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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

25 DAPPI FTICR MS results agree with bulk elemental composition a

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

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

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

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

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

31 bound calmodulin dimers were observed by ESI FTICR MS.

32 mponents of complex mixtures by negative ESI FTICR MS.

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

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

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

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

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

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

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

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

41 cant sensitivity enhancement compared to ESI-FTICR MS.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

89 important for more efficient utilization of FTICR-MS.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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