ライフサイエンスコーパス: ion mobility

1 o denaturation on cross-linked species using ion mobility.

2 Ion mobility analysis reveals that within each charge st

3 ell and the second IMS stage for the product ion mobility analysis.

4 ructure characterization techniques, such as ion mobility and computational modeling.

5 n both electrodes individually, including Li-ion mobility and its changes with temperature.

6 d by buffers rich in He or H(2) that elevate ion mobility and lead to prominent non-Blanc effects.

7 nce sensitivity while having high-resolution ion mobility and mass capabilities.

8 Ion mobility and mass spectrometry techniques are couple

9 Adapting ion mobility and soft-landing methodologies, we showed h

10 -ICR MS by performing chemical formula-based ion mobility and tandem MS analysis for the structural c

11 ubChem database were screened based on their ion mobility and the MS/MS matching score.

12 This cell was installed between the ion mobility and time-of-flight regions of the instrumen

13 a were examined by native mass spectrometry, ion mobility, and quantitative peptide mapping.

14 The resulting ion mobilities are directly correlated to the average li

15 Super-ionic solids, which exhibit ion mobilities as high as those in liquids or molten sal

16 re property of ETL indirectly impacts halide ion mobility as evident from the TiO(2)-assisted halide

17 (FAIMS) separate them by the change of their ion mobility at high fields.

18 s paddlewheel dynamics contribute to Lithium-ion mobility at room temperature.

19 atmospheric pressure, (ii) ambient pressure ion mobility-based instruments, and (iii) high flow rate

20 Here, the ion mobility behavior of several sets of isomeric glycan

21 Capillary zone electrophoresis and ion mobility both coupled to mass spectrometry were used

22 f molecular dynamics, quantum chemistry, and ion mobility calculations, to generate structures and ch

23 This work shows that ion mobility can be incorporated with liquid chromatogra

24 eparation region modified to accept a cyclic ion mobility (cIM) device.

25 separation is achievable by using drift tube ion mobility coupled with high-resolution mass spectrome

26 al cross sections (CCS), we created the PNNL Ion Mobility Cross Section Extractor (PIXiE).

27 The added ion mobility data dimension dramatically increased the p

28 The inclusion of ion mobility data in widely adopted confidence levels fo

29 althy controls using label-free quantitative ion-mobility data independent analysis mass spectrometry

30 rom the greater reduced mass contribution to ion mobility described by the Mason-Schamp relationship.

31 lecular weight and ion mobility in a trapped ion mobility device (timsTOF Pro) to devise a scan mode

32 data extraction workflow by inclusion of the ion mobility dimension for both signal extraction and sc

33 lexing" (HRdm), to improve resolution in the ion mobility dimension.

34 However, analysis of ion mobility distributions reveals the two-state transit

35 higher capacitance but suffer from inhibited ion mobility due to constriction of the GO interlayer sp

36 e ion mobility spectrum agree with the basic ion mobility equation when using nitrogen as drift gas a

37 alizing reproducible gas-phase measurements, ion mobility experiments are commonly conducted in the p

38 cids using low-pressure, ambient-temperature ion mobility experiments performed in a radio frequency-

39 in differential or field asymmetric waveform ion mobility (FAIMS) spectra depending on the ion geomet

40 und those envelopes to split in differential ion mobility (FAIMS) spectra in a manner dependent on th

41 drift cell that enables the determination of ion mobilities from "first principles", we directly dete

42 es, with recently special interest in native ion mobility (IM) and collision induced unfolding (CIU)

43 The use of ion mobility (IM) as an additional level of separation c

44 ding to their conformation in the gas phase, ion mobility (IM) coupled to mass spectrometry is an att

45 Ion mobility (IM) is a gas-phase separation technique th

46 Periodic focusing (PF)-drift tube (DT)-ion mobility (IM) provides first-principles determinatio

47 Ion mobility (IM) separates ions based on their response

48 icient ion population compression for use in ion mobility (IM) separations.

49 entary biophysical techniques, including MS, ion mobility (IM), CD, and FTIR spectroscopy assays.

50 Ion mobility (IM)-based collision-induced unfolding (CIU

51 ended liquid chromatographic separation, and ion mobility (IM)-MS for efficient separation and identi

52 tion-mass spectrometry (ESI-MS) and nano-ESI-ion mobility (IM)-MS with collision-induced unfolding (C

53 e of the correlation of molecular weight and ion mobility in a trapped ion mobility device (timsTOF P

54 to inhomogeneities in topography and lithium-ion mobility in both the inner- and outer-SEI, thanks to

55 et was used to evaluate the value of product ion mobility in identifying lipids in a complex mixture.

56 Halide ion mobility in metal halide perovskites remains an intr

57 reviously acquired on traveling-wave (TWIMS) ion mobility in the context of native mass spectrometry

58 electrode, is attributed to increased sodium ion mobility in the dendrite.

59 phase conformations which are resolved using ion mobility; in contrast, the inactive epimer, 3-epi-25

60 s temperature and humidity using an accurate ion mobility instrument.

61 Modern ion mobility instrumentation is typically operated above

62 ternating electric field during differential ion mobility is critical for separation selectivity and

63 The coupling of SID, high resolution, and ion mobility is demonstrated for a variety of protein co

64 redictions also indicate that high magnesium ion mobility is possible in other chalcogenide spinels,

65 here anion reorientations are negligible and ion mobility is reduced.

66 n accurate to, at best, +/-2% of the reduced ion mobility (K(0)) value of the chemical of interest.

67 intact HS saccharides are dissociated in an ion mobility mass spectrometer and collision cross secti

68 Here, we modified a traveling wave ion mobility mass spectrometer to enable IMRs in the tra

69 Five ion mobility mass spectrometers utilizing commercially a

70 N) approach to deconvolute Fourier transform ion mobility mass spectrometry (FT-IMMS) drift time spec

71 Ion mobility mass spectrometry (IM-MS) allows separation

72 More recently, ion mobility mass spectrometry (IM-MS) has emerged as an

73 Herein, native ion mobility mass spectrometry (IM-MS) is employed to me

74 iology, collision cross sections (CCSs) from ion mobility mass spectrometry (IM-MS) measurements are

75 ompounds have recently been established from ion mobility mass spectrometry (IM-MS) measurements.

76 electrospray ionization (ESI) together with ion mobility mass spectrometry (IM-MS) to study soluble

77 e field of native mass spectrometry (MS) and ion mobility mass spectrometry (IM-MS).

78 estigations of full-length UVR8 using native ion mobility mass spectrometry adapted for photoactivati

79 Single-pass cyclic ion mobility mass spectrometry enabled the detection of

80 Here, native ion mobility mass spectrometry is employed to directly m

81 rmined by liquid extraction surface analysis ion mobility mass spectrometry of native and denatured p

82 Here, we develop a "Shotgun" Ion Mobility Mass Spectrometry Sequencing (SIMMS(2)) met

83 ut of four ligands), together with DOSY NMR, ion mobility mass spectrometry, and X-ray structure resu

84 Other methods used include ion mobility mass spectrometry, gas chromatography-mass

85 Using ion mobility mass spectrometry, we show how specific O-g

86 ng mutations that mimic phosphorylation, and ion mobility mass spectrometry, we show that successive

87 their interactions with ligands using native ion mobility mass spectrometry.

88 lts from DFT calculations and traveling wave ion mobility mass spectrometry.

89 ere considered and analyzed using drift time ion mobility mass spectrometry.

90 collision cross sections were observed using ion mobility mass spectrometry.

91 COSY, NOESY, DOSY) NMR spectroscopy, ESI-MS, ion-mobility mass spectrometry (IM-MS), AFM, and TEM.

92 Crystallographic and native ion-mobility mass spectrometry data show that the TIH-bo

93 Ion-mobility mass spectrometry reveals broadly similar g

94 otein complexes and are also compatible with ion-mobility mass spectrometry, paving the way for impro

95 into the electrospray interface of a trapped ion mobility-mass spectrometer for rapid diastereomer se

96 modifications to an Agilent 6560 drift tube ion mobility-mass spectrometer in order to perform robus

97 ent with the results obtained from cryogenic ion mobility-mass spectrometry (cryo-IM-MS) measurements

98 ydrophilic interaction liquid chromatography-ion mobility-mass spectrometry (HILIC-IM-MS) has shown a

99 Ion mobility-mass spectrometry (IM-MS) affords unique ad

100 lity of commercial instrumentation have made ion mobility-mass spectrometry (IM-MS) an increasingly p

101 A multidimensional ion mobility-mass spectrometry (IM-MS) analytical platfo

102 ss section (CCS) measurements resulting from ion mobility-mass spectrometry (IM-MS) experiments provi

103 fication of features derived from untargeted ion mobility-mass spectrometry (IM-MS) experiments.

104 Ion mobility-mass spectrometry (IM-MS) has become a powe

105 Ion mobility-mass spectrometry (IM-MS) has become an imp

106 ented on a commercially available drift tube ion mobility-mass spectrometry (IM-MS) instrument and ut

107 Ion mobility-mass spectrometry (IM-MS) is a rapid, two-d

108 Native ion mobility-mass spectrometry (IM-MS) is capable of rev

109 Ion mobility-mass spectrometry (IM-MS) measurements show

110 Ion mobility-mass spectrometry (IM-MS) provides rapid tw

111 Here, using native ion mobility-mass spectrometry (IM-MS) we find that alph

112 to nanoparticles using atmospheric-pressure ion mobility-mass spectrometry (IM-MS), and we demonstra

113 Ion mobility-mass spectrometry (IM-MS), tandem mass spec

114 Using liquid chromatography-drift tube ion mobility-mass spectrometry (LC-DTIM-MS), a qualitati

115 Using native nano-electrospray ionisation ion mobility-mass spectrometry (nESI-IM-MS), we characte

116 on of microalgae extracts via traveling wave ion mobility-mass spectrometry (TWIM-MS) by two differen

117 geted ultraperformance liquid chromatography-ion mobility-mass spectrometry (UPLC-IM-MS) method was o

118 Ion mobility-mass spectrometry and collision induced unf

119 transmission electron microscopy, as well as ion mobility-mass spectrometry coupled to infrared (IR)

120 ed structures for lossless ion manipulations ion mobility-mass spectrometry platform (SLIM IM-MS), in

121 rcular dichroism, (1)H NMR, and electrospray ion mobility-mass spectrometry studies.

122 Here, we use high precision ion mobility-mass spectrometry to compile a structural d

123 ere, we use kinetics measurements and native ion mobility-mass spectrometry to show that SERF mainly

124 the measurement of protein structures, with ion mobility-mass spectrometry, which provides shape and

125 es by ultraperformance liquid chromatography ion mobility-mass spectrometry.

126 es of the cluster formation and experimental ion mobility measurements (CoV dispersion plots) conside

127 improving the sensitivity and resolution of ion mobility measurements is described.

128 ved fragmentation pattern, and complementary ion mobility measurements prior to ECD provided orthogon

129 spectrometry (MS) techniques, namely native ion mobility MS (IM-MS), collision-induced unfolding (CI

130 ere, we demonstrate that the combined use of ion-mobility MS and well-defined synthetic glycan standa

131 related point mutants by using tandem MS and ion-mobility MS as a function of collisional activation.

132 processing native mass spectrometry (MS) and ion mobility-MS data sets and provide a brief overview o

133 The effect of humidity on reduced ion mobilities of TAA cations is discussed.

134 The high resolution afforded by the ion mobility-Orbitrap mass analyzer provides new opportu

135 a native electrospray ionization drift tube ion mobility-Orbitrap mass spectrometer specifically des

136 wed that conductivity is being controlled by ion mobility over these RH.

137 tion (MALDI), including MALDI-MS imaging and ion mobility, particularly high-field asymmetric wavefor

138 IMS bands were assigned to the heterogeneous ion mobility profile of [C(18)H(18)O(10)-H](-), and cand

139 traveling wave (TW) based compression ratio ion mobility programming (CRIMP) approach within structu

140 ected superposition approximation (PSA), the Ion Mobility Projection Approximation Calculation Tool (

141 geted peptide quantification using a trapped ion mobility quadrupole time-of-flight mass spectrometer

142 ced postionization, or MALDI-2, to a trapped ion mobility quadrupole time-of-flight mass spectrometer

143 g powers but are ultimately limited in their ion mobility range because of the range of mobilities sp

144 based instrument, accurate K(0) values of an ion mobility reference standard need to be used for ion

145 In addition, an ion mobility resolution (CCS centroid divided by CCS fwh

146 for pyruvate kinase (MW ~ 233 kDa); however, ion mobility resolution for bovine serum albumin (MW ~ 6

147 ss" separations provide unprecedentedly high ion mobility resolving powers but are ultimately limited

148 ility reference standard need to be used for ion mobility scale calibration.

149 Integration of multiplexed ion mobility scans is also shown to increase extracted a

150 Although ion mobility separates the epimers, some chromatography

151 Ion mobility separation (IMS) combined with HRMS instrum

152 The utilization of ion mobility separation (IMS) improved the molecular cov

153 An alternative to this is to perform ion mobility separation before ion detection, enabling t

154 Ion mobility separation can add an orthogonal analytical

155 and-release (CaR)-ESI-MS assay, carried with ion mobility separation prior to GBP "release" (i.e., Ca

156 FPOP coupled with native ion mobility separation shows that exposure to H(2)O(2)

157 Integration of ion mobility separation to LESA mass spectrometry workfl

158 ring up to six peptides from a single 100 ms ion mobility separation with the current setup.

159 In the absence of ion mobility separation, 21 proteins were detected in ra

160 tiplexing capability provided by the trapped ion mobility separation, allowing more than 200 peptides

161 of the instrument, including mass selection, ion mobility separation, and post-mobility fragmentation

162 Altogether, combining FPOP, ion mobility separation, and top-down and bottom-up mass

163 , the instrument allows multiple pass cyclic ion mobility separation, with concomitant increase in re

164 zation approach with high-resolution trapped ion mobility separation.

165 ctivity provided by a postsampling gas-phase ion mobility separation.

166 e liquid chromatography (UPLC) coupled to an ion-mobility separation (IMS) quadrupole-time-of-flight

167 Integrating ion mobility separations aids in deconvoluting these com

168 es wider mobility range ultrahigh-resolution ion mobility separations and expands on the ability of S

169 first time that the current state-of-the-art ion mobility separations benchmark at a CCS-based resolv

170 When coupling drift-tube gas-phase ion mobility separations with ion trapping mass analyzer

171 gnificantly increased the resolving power of ion mobility separators.

172 Ion mobility spectra of citric acid (CA) are complex, an

173 on values to be directly determined from all ion mobility spectra.

174 e performance of a small, plastic drift tube ion mobility spectrometer (DT-IMS) is described.

175 This novel field asymmetric time of flight ion mobility spectrometer (FAT-IMS) allows high repetiti

176 ate CID in a field asymmetric time of flight ion mobility spectrometer (FAT-IMS).

177 rimental characterization of the flexible DT ion mobility spectrometer (Flex-DT-IMS) with correspondi

178 A tandem ion mobility spectrometer (IMS(2)) built from two differ

179 A tandem ion mobility spectrometer at ambient pressure with a rea

180 ble drift tube (DT) along with an associated ion mobility spectrometer system.

181 compounds at ambient pressure using a tandem ion mobility spectrometer with a reactive stage between

182 lemented by coupling a 3D-printed drift tube ion mobility spectrometer, operated at atmospheric press

183 Drift tube ion mobility spectrometers (DT-IMS) separate ions by the

184 w field ion mobility, while field asymmetric ion mobility spectrometers (FAIMS) separate them by the

185 Ion mobility spectrometers (IMS) with field switching io

186 Particularly in field applications, ion mobility spectrometers (IMSs) are useful because of

187 us, they are an excellent choice for compact ion mobility spectrometers with both high resolving powe

188 rrors were all within 1-2% of the drift tube ion mobility spectrometry (DTIMS) measurements, with low

189 g electrospray ionization coupled to trapped ion mobility spectrometry (ESI-TIMS).

190 lity to mass spectrometry makes differential ion mobility spectrometry (FAIMS) a powerful tool for is

191 Strong orthogonality between differential ion mobility spectrometry (FAIMS) and mass spectrometry

192 Full scan field asymmetric waveform ion mobility spectrometry (FAIMS) combined with liquid c

193 trategy using high-field asymmetric waveform ion mobility spectrometry (FAIMS) coupled to the Orbitra

194 d aerodynamic high-field asymmetric waveform ion mobility spectrometry (FAIMS) device into the phosph

195 High-field asymmetric waveform ion mobility spectrometry (FAIMS) enables the separation

196 e benefits of high field asymmetric waveform ion mobility spectrometry (FAIMS) for mass spectrometry

197 ass spectrometric analysis, field asymmetric ion mobility spectrometry (FAIMS) has previously been us

198 d to MS via a high-field asymmetric waveform ion mobility spectrometry (FAIMS) interface to evaluate

199 High field asymmetric waveform ion mobility spectrometry (FAIMS) is an orthogonal separ

200 High-field Asymmetric Waveform Ion Mobility Spectrometry (FAIMS) is used to improve qua

201 e coupling of high-field asymmetric waveform ion mobility spectrometry (FAIMS) separation into the LE

202 s, differential or field asymmetric waveform ion mobility spectrometry (FAIMS) was implemented at or

203 I-MS) coupled with field asymmetric waveform ion mobility spectrometry (FAIMS), predictive metabolic

204 itching using high-field asymmetric waveform ion mobility spectrometry (FAIMS), we identified multipl

205 particularly high-field asymmetric waveform ion mobility spectrometry (FAIMS).

206 e measured by high-field asymmetric waveform ion mobility spectrometry (FAIMS).

207 ion (SPS) and high-field asymmetric waveform ion mobility spectrometry (FAIMS).

208 ced forms, was investigated by gated-trapped ion mobility spectrometry (G-TIMS).

209 /HS isomers may be resolved by gated-trapped ion mobility spectrometry (gated-TIMS) with negligible s

210 to study the potential of gas chromatography-ion mobility spectrometry (GC-IMS) to differentiate lact

211 ue termed high asymmetric longitudinal field ion mobility spectrometry (HALF-IMS), which allows separ

212 findings allow for integration of MS(2) with ion mobility spectrometry (IM-MS(2)) and lead to a strat

213 trace chemical detection techniques such as ion mobility spectrometry (IMS) and differential mobilit

214 ation (vt-ESI) technique in combination with ion mobility spectrometry (IMS) and mass spectrometry (M

215 rature electrospray ionization combined with ion mobility spectrometry (IMS) and mass spectrometry (M

216 T) electrospray ionization (ESI) paired with ion mobility spectrometry (IMS) and mass spectrometry (M

217 Ion Mobility Spectrometry (IMS) coupled to Gas Chromatog

218 ctures for lossless ion manipulations (SLIM) ion mobility spectrometry (IMS) device capable of switch

219 ar gas chromatography (GC) column coupled to ion mobility spectrometry (IMS) has been explored to cla

220 Ion mobility spectrometry (IMS) has proven to be useful

221 MD) simulations, mass spectrometry (MS), and ion mobility spectrometry (IMS) in positive ion mode.

222 Ion mobility spectrometry (IMS) is an excellent tool for

223 Native mass spectrometry (MS) coupled with ion mobility spectrometry (IMS) is emerging as an import

224 ion cross section (CCS) values obtained from ion mobility spectrometry (IMS) measurements were recent

225 We reported the capability of ion mobility spectrometry (IMS) methods to resolve such

226 F separation fields normally associated with ion mobility spectrometry (IMS) or differential mobility

227 olome of live microglial cells by drift-tube ion mobility spectrometry (IMS) quadrupole time-of-fligh

228 ork, we demonstrate the advantages of adding ion mobility spectrometry (IMS) separation to existing L

229 mance liquid chromatography (chip-HPLC) with ion mobility spectrometry (IMS) via fully integrated ele

230 While the recent combination of ion mobility spectrometry (IMS) with cryogenic IR spectr

231 Ion mobility spectrometry (IMS) with mass spectrometry h

232 While combining ion mobility spectrometry (IMS) with tandem mass spectro

233 yed a combination of mass spectrometry (MS), ion mobility spectrometry (IMS), and molecular dynamics

234 Ion mobility spectrometry (IMS)-based instruments have h

235 ically around a few microseconds or less for ion mobility spectrometry (IMS)-based separations on the

236 lision cross section (CCS) values when using ion mobility spectrometry (IMS).

237 on of chip-electrochromatography (ChEC) with ion mobility spectrometry (IMS).

238 We demonstrate that trapped ion mobility spectrometry (TIMS) can resolve matrix peak

239 recursor ions are accumulated in the trapped ion mobility spectrometry (TIMS) cells and separated acc

240 light (Q-TOF) mass spectrometer with trapped ion mobility spectrometry (TIMS) enables a >250% increas

241 l heating experienced by ions during trapped ion mobility spectrometry (TIMS) experiments.

242 on liquid chromatography coupled to trapped ion mobility spectrometry (TIMS) for separation and tand

243 the combination of MALDI-2 with the trapped ion mobility spectrometry (TIMS) functionality of the in

244 For the first time, trapped ion mobility spectrometry (TIMS) in tandem with Fourier

245 Trapped ion mobility spectrometry (TIMS) is presented as a new a

246 CCS calibration accuracy with traveling wave ion mobility spectrometry (TWIMS) separations in structu

247 NMR and MS-hybridized technologies including ion mobility spectrometry and IR spectroscopy.

248 vitamin D from its inactive epimer; however, ion mobility spectrometry can distinguish the epimer pai

249 by liquid chromatography with traveling-wave ion mobility spectrometry coupled to high resolution mas

250 rpentine ultralong path and extended routing ion mobility spectrometry coupled to mass spectrometry (

251 Gas chromatography-ion mobility spectrometry enables noninvasive, rapid, an

252 at shows the potential of gas chromatography-ion mobility spectrometry for early detection of ventila

253 s that depend on the drift times measured by ion mobility spectrometry for repeating units released a

254 Gas chromatography-ion mobility spectrometry gas analysis, CT scans of the

255 The dual separation in gas chromatography-ion mobility spectrometry generates complex multi-dimens

256 Ion mobility spectrometry is a powerful detection method

257 neumonia we determined if gas chromatography-ion mobility spectrometry is able to detect 1) ventilato

258 Fourier transform-ion mobility spectrometry is implemented by coupling a 3

259 que combination of preseparation and trapped ion mobility spectrometry separation in the negative ion

260 ein, we report on the use of high-resolution ion mobility spectrometry separations in structures for

261 The combination of field asymmetric waveform ion mobility spectrometry with liquid chromatography-mas

262 te the use of coupled liquid chromatography, ion mobility spectrometry, and mass spectrometry (LC-IMS

263 ing wave, trapped, and high-field asymmetric ion mobility spectrometry, are evaluated for their abili

264 increase in applications of native mass and ion mobility spectrometry, especially for the study of p

265 which is why orthogonal techniques, such as ion mobility spectrometry, have been explored.

266 loid-beta oligomers by mass spectrometry and ion mobility spectrometry, revealing functionally releva

267 Ion mobility spectrometry-mass spectrometry (IMS-MS) and

268 Ion mobility spectrometry-mass spectrometry (IMS-MS) com

269 esults suggested that paper spray ionization-ion mobility spectrometry-mass spectrometry (PSI-IMS-MS)

270 ere, we assess the ability of tandem-trapped ion mobility spectrometry-mass spectrometry (tandem-TIMS

271 phy (LC) followed by high resolution trapped ion mobility spectrometry-mass spectrometry (TIMS-MS) wa

272 By using trapped ion mobility spectrometry-mass spectrometry (TIMS-MS), s

273 amyloid intermediates using a combination of ion mobility spectrometry-mass spectrometry and gas-phas

274 loride ions using a novel technique coupling ion mobility spectrometry-mass spectrometry with infrare

275 dimerization as determined by native trapped ion mobility spectrometry-mass spectrometry.

276 el analytical method based on hybrid trapped ion mobility spectrometry-time-of-flight mass spectromet

277 l information for spectral interpretation in ion mobility spectrometry.

278 is and resolution of isomers, including from ion mobility spectrometry.

279 laser desorption/ionization (MALDI) trapped ion-mobility spectrometry (TIMS) imaging platform.

280 pid screening method based on traveling-wave ion-mobility spectrometry (TWIMS) combined with tandem m

281 where mass-selected structural studies using ion-mobility spectrometry mass spectrometry (IMS-MS) cou

282 gnals were detected by multicapillary column ion-mobility spectrometry, of which 44 could be identifi

283 als and analyzed using multicapillary column ion-mobility spectrometry.

284 this effect, high-Field Asymmetric-waveform Ion Mobility Spectroscopy (FAIMS) has been proposed as a

285 The observed peak shifts in the ion mobility spectrum agree with the basic ion mobility

286 been limited by the modest resolution of the ion mobility stage.

287 Moreover, the lithium ion mobility structurally indicated by a disordered Li/S

288 ids across 117 lipid subclasses and included ion mobility tandem mass spectrometry.

289 an be obtained from measurements made of the ions mobility through a given gas, and such structural i

290 aper, laser ablation electrospray ionization ion mobility time-of-flight mass spectrometry (LAESI-IMS

291 abilities in general, and to this quadrupole-ion mobility-time-of-flight (Q-IM-TOF) mass spectrometer

292 re, we report the use of a quadrupole-cyclic ion mobility-time-of-flight mass spectrometer (Q-cIM-ToF

293 pture dissociation (ECD) within a quadrupole/ion mobility/time-of-flight mass spectrometer.

294 The ion mobility trap allows measuring up to six peptides fr

295 Ion mobility was integrated with liquid chromatography/h

296 High-field asymmetric ion mobility was unable to resolve a unique peak but det

297 Native mass spectrometry and ion mobility were used to assess collision cross section

298 been achieved, owing to their high intrinsic ion mobility, which leads to interdiffusion and large ju

299 ons by the absolute value of their low field ion mobility, while field asymmetric ion mobility spectr

300 eation of CCS databases and the inclusion of ion mobility within identification criteria are of high