ライフサイエンスコーパス: hydrogen-deuterium exchange

1 s FVIII regions 2091-2104 and 2157-2162 from hydrogen-deuterium exchange.

2 ze exclusion chromatography and differential hydrogen/deuterium exchange.

3 f a VDRM compared with agonists by employing hydrogen/deuterium exchange.

4 the Collagen Toolkit peptide library and by hydrogen/deuterium exchange.

5 (e.g., HPLC, (13)C NMR, FTIR, CHN analysis, hydrogen-deuterium exchange) allowed for the analysis of

6 Hydrogen-deuterium exchange analyses of unassembled Gag

7 In this study, the application of hydrogen-deuterium exchange analysis monitored by MS pro

8 Moreover, hydrogen-deuterium exchange analysis of the point-mutate

9 ral data, molecular dynamics simulation, and hydrogen-deuterium-exchange analysis, we demonstrate tha

10 Differential hydrogen/deuterium exchange analysis demonstrates that S

11 Former studies relying on hydrogen/deuterium exchange analysis suggest that DnaC b

12 imatinib, for full-length human c-Src using hydrogen-deuterium exchange and mass spectrometry.

13 acids that make up the folding core include hydrogen-deuterium exchange and Phi-value analysis and c

14 Here, using literature data from both hydrogen-deuterium exchange and site-directed mutations,

15 X-ray fibre diffraction, hydrogen-deuterium exchange and solid-state NMR studies

16 l role of noncatalytic regions, we performed hydrogen-deuterium exchange and steady-state kinetic exp

17 By use of hydrogen/deuterium exchange and biochemical analysis, we

18 Hydrogen/deuterium exchange and chemical cross-linking c

19 Hydrogen/deuterium exchange and chemical crosslinking sh

20 Using hydrogen/deuterium exchange and cross-linking-mass spect

21 folding of DapA at peptide resolution using hydrogen/deuterium exchange and mass spectrometry.

22 receptor chimeras, photo-affinity labeling, hydrogen-deuterium exchange, and crystallography of the

23 dy, we combine small angle x-ray scattering, hydrogen-deuterium exchange, and surface plasmon resonan

24 Relaxation-dispersion NMR, hydrogen/deuterium exchange, and crystallographic data s

25 n validated by small angle x-ray scattering, hydrogen/deuterium exchange, and mass spectrometry.

26 s procedure utilized chemical cross-linking, hydrogen/deuterium exchange, and molecular modeling.

27 pull-down assays, fluorescence polarization, hydrogen/deuterium exchange, and site-directed mutagenes

28 , time-resolved electron cryo-microscopy and hydrogen/deuterium exchange as well as biochemistry, it

29 The use of hydrogen-deuterium exchange at low pH provides a measure

30 havior previously reported for catalysis and hydrogen/deuterium exchange, attributed to time scales f

31 ding in living red blood cells (RBCs), using hydrogen/deuterium exchange-based mass spectrometry (H/D

32 r the two DMS-separated ions, (5) the unique hydrogen-deuterium exchange behavior for these ions, and

33 We found differences in hydrogen-deuterium exchange between peptide-loaded and p

34 Here hydrogen-deuterium exchange by mass spectrometry and sma

35 We report that hydrogen/deuterium exchange causes a redshift in the vis

36 ormation and interactions and are namely: 1) hydrogen deuterium exchange combined with mass spectrome

37 Hydrogen-deuterium exchange combined with mass spectrome

38 Hydrogen/deuterium exchange combined with mass spectrome

39 We employed hydrogen/deuterium exchange combined with mass spectrome

40 es revealed allotype-specific differences in hydrogen-deuterium exchange, consistent with the notion

41 termination of their epitope diversity using hydrogen deuterium exchange coupled with mass spectromet

42 A combination of chemical cross-linking and hydrogen-deuterium exchange coupled to high resolution m

43 Using hydrogen-deuterium exchange coupled to mass spectrometry

44 We used hydrogen-deuterium exchange coupled to mass spectrometry

45 Using amine crosslinking and hydrogen-deuterium exchange coupled to mass spectrometry

46 time-resolved fluorescence spectroscopy, and hydrogen-deuterium exchange coupled to mass spectrometry

47 Here we show by hydrogen-deuterium exchange coupled to mass spectrometry

48 try, and mapped intermolecular contacts with hydrogen-deuterium exchange coupled to mass spectrometry

49 We used hydrogen-deuterium exchange coupled to mass spectrometry

50 We use hydrogen-deuterium exchange coupled to mass spectrometry

51 Here, we use hydrogen-deuterium exchange coupled to mass spectrometry

52 y additionally demonstrates the potential of hydrogen-deuterium exchange coupled to mass spectrometry

53 Here, using hydrogen-deuterium exchange coupled to mass spectrometry

54 avirenz on CYP46A1 by using a combination of hydrogen-deuterium exchange coupled to MS, computational

55 between apoE3 and E4 functionality, we used hydrogen-deuterium exchange coupled with a fragment sepa

56 For the current project, amide proton hydrogen-deuterium exchange coupled with MALDI-TOF mass

57 Hydrogen-deuterium exchange coupled with mass spectromet

58 horless prion protein, PrP(C), together with hydrogen-deuterium exchange coupled with mass spectromet

59 Data from controlled proteolysis and hydrogen-deuterium exchange coupled with mass spectromet

60 Hydrogen-deuterium exchange coupled with mass spectromet

61 Furthermore, hydrogen-deuterium exchange coupled with mass spectromet

62 olipid bilayer nanodiscs, subjecting them to hydrogen-deuterium exchange coupled with mass spectromet

63 Here, using hydrogen-deuterium exchange coupled with MS (HDX-MS), we

64 The approach incorporates pulsed hydrogen-deuterium exchange coupled with MS analysis.

65 nvestigated using site-directed mutagenesis, hydrogen/deuterium exchange coupled to mass spectrometry

66 Hydrogen/deuterium exchange coupled to mass spectrometry

67 Using hydrogen/deuterium exchange coupled to mass spectrometry

68 Using a combination of hydrogen/deuterium exchange coupled to NMR spectroscopy,

69 Using hydrogen/deuterium exchange coupled with mass spectromet

70 Here, we employed hydrogen/deuterium exchange coupled with mass spectromet

71 Hydrogen/deuterium exchange coupled with mass spectromet

72 tion before and after substrate binding, the hydrogen/deuterium exchange data in the L2' and 130's re

73 Here, we report amide hydrogen/deuterium exchange data that reveal long-range

74 he most promising experimental techniques is hydrogen-deuterium exchange detected by mass spectrometr

75 Hydrogen-deuterium exchange, disulfide crosslinking and

76 Unlike those approaches, pulsed hydrogen-deuterium exchange does not require modified Ab

77 ly folding residues based on pulsed labeling hydrogen deuterium exchange experiments.

78 ine temperature ramp), for the collection of hydrogen-deuterium exchange experiments as a function of

79 Notably, both hydrogen/deuterium exchange experiments and in vitro bin

80 However, hydrogen/deuterium exchange experiments confirm the seco

81 Backbone amide hydrogen/deuterium exchange experiments revealed that, i

82 Here, using hydrogen/deuterium exchange, fluorescence anisotropy, an

83 e method is based on early folding data from hydrogen deuterium exchange (HDX) data from NMR pulsed l

84 Here, we employ a combination of gas-phase hydrogen-deuterium exchange (HDX) and electron capture d

85 Hydrogen-deuterium exchange (HDX) coupled with mass spec

86 be a platform utilizing two methods based on hydrogen-deuterium exchange (HDX) coupled with mass spec

87 NMR hydrogen-deuterium exchange (HDX) experiments indicate t

88 ns of solvent-accessible surface area and by hydrogen-deuterium exchange (HDX) experiments.

89 The rate of hydrogen-deuterium exchange (HDX) in aqueous droplets of

90 In the present study, hydrogen-deuterium exchange (HDX) in conjunction with ma

91 At the same time, hydrogen-deuterium exchange (HDX) is a well-known techni

92 Here, we demonstrate the utility of hydrogen-deuterium exchange (HDX) mass spectrometry (MS)

93 e PAPf39 fibrillar core was identified using hydrogen-deuterium exchange (HDX) mass spectrometry and

94 tivity against soluble ester substrates, and hydrogen-deuterium exchange (HDX) mass spectrometry reve

95 s work, we have developed a method that uses hydrogen-deuterium exchange (HDX) of C2-hydrogens of his

96 Hydrogen-deuterium exchange (HDX) shows that AFF4 helix

97 cribe the use of a combined method including hydrogen-deuterium exchange (HDX), fast photochemical ox

98 d the E2 CD81bs by electron microscopy (EM), hydrogen-deuterium exchange (HDX), molecular dynamics (M

99 ques and methodologies such as ion mobility, hydrogen-deuterium exchange (HDX), protein footprinting

100 on cardiac troponin dynamics were mapped by hydrogen-deuterium exchange (HDX)-MS.

101 oteins under increasing pressure detected by hydrogen-deuterium exchange (HDX).

102 t the wealth of information contained in the hydrogen/deuterium exchange (HDX) behavior of peptides a

103 -principle experiments, the use of gas-phase hydrogen/deuterium exchange (HDX) combined with IMS-MS/M

104 Hydrogen/deuterium exchange (HDX) coupled to mass spectr

105 Hydrogen/deuterium exchange (HDX) coupled to mass spectr

106 Here, we applied hydrogen/deuterium exchange (HDX) coupled to mass spectr

107 nly accessible database of carefully curated hydrogen/deuterium exchange (HDX) data extracted from th

108 Protein hydrogen/deuterium exchange (HDX) followed by protease d

109 Gas-phase hydrogen/deuterium exchange (HDX) is a fast and sensitiv

110 n solution by measuring their backbone amide hydrogen/deuterium exchange (HDX) kinetics.

111 Hydrogen/deuterium exchange (HDX) mass spectrometry (MS)

112 Hydrogen/deuterium exchange (HDX) mass spectrometry (MS)

113 Hydrogen/deuterium exchange (HDX) mass spectrometry (MS)

114 Here we have used hydrogen/deuterium exchange (HDX) mass spectrometry to d

115 Here the authors employ hydrogen/deuterium exchange (HDX) mass spectrometry to s

116 NMR) spectroscopy, x-ray crystallography and hydrogen/deuterium exchange (HDX) mass spectrometry, her

117 Hydrogen/deuterium exchange (HDX) methods are widely use

118 Mass spectrometry (MS) coupled with hydrogen/deuterium exchange (HDX) offers a unique advant

119 Hydrogen/deuterium exchange (HDX) studies and MD simulat

120 icular emphasis is placed on protein NMR and hydrogen/deuterium exchange (HDX) techniques and how the

121 tonated carbohydrate structures by gas-phase hydrogen/deuterium exchange (HDX) to discover that the e

122 Top-down hydrogen/deuterium exchange (HDX) with mass spectrometri

123 Amide hydrogen/deuterium exchange (HDX), monitored by mass spe

124 structure of intact antibodies, by combining hydrogen/deuterium exchange (HDX), subzero temperature c

125 In this work, we describe a hydrogen/deuterium exchange (HDX)-based method that prov

126 ), collision-induced dissociation (CID), and hydrogen/deuterium exchange (HDX)-MS.

127 o performed mass spectrometry-detected amide hydrogen/deuterium exchange (HDXMS) experiments on Ikapp

128 ) discoidal HDL particles were determined by hydrogen-deuterium exchange (HX) and mass spectrometry m

129 Recent studies from our laboratory utilizing hydrogen-deuterium exchange in combination with mass spe

130 During this analysis, we found slow hydrogen-deuterium exchange in residues other than histi

131 e hydrolysis caused significant increases in hydrogen-deuterium exchange in sub-regions of the peptid

132 assembly steps, we analyzed the patterns of hydrogen-deuterium exchange in vimentin and in four vari

133 A simple method for hydrogen/deuterium exchange in a standard electrospray (

134 Investigation of local hydrogen/deuterium exchange in heteromultimeric protein

135 d by substantially higher protection against hydrogen/deuterium exchange in the C-terminal region nea

136 Furthermore, by comparing the hydrogen/deuterium exchange in the mature part of NGF an

137 ctions, we used mass spectrometry to monitor hydrogen/deuterium exchange in various regions of FLASH,

138 Hydrogen-deuterium exchange indicates protection of a su

139 Amide hydrogen/deuterium exchange is a commonly used technique

140 imic (compound 1) is described through amide hydrogen-deuterium exchange kinetics.

141 ns and large strain-dependent differences in hydrogen/deuterium exchange kinetics for histidine side

142 conformational dynamics of the enzyme using hydrogen/deuterium exchange kinetics.

143 Here, we use comprehensive mutagenesis and hydrogen deuterium exchange mass spectrometry (HDX-MS) t

144 Analytical ultracentrifugation and hydrogen deuterium exchange mass spectrometry suggested

145 tron microscopy (cryo-EM) and enhanced amide hydrogen-deuterium exchange mass spectrometry (DXMS) to

146 e specific intent of using the particles for hydrogen-deuterium exchange mass spectrometry (HDX MS) e

147 cific chemical modifications within the CDR, hydrogen-deuterium exchange mass spectrometry (HDX MS) w

148 Together with hydrogen-deuterium exchange mass spectrometry (HDX-MS) a

149 Using hydrogen-deuterium exchange mass spectrometry (HDX-MS) a

150 ns between beta2AR and beta-arrestin 1 using hydrogen-deuterium exchange mass spectrometry (HDX-MS) a

151 Finally, hydrogen-deuterium exchange mass spectrometry (HDX-MS) i

152 tructural integrity of therapeutic proteins, hydrogen-deuterium exchange mass spectrometry (HDX-MS) i

153 We used hydrogen-deuterium exchange mass spectrometry (HDX-MS) t

154 Here, we employ hydrogen-deuterium exchange mass spectrometry (HDX-MS) t

155 ticle (SMALP) technology can be coupled with hydrogen-deuterium exchange mass spectrometry (HDX-MS) t

156 plasmon resonance, analytical rheology, and hydrogen-deuterium exchange mass spectrometry (HXMS), we

157 ensive integrated approach of cross-linking, hydrogen-deuterium exchange mass spectrometry (MS), elec

158 revious limited tryptic digestion result and hydrogen-deuterium exchange mass spectrometry analyses p

159 ck (residues 775-818) using a combination of hydrogen-deuterium exchange mass spectrometry and isothe

160 proprotein convertase 1/3 using a histidine hydrogen-deuterium exchange mass spectrometry approach.

161 Hydrogen-deuterium exchange mass spectrometry corroborat

162 ength monomeric structure of the protein, on hydrogen-deuterium exchange mass spectrometry data, and

163 Hydrogen-deuterium exchange mass spectrometry demonstrat

164 n entropy observed in the course of the ECT, hydrogen-deuterium exchange mass spectrometry demonstrat

165 We then use hydrogen-deuterium exchange mass spectrometry experiment

166 Integration of the hydrogen-deuterium exchange mass spectrometry results wi

167 tructures of the muPA:nanobody complexes and hydrogen-deuterium exchange mass spectrometry revealed m

168 Hydrogen-deuterium exchange mass spectrometry reveals th

169 Finally, hydrogen-deuterium exchange mass spectrometry reveals th

170 NMR and amide hydrogen-deuterium exchange mass spectrometry showed tha

171 Hydrogen-deuterium exchange mass spectrometry shows that

172 In our hydrogen-deuterium exchange mass spectrometry study, 264

173 titive enzyme-linked immunosorbent assay and hydrogen-deuterium exchange mass spectrometry that 7 of

174 d fluorescence polarization measurements and hydrogen-deuterium exchange mass spectrometry to define

175 Here, we employed hydrogen-deuterium exchange mass spectrometry to describ

176 Here, we use hydrogen-deuterium exchange mass spectrometry to monitor

177 identification, native mass spectrometry and hydrogen-deuterium exchange mass spectrometry to show th

178 In this report, hydrogen-deuterium exchange mass spectrometry was used t

179 ystallography, small-angle X-ray scattering, hydrogen-deuterium exchange mass spectrometry, and mutat

180 nger in association with RPL11, we conducted hydrogen-deuterium exchange mass spectrometry, computati

181 ys11-linked diubiquitin, in combination with hydrogen-deuterium exchange mass spectrometry, enable us

182 We have applied hydrogen-deuterium exchange mass spectrometry, in conjun

183 Hydrogen-deuterium exchange mass spectrometry, limited p

184 peptides, examined through crystallographic, hydrogen-deuterium exchange mass spectrometry, mutagenes

185 ther with molecular dynamics simulations and hydrogen-deuterium exchange mass spectrometry, reveals h

186 using differential scanning fluorimetry and hydrogen-deuterium exchange mass spectrometry, we show h

187 hosphodiesterase8 (PDE8), monitored by amide hydrogen-deuterium exchange mass spectrometry, we show p

188 Using NMR and hydrogen-deuterium exchange mass spectrometry, we showed

189 sion chromatography, circular dichroism, and hydrogen-deuterium exchange mass spectrometry.

190 protomers is evident in the N197Q mutant by hydrogen-deuterium exchange mass spectrometry.

191 sed by circular dichroism, fluorescence, and hydrogen-deuterium exchange mass spectrometry.

192 ray ionization native mass spectrometry, and hydrogen-deuterium exchange mass spectrometry.

193 sing a combination of biochemical assays and hydrogen-deuterium exchange mass spectrometry.

194 ans of time-resolved electrospray ionization hydrogen-deuterium exchange mass spectrometry.

195 which this antibody binds, we have employed hydrogen-deuterium exchange mass spectrometry.

196 e mapped these regulatory interactions using hydrogen-deuterium exchange mass spectrometry.

197 donuclease active site of APE1, as mapped by hydrogen-deuterium exchange mass spectrometry.

198 Hydrogen-deuterium-exchange mass spectrometry demonstrat

199 We present the results of a hydrogen/deuterium exchange mass spectrometric (HDX-MS)

200 mbines rigid-body computational docking with hydrogen/deuterium exchange mass spectrometry (DXMS).

201 Hydrogen/deuterium exchange mass spectrometry (HDX MS) w

202 combined traditional analytical methods with hydrogen/deuterium exchange mass spectrometry (HDX MS),

203 f ion-mobility mass spectrometry (IM-MS) and hydrogen/deuterium exchange mass spectrometry (HDX-MS) a

204 Hydrogen/deuterium exchange mass spectrometry (HDX-MS) a

205 ted with protein interactions can be done by hydrogen/deuterium exchange mass spectrometry (HDX-MS) b

206 Hydrogen/deuterium exchange mass spectrometry (HDX-MS) h

207 Hydrogen/deuterium exchange mass spectrometry (HDX-MS) i

208 gher-order structure information provided by hydrogen/deuterium exchange mass spectrometry (HDX-MS) i

209 Analysis of disulfide-bonded proteins by hydrogen/deuterium exchange mass spectrometry (HDX-MS) r

210 Here, we investigate the use of hydrogen/deuterium exchange mass spectrometry (HDX-MS) t

211 Here we employ hydrogen/deuterium exchange mass spectrometry (HDX-MS) t

212 Here we use amide hydrogen/deuterium exchange mass spectrometry (HDX-MS) t

213 ody by using the complementary approaches of hydrogen/deuterium exchange mass spectrometry (HDX-MS),

214 inked IgG1 ADCs and the corresponding mAb by hydrogen/deuterium exchange mass spectrometry (HDX-MS).

215 rate mesoporphyrin (MPIX) and backbone amide hydrogen/deuterium exchange mass spectrometry (HDX-MS).

216 ha and a spectrum of oncogenic mutants using hydrogen/deuterium exchange mass spectrometry (HDX-MS).

217 proteolytic activity that is very useful for hydrogen/deuterium exchange mass spectrometry (HX-MS).

218 Library screening, other approaches, such as hydrogen/deuterium exchange mass spectrometry (MS) and X

219 terized homotypic interactions of TcpB using hydrogen/deuterium exchange mass spectrometry and hetero

220 ions targeted by 24E9 Fab were identified by hydrogen/deuterium exchange mass spectrometry and reveal

221 Using hydrogen/deuterium exchange mass spectrometry and site-d

222 Here we have applied hydrogen/deuterium exchange mass spectrometry coupled to

223 Hydrogen/deuterium exchange mass spectrometry demonstrat

224 ge is shown to increase the dynamic range of hydrogen/deuterium exchange mass spectrometry in terms o

225 Here, hydrogen/deuterium exchange mass spectrometry indicated

226 Computational docking combined with amide hydrogen/deuterium exchange mass spectrometry provided a

227 ioluminescence resonance energy transfer and hydrogen/deuterium exchange mass spectrometry reaffirms

228 Guided by hydrogen/deuterium exchange mass spectrometry results, w

229 Hydrogen/deuterium exchange mass spectrometry revealed d

230 Hydrogen/deuterium exchange mass spectrometry revealed t

231 We show by mutagenesis, pulldown and hydrogen/deuterium exchange mass spectrometry that this

232 We used the method of hydrogen/deuterium exchange mass spectrometry to address

233 Here, we use hydrogen/deuterium exchange mass spectrometry to probe t

234 Amide hydrogen/deuterium exchange mass spectrometry was used t

235 te E2-containing complexes, peptide-specific hydrogen/deuterium exchange mass spectrometry was used t

236 In this study, we used amide hydrogen/deuterium exchange mass spectrometry, a sensiti

237 isolation of neutralization escape mutants, hydrogen/deuterium exchange mass spectrometry, and X-ray

238 RIalpha complex, probed by peptide array and hydrogen/deuterium exchange mass spectrometry, brings to

239 an cAMP signaling, by a combination of amide hydrogen/deuterium exchange mass spectrometry, peptide a

240 Using hydrogen/deuterium exchange mass spectrometry, we measur

241 ed dimer were ascertained by high-resolution hydrogen/deuterium exchange mass spectrometry.

242 p and C-terminally truncated E2p proteins by hydrogen/deuterium exchange mass spectrometry.

243 face is validated by peptide mapping through hydrogen/deuterium exchange mass spectrometry.

244 d in recent years due to the introduction of hydrogen/deuterium exchange mass spectrometry.

245 nescence resonance energy transfer and amide hydrogen/deuterium exchange mass spectrometry.

246 Here, we show how hydrogen/deuterium-exchange mass spectrometry (HDX-MS) p

247 Here, we adapted hydrogen/deuterium-exchange mass spectrometry (HDX-MS) t

248 We used hydrogen/deuterium-exchange mass spectrometry and small-

249 By hydrogen/deuterium-exchange mass spectrometry, these HIC

250 Next, hydrogen-deuterium exchange-mass spectrometry (HDX-MS) w

251 Using Hydrogen-Deuterium Exchange-Mass Spectrometry (HDX-MS) w

252 mains one of the most serious limitations of hydrogen/deuterium exchange-mass spectrometry (HDX-MS),

253 By monitoring PARP-1 dynamics using hydrogen/deuterium exchange-mass spectrometry (HXMS), we

254 can analysis, site-directed mutagenesis, and hydrogen/deuterium exchange-mass spectrometry.

255 ction based on biophysical measurements with hydrogen-deuterium exchange/mass spectrometry, surface p

256 exchange rapidly with water as indicated by hydrogen-deuterium exchange measurements.

257 ined methods of solution state NMR and amide hydrogen/deuterium exchange measurements with mass spect

258 standardized a simple and economical online hydrogen-deuterium exchange methodology, which can be us

259 Using hydrogen/deuterium exchange monitored by Fourier transfo

260 Hydrogen/deuterium exchange monitored by mass spectromet

261 tural properties of TG2 in solution by using hydrogen/deuterium exchange monitored by mass spectromet

262 ion of disulfide bond-containing proteins by hydrogen/deuterium exchange monitored by mass spectromet

263 Here, equilibrium unfolding and hydrogen/deuterium exchange monitored by mass spectromet

264 -directed mutagenesis, resonance Raman (RR), hydrogen-deuterium exchange MS (HDX-MS) methods, and mol

265 Herein, we employed hydrogen-deuterium exchange MS (HDXMS) to spatially reso

266 Hydrogen-deuterium exchange MS revealed that membrane-re

267 Hydrogen-deuterium exchange MS reveals structural change

268 ipid kinase assays and through analysis with hydrogen-deuterium exchange MS.

269 In this work, hydrogen/deuterium exchange MS (H/DX-MS) was used to map

270 e binding site of a bactericidal antibody by hydrogen/deuterium exchange MS shows that a protective c

271 pendence represents an advantage compared to hydrogen/deuterium exchange MS.

272 Using hydrogen-deuterium exchange NMR and fluorescence quenchi

273 el and convenient protocol for the catalytic hydrogen-deuterium exchange of biologically active terti

274 We report the use of NMR-detected hydrogen-deuterium exchange of quenched cell lysates to

275 Molecular dynamics simulations and hydrogen/deuterium exchange of Hsp90-dependent Src kinas

276 ve MS-based analytical method to measure the hydrogen/deuterium exchange of proteins in solution, we

277 By measuring hydrogen-deuterium exchange patterns of peptide bond ami

278 thin non-covalent complexes as unravelled by hydrogen-deuterium exchange processes performed in the g

279 We determined the amide hydrogen/deuterium exchange profile of native human fibr

280 liquid chromatography and mass spectrometry, hydrogen/deuterium exchange provides several unique adva

281 ity capture of biotinylated antibodies under hydrogen/deuterium exchange quench conditions by the bio

282 oteins even under the extreme conditions for hydrogen/deuterium exchange quenching i.e. pH 2.5 and 0

283 kening helical hydrogen bonds and increasing hydrogen-deuterium exchange rate (kex).

284 ol-2-ylidene, the so-called IDipp, catalyzes hydrogen/deuterium exchange reactions between pseudoacid

285 Our hydrogen-deuterium exchange results suggest that heterog

286 e dynamics of the complex were defined using hydrogen-deuterium exchange, revealing a novel 20-residu

287 In combination with hydrogen/deuterium-exchange, solution scattering data an

288 Hydrogen-deuterium exchange studies coupled with mass sp

289 pray ionization mass spectrometry coupled to hydrogen-deuterium exchange studies followed by mutageni

290 Hydrogen/deuterium exchange studies provided a global es

291 Hydrogen/deuterium exchange studies reveal that GQ-16 st

292 Here, we used NMR measurements of hydrogen-deuterium exchange to determine the stability o

293 Here we use hydrogen/deuterium exchange to examine the interactions

294 biotin-streptavidin capture strategy allows hydrogen/deuterium exchange to occur in proteins in solu

295 sualize global structural reorganization and hydrogen/deuterium exchange to track changes in local co

296 Hydrogen-deuterium exchange was used to map the Rag bind

297 Using hydrogen/deuterium exchange, we demonstrate that ligatio

298 er protonic species undergo room-temperature hydrogen-deuterium exchange with an alkane hydrocarbon r

299 Amide hydrogen/deuterium exchange with mass spectrometric anal

300 Hydrogen/deuterium exchange with mass spectrometric anal