoluminescence spectroscopy, solid-state NMR, and X-ray absorption spectroscopy, etc.

229 and neutron diffraction, Raman spectroscopy, solid-state NMR, transmission electron microscopy and fi

230 estraints obtained from magic-angle spinning solid-state NMR experimental data.

231 elical cross peaks from magic angle spinning solid-state NMR of a liposomal preparation strongly supp

232 eparin analogue enabled magic-angle spinning solid-state NMR of the GAG bound to 3Q fibrils, and meas

233 describe (1)H-detected magic angle spinning solid-state NMR studies of monomeric IL-8 (1-66) bound t

234 Here we present a magic angle spinning solid-state NMR study demonstrating that the NSAID sulin

235 By using magic angle spinning solid-state NMR to investigate stable isotope-labeled Im

236 r polarization enhanced magic angle spinning solid-state NMR to study this challenging membrane prote

237 Using advanced magic angle spinning solid-state NMR, we directly probe the structure of the

238 ions with the capsid by magic-angle spinning solid-state NMR.

239 We report magic-angle-spinning solid-state NMR results of the membrane-bound conformati

240 Using magic-angle-spinning solid-state NMR spectroscopy, we show that the TMD of th

241 ayers and its membrane topology using static solid-state NMR spectroscopy.

242 Surprisingly, solid-state NMR reveals that these amorphous deposits ha

243 ting a multitude of experimental techniques (solid-state NMR, AFM, SLS, DLS, FT-IR, CD) with large- a

244 stances using dipolar recoupling techniques, solid state NMR chemical shifts, and long-range side cha

245 membrane protein green proteorhodopsin that solid-state NMR could identify specific interactions at

246 helix 9 segments from the cryoEM study, the solid state NMR data lead to a unique high-resolution st

247 red segments, which do not contribute to the solid state NMR spectra.

248 The solid-state NMR approach developed here is generally app

249 The solid-state NMR chemical shifts of the PLP pyridine ring

250 ion of Bronsted acid sites: By enhancing the solid-state NMR signals of (17) O at natural abundance w

251 Here, we present the solid-state NMR atomic structure of the building block o

252 Thereby, the solid-state NMR data were used to further refine the dom

253 lyses, are shown to be inconsistent with the solid-state NMR results.

254 Though solid-state NMR spectroscopy has the potential to reveal

255 e homogeneous fibril population according to solid-state NMR analysis.

256 atural-abundance (13)C polarization transfer solid-state NMR and x-ray diffraction under similar hydr

257 um corneum (SC), using polarization transfer solid-state NMR on natural abundance (13)C in intact SC.

258 n this work, we employ polarization transfer solid-state NMR techniques to study the hydration of pri

259 MAX1 fibril network is kinetically trapped, solid-state NMR data show that fibrils within this netwo

260 Here the authors use solid-state NMR to study prion protein (PrP) amyloids fr

261 We now use solid-state NMR spectroscopy to investigate the conforma

262 We now use solid-state NMR spectroscopy to investigate the effects

263 To address this question, we use solid-state NMR and FTIR spectroscopy to define the orie

264 Here, we use solid-state NMR and neutron diffraction to investigate t

265 We use solid-state NMR spectroscopy of isotopically enriched, r

266 Here we use solid-state NMR spectroscopy to derive for the first tim

267 Here, we use solid-state NMR spectroscopy to investigate the structur

268 Here, we use solid-state NMR spectroscopy to investigate the structur

269 Here we use solid-state NMR spectroscopy to investigate the water in

270 We use solid-state NMR to determine the molecular and supramole

271 Here we use solid-state NMR, X-ray diffraction methods and mus-long

272 Here we used solid state NMR to specifically characterize the bound l

273 In the present study we have used solid-state NMR and restrained MD simulations to refine

274 ton conduction property of BM2, we have used solid-state NMR to characterize the pH-dependent structu

275 To tackle this question, we used solid-state NMR strategies providing assignments of non-

276 By using solid state NMR spectroscopy, X-ray diffraction, and ele

277 ily as ammonium carbamates, we observe using solid state NMR that the major chemisorption product for

278 Using solid-state NMR dipolar recoupling and chemical shift da

279 Using solid-state NMR spectroscopy, combined with sensitivity-

280 Using solid-state NMR, we showed that 10 of the residues exami

281 he M2 protein in phospholipid bilayers using solid-state NMR spectroscopy.

282 By using solid-state NMR structural studies, in combination with

283 an and wall teichoic acid compositions using solid-state NMR.

284 f the Rh...H-C motif can be determined using solid-state NMR spectroscopy.

285 l packing alters microsecond dynamics, using solid-state NMR measurements and multi-microsecond MD si

286 function study on the SMR protein EmrE using solid-state NMR spectroscopy in lipid bilayers and resis

287 n of their protein-ligand interactions using solid-state NMR.

288 rst study on membrane-associated pHLIP using solid-state NMR spectroscopy.

289 S), bound to mesoporous silica (SBA15) using solid-state NMR and FTIR spectroscopy.

290 complex on an amorphous silica surface using solid-state NMR measurements, enabled through a dynamic

291 membrane proteins in lipid environments via solid-state NMR.

292 ic studies of the membrane-bound protein via solid-state NMR and optical spectroscopy.

293 Whereas solid-state NMR (SSNMR) spectroscopy has recently been u

294 While solid-state NMR spectroscopic techniques have helped cla

295 A combination of multinuclear ultra-wideline solid-state NMR, powder X-ray diffraction (pXRD), X-ray

296 scale force measurements in combination with solid-state NMR spectroscopy to show that the cohesive p

297 A good correlation with solid-state NMR data indicates that the hydrophobic mome

298 prerequisite for distance measurements with solid-state NMR.

299 In this work, solid-state NMR spectroscopy is used to address these ce

300 The combined XAS, solid state NMR, and DFT data argue that the bulky catal