ライフサイエンスコーパス: FTICR-MS

1 FTICR MS-observed methylation ladders identify an ensemb

2 FTICR MS/MS demonstrated its promising role as a structu

3 FTICR-MS analysis of a size-uniform fraction of bikunin

4 FTICR-MS formulas assigned to PARAFAC components represe

5 Finally, nano-DESI 21T FTICR MS imaging is demonstrated to reveal images corres

6 tion electrospray ionization (nano-DESI) 21T FTICR MS in ~5 h using 768 ms transients, producing over

7 Ultrahigh performance 21T-FTICR-MS enabled the simultaneous capture of isotopic fi

8 Until now 2D FTICR MS afforded only a moderate resolution for precurs

9 on cyclotron resonance mass spectrometry (2D FTICR MS or 2D MS) allows direct correlation between pre

10 Here, we report that 2D FTICR MS using nonuniform sampling (NUS) obtained by ran

11 We demonstrated the applicability of SWIM 2D-FTICR MS/MS to two diverse samples of industrial importa

12 h PARAFAC components numbered from 39 to 572 FTICR-MS derived elemental formulas.

13 1000, which may only be resolved by advanced FTICR-MS instrumentation.

14 the first implementation and results from an FTICR MS with fully integrated dual accumulation analysi

15 hniques has shown that EID carried out on an FTICR MS and CID performed on a linear ion trap MS produ

16 In this study, we describe an FTICR-MS-based method for rapid, nontargeted screening o

17 ations for TOF MS (51.1 +/- 4.4 pmol/mg) and FTICR MS (56.9 +/- 6.0 pmol/mg) did not significantly di

18 IM/MS and FTICR MS results reveal an increase in compositional com

19 ve been detected using this microreactor and FTICR-MS system.

20 GC-MS and FTICR-MS revealed no significant bitumen alteration for

21 sform ion cyclotron resonance (FTICR)-MS and FTICR-MS top-down experiments using a variety of dissoci

22 clotron resonance mass spectrometry (GC-APCI-FTICR MS) for the study of environmental samples from th

23 We also applied LD/APPCI FTICR MS for rapid analysis of sodium and calcium naphth

24 ss-to-charge unit window was accomplished by FTICR MS at 9.4 T.

25 ecent strategies for SOM characterization by FTICR MS with emphasis on SOM sample collection, prepara

26 ylation reactions, respectively, followed by FTICR MS analyses.

27 The improved resolution offered by FTICR MS allowed assignment of four polymeric series dif

28 tegy and ultrahigh mass accuracy provided by FTICR MS allow for rapid and unequivocal assignment of r

29 three successive vintages, were analysed by FTICR-MS.

30 ied using redundant HDX-MS data generated by FTICR-MS.

31 aging on lees in bottle was investigated by FTICR-MS and UPLC-Q-TOF-MS.

32 of high DBE oil components, unobservable by FTICR-MS until oxygenation in the mesocosms.

33 n (ESI)-collision-induced dissociation (CID)-FTICR MS was applied to identify protein isoforms that c

34 n cyclotron resonance mass spectrometry (CID-FTICR MS) was developed to determine structural building

35 r composition of seven DOM compound classes (FTICR-MS) and attenuation of 17 polar TrOCs in a small u

36 DAPPI FTICR MS results agree with bulk elemental composition a

37 In this work, the advantages of DI-FTICR MS and SFC-FTICR MS proved complementary, and DI w

38 on cyclotron resonance mass spectrometer (DI-FTICR MS) with an electrospray ionization source (ESI).

39 Using DI-FTICR MS, 9644 metabolic features were detected where 71

40 liquid chromatography (UHPLC) followed by DI-FTICR-MS.

41 ncrease of identifications compared to EO-DI-FTICR-MS using the same volume of starting material.

42 veform ion modulation (SWIM) two-dimensional FTICR MS/MS.

43 phase structural heterogeneity, and top-down FTICR-MS/MS provides in-depth glycoform analysis for una

44 ection of a subset of polypeptides from each FTICR MS acquisition.

45 Our study of SOM molecules by ESI FTICR MS revealed new insight into the molecular-level c

46 bound calmodulin dimers were observed by ESI FTICR MS.

47 mponents of complex mixtures by negative ESI FTICR MS.

48 n cyclotron resonance mass spectrometry (ESI FTICR-MS) permitted the identification of several major

49 ultrahigh resolution mass spectrometry (ESI FTICR-MS) spectral comparison of the IEF extract and a s

50 ctrometry (nLC electrospray ionization (ESI) FTICR MS).

51 istry on-line with mass spectrometry, EC/ESI-FTICR MS, of triphenylamine (TPA), which undergoes one-e

52 knowledge for the first time, the use of ESI-FTICR MS and MALDI-FTICR MS is described in a complement

53 l results for both RPLC-ESI-TOF and RPLC-ESI-FTICR MS were similar, with approximately 2000 different

54 n cyclotron resonance mass spectrometer (ESI-FTICR MS).

55 n cyclotron resonance mass spectrometry (ESI-FTICR MS) has demonstrated capabilities for advanced cha

56 cant sensitivity enhancement compared to ESI-FTICR MS.

57 he nonrhizosphere soil (54% of the >2200 ESI-FTICR-MS identified compounds).

58 n cyclotron resonance mass spectrometry (ESI-FTICR-MS) and cyclic voltammetry.

59 n cyclotron resonance mass spectrometry (ESI-FTICR-MS) for achieving the high resolution and ultrasen

60 n cyclotron resonance mass spectrometry (ESI-FTICR-MS) in the negative ion mode with infrared multiph

61 n cyclotron resonance mass spectrometry (ESI-FTICR-MS) spectroscopies show that the association of DO

62 ansform ion cyclotron mass spectrometry (ESI-FTICR-MS) to study the relative stabilities of noncovale

63 al results on the application of SA-TIMS-ExD-FTICR MS to the separation and identification of glycan

64 plex samples, while maintaining the expected FTICR MS resolving power and mass accuracy.

65 h other ionization methods, such as ESI, for FTICR MS studies of NOM.

66 While external calibration for FTICR-MS can result in mass errors of greater than 100 p

67 cation of molecular information derived from FTICR MS.

68 cation of SID for high-throughput studies in FTICR MS.

69 surements will allow significant advances in FTICR-MS research by improving the current understanding

70 in the loss of induced ion image current in FTICR-MS measurements and are normally inseparable durin

71 example of electron capture dissociation in FTICR-MS is presented.

72 This report represents the first online LC-FTICR MS coupling in the field of crude oil analysis.

73 he software and hardware tools for online LC-FTICR MS/MS studies in which a set of initially unidenti

74 on cyclotron resonance mass spectrometry (LC-FTICR-MS), for improved analysis of the amine- and pheno

75 on cyclotron resonance mass spectrometry (LC-FTICR-MS), is described for quantitative profiling of th

76 hese sequential steps was enabled through LC-FTICR-MS of enzyme-bound intermediates and products.

77 LDI FTICR-MS can detect the target lipids in single submilli

78 elected archaeal tetraethers acquired by LDI FTICR-MS are highly correlated with values obtained by c

79 position information retrieved from off-line FTICR-MS, a variety of aliphatic and aromatic carboxylic

80 clotron resonance mass spectrometer (nLC-LTQ-FTICR-MS).

81 cyclotron resonance mass spectrometry (MALDI FTICR MS) in the negative ion mode is described for enha

82 irst time, the use of ESI-FTICR MS and MALDI-FTICR MS is described in a complementary manner with the

83 ed using protein profiles generated by MALDI-FTICR MS.

84 as a new matrix for tissue imaging by MALDI-FTICR MS.

85 Ultrahigh resolution MALDI-FTICR MS allows the measurement of small proteins at iso

86 cyclotron resonance mass spectrometry (MALDI-FTICR MS).

87 Recently, using a MALDI-FTICR-MS platform equipped with a 15 T magnet, we report

88 As a result, CIRCA serves to enable MALDI-FTICR-MS/MS for high-performance proteomics experiments.

89 cyclotron resonance mass spectrometry (MALDI-FTICR-MS).

90 novel MS/MS approach implemented with MALDI-FTICR-MS and specifically intended for enhanced fragment

91 e for thousands of peptides in a single muLC-FTICR-MS experiment.

92 lotron resonance-mass spectrometry (nanoDESI FTICR-MS).

93 of 872 proteins/run from a single 3-h nanoLC/FTICR MS analysis.

94 ere possible because of the mass accuracy of FTICR MS at high field (9.4 T) and the regular mass spac

95 The global increase in the application of FTICR MS to address SOM complexity has highlighted the m

96 The accurate mass capabilities of FTICR MS permitted the nature of the intermediate to be

97 Furthermore, we have exploited the power of FTICR MS to interrogate the quenched covalently bound en

98 The high mass resolving power of FTICR MS was exploited to identify TPB2+ dication in the

99 With the high resolving power of FTICR MS, it was possible to differentiate between batch

100 ution, and high-mass measurement accuracy of FTICR-MS.

101 approaches are essential, the attributes of FTICR-MS are poised to make significant contributions.

102 Even the accurate mass capabilities of FTICR-MS alone cannot unambiguously identify cross-linke

103 ombined with the accurate mass capability of FTICR-MS can help distinguish cross-linking reaction pro

104 he promising advantages of 2D correlation of FTICR-MS data is the ability to associate the variations

105 Spearman's correlation of FTICR-MS peak and PARAFAC component relative intensities

106 FAIMS combined with the high sensitivity of FTICR-MS detection make possible separation of multiple

107 is study show great potential for the use of FTICR-MS as both a rapid method for determining existing

108 important for more efficient utilization of FTICR-MS.

109 Adequacy of the APPI-P FTICR-MS data for the determination of commonly used GDG

110 ties associated with SOM sample preparation, FTICR MS analysis, and mass spectral interpretation.

111 ion cyclotron resonance mass spectrometer (Q-FTICR-MS).

112 good repeatability of ultra-high resolution FTICR-MS, both in terms of m/z and coefficient of variat

113 Using a combination of high-resolution FTICR-MS and timsTOF MSI, we assessed ionization efficie

114 e show the potential of ultrahigh resolution FTICR-MS as a valuable analytical technique for determin

115 Ultrahigh-resolution FTICR-MS measurements provided fully resolved isotopic d

116 work, the advantages of DI-FTICR MS and SFC-FTICR MS proved complementary, and DI was useful to stud

117 nsform ion cyclotron resonance mass spectra (FTICR-MS) of ultrafiltered dissolved organic matter samp

118 m ion cyclotron resonance mass spectrometer (FTICR MS) has been constructed in our laboratory.

119 m ion cyclotron resonance mass spectrometer (FTICR MS) to resolve and identify thousands of peaks fro

120 m-ion cyclotron resonance mass spectrometer (FTICR MS).

121 m ion cyclotron resonance mass spectrometer (FTICR-MS), as well as by offline ultrahigh performance l

122 m ion cyclotron resonance-mass spectrometer (FTICR-MS).

123 ion cyclotron resonance mass spectrometric (FTICR MS) analysis of the relative proportions of post-t

124 m ion cyclotron resonance mass spectrometry (FTICR MS) and a suite of solvents with varying polarity

125 m ion cyclotron resonance mass spectrometry (FTICR MS) and proton nuclear magnetic resonance ((1)H NM

126 m ion cyclotron resonance mass spectrometry (FTICR MS) delivers high resolving power, mass measuremen

127 m ion cyclotron resonance mass spectrometry (FTICR MS) enables the direct characterization of complex

128 m ion cyclotron resonance mass spectrometry (FTICR MS) for the analysis of complex hydrocarbon mixtur

129 m ion cyclotron resonance mass spectrometry (FTICR MS) is the only technique that has sufficient mass

130 m ion cyclotron resonance mass spectrometry (FTICR MS) is used to compare two different batches of Ge

131 m ion cyclotron resonance mass spectrometry (FTICR MS) provides a unique opportunity for molecular an

132 m ion cyclotron resonance mass spectrometry (FTICR MS) provides the resolution and mass accuracy need

133 m ion cyclotron resonance mass spectrometry (FTICR MS) studies of natural organic matter (NOM).

134 m-ion cyclotron resonance mass spectrometry (FTICR MS) to characterize complex humic and fulvic acid

135 m ion cyclotron resonance mass spectrometry (FTICR MS) to demonstrate the potential of this approach

136 m ion cyclotron resonance mass spectrometry (FTICR MS) to elucidate the molecular chemodiversity of f

137 m ion cyclotron resonance mass spectrometry (FTICR MS) was applied to detect isomerization in Abeta p

138 m ion cyclotron resonance mass spectrometry (FTICR MS) with an average mass resolving power of over 5

139 m ion cyclotron resonance mass spectrometry (FTICR MS) with electrospray ionization has advanced the

140 m ion cyclotron resonance mass spectrometry (FTICR MS), based on a prior design by Tolmachev to produ

141 m ion cyclotron resonance mass spectrometry (FTICR MS).

142 m ion cyclotron resonance mass spectrometry (FTICR MS).

143 m ion cyclotron resonance mass spectrometry (FTICR MS).

144 m ion cyclotron resonance mass spectrometry (FTICR MS).

145 m ion cyclotron resonance mass spectrometry (FTICR MS).

146 m ion cyclotron resonance-mass spectrometry (FTICR-MS) along with collisionally activated dissociatio

147 m ion cyclotron resonance mass spectrometry (FTICR-MS) analysis of the AEO fraction in phosphate-bios

148 m ion cyclotron resonance mass spectrometry (FTICR-MS) and a recently developed MS/MS technique terme

149 m ion cyclotron resonance mass spectrometry (FTICR-MS) and mass defect filtering to identify bioaccum

150 m ion cyclotron resonance mass spectrometry (FTICR-MS) dataset, we reveal fundamental scaling pattern

151 m ion cyclotron resonance mass spectrometry (FTICR-MS) has shown great promise to GAG oligosaccharide

152 m ion cyclotron resonance mass spectrometry (FTICR-MS) is complex and the subject of ongoing theoreti

153 m ion cyclotron resonance mass spectrometry (FTICR-MS) is playing an increasing role in the character

154 m ion cyclotron resonance mass spectrometry (FTICR-MS) is utilized in this study to analyze biochar w

155 m ion cyclotron resonance mass spectrometry (FTICR-MS) makes possible lower detection limits, increas

156 m ion cyclotron resonance mass spectrometry (FTICR-MS) of CDA nebularized in the presence of saturati

157 m ion cyclotron resonance mass spectrometry (FTICR-MS) of secondary metabolites, and lipidomics, was

158 m ion cyclotron resonance mass spectrometry (FTICR-MS) poses challenges in molecular formula assignme

159 m ion cyclotron resonance mass spectrometry (FTICR-MS) provides an exceptionally capable platform for

160 m ion cyclotron resonance mass spectrometry (FTICR-MS) revealed the structural details of acidic cons

161 Ion Cyclotron Resonance - Mass Spectrometry (FTICR-MS) to differentiate grapes and corresponding wine

162 m ion cyclotron resonance mass spectrometry (FTICR-MS) to measure changes in the glycerophospholipid

163 m ion cyclotron resonance mass spectrometry (FTICR-MS) utilizing hexapole accumulation and gated trap

164 m ion cyclotron resonance mass spectrometry (FTICR-MS) with absorption mode FT processing in both cas

165 m ion cyclotron resonance mass spectrometry (FTICR-MS).

166 m ion cyclotron resonance mass spectrometry (FTICR-MS).

167 and ultrahigh resolution mass spectrometry (FTICR-MS).

168 m ion cyclotron resonance mass spectrometry (FTICR-MS).

169 r transform ion cyclotron mass spectrometry (FTICR-MS).

170 m ion cyclotron resonance mass spectrometry (FTICR-MS).

171 m ion cyclotron resonance mass spectrometry (FTICR-MS, Bruker Daltonics), in terms of the distributio

172 Within the frame of this study, FTICR-MS along with multivariate statistical analyses co

173 ompounds are traced through natural systems, FTICR-MS remains advantageous.

174 ing a monolithic column interfaced to a 12 T FTICR MS equipped with electron capture dissociation (EC

175 s (i.e., approximately 100 times larger than FTICR MS), corresponding to a sensitivity of approximate

176 Up to 47% of the FTICR-MS signal from MOS extracts can be attributed to f

177 mber of formulas identified and 59% of total FTICR-MS peak intensities, and included significant numb

178 n cyclotron resonance mass spectrometer (UHR FTICR MS) is presented.

179 nents assigned in the excipients batch using FTICR-MS, compared to the numbers previously assigned by

180 e at a subunit interface (active site) using FTICR-MS.

181 nformational/compositional patterns, whereas FTICR MS analysis provides comprehensive heteroatom clas

182 , TOF MS analyses were more effective, while FTICR MS was more effective for the >150-s analysis due

183 MALDI-ISD combined with FTICR MS appears to be a useful method for sequencing of

184 orted use of online quench-flow coupled with FTICR MS.

185 his fully integrated and flexible gTIMS with FTICR MS analysis possesses the potential to significant