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Volumn 20, Issue 11, 2009, Pages 2124-2134

Shifting Unoccupied Spectral Space in Mass Spectrum of Peptide Fragment Ions

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID RESIDUES; INTERFERING IONS; LABORATORY EXPERIMENTS; MASS DEFECT; MASS SPECTRA; MASS-TO-CHARGE RATIO; N-BUTANOL; PEPTIDE FRAGMENTS; PHOSPHOTYROSINE; SCALING FACTORS; SIDE-CHAIN; SPECTRAL SPACES; THEORETICAL CALCULATIONS;

EID: 70349767010     PISSN: 10440305     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jasms.2009.07.005     Document Type: Article
Times cited : (7)

References (36)
  • 2
    • 0033405276 scopus 로고    scopus 로고
    • Modeling peptide mass fingerprinting data using the atomic composition of peptides
    • Gay S., Binz P.A., Hochstrasser D.F., and Appel R.D. Modeling peptide mass fingerprinting data using the atomic composition of peptides. Electrophoresis 20 (1999) 3527-3534
    • (1999) Electrophoresis , vol.20 , pp. 3527-3534
    • Gay, S.1    Binz, P.A.2    Hochstrasser, D.F.3    Appel, R.D.4
  • 3
    • 0033671142 scopus 로고    scopus 로고
    • The information encrypted in accurate peptide masses-improved protein identification and assistance in glycopeptide identification and characterization
    • Lehmann W.D., Bohne A., and von Der Lieth C.-W. The information encrypted in accurate peptide masses-improved protein identification and assistance in glycopeptide identification and characterization. J. Mass Spectrom 35 (2000) 1335-1341
    • (2000) J. Mass Spectrom , vol.35 , pp. 1335-1341
    • Lehmann, W.D.1    Bohne, A.2    von Der Lieth, C.-W.3
  • 4
    • 33645526350 scopus 로고    scopus 로고
    • Accessible proteomics space and its implications for peak capacity for zero-, one-, and two-dimensional separations coupled with FT-ICR and TOF mass spectrometry
    • Frahm J.L., Howard B.E., Heber S., and Muddiman D.C. Accessible proteomics space and its implications for peak capacity for zero-, one-, and two-dimensional separations coupled with FT-ICR and TOF mass spectrometry. J. Mass Spectrom 41 (2006) 281-288
    • (2006) J. Mass Spectrom , vol.41 , pp. 281-288
    • Frahm, J.L.1    Howard, B.E.2    Heber, S.3    Muddiman, D.C.4
  • 5
    • 33646555091 scopus 로고    scopus 로고
    • Enhanced peptide mass fingerprinting through high mass accuracy: Exclusion of non-peptide signals based on residual mass
    • Dodds E.D., An H.J., Hagerman P.J., and Lebrilla C.B. Enhanced peptide mass fingerprinting through high mass accuracy: Exclusion of non-peptide signals based on residual mass. J. Proteome Res 5 (2006) 1195-1203
    • (2006) J. Proteome Res , vol.5 , pp. 1195-1203
    • Dodds, E.D.1    An, H.J.2    Hagerman, P.J.3    Lebrilla, C.B.4
  • 6
    • 34147173417 scopus 로고    scopus 로고
    • On the proper use of mass accuracy in proteomics
    • Zubarev R., and Mann M. On the proper use of mass accuracy in proteomics. Mol. Cell. Proteom 6 (2007) 377-381
    • (2007) Mol. Cell. Proteom , vol.6 , pp. 377-381
    • Zubarev, R.1    Mann, M.2
  • 7
    • 0042386237 scopus 로고    scopus 로고
    • Iterative data analysis is the key for exhaustive analysis of peptide mass fingerprints from proteins separated by two-dimensional electrophoresis
    • Schmidt F., Schmid M., Jungblut P.R., Mattow J., Facius A., and Pleissner K.P. Iterative data analysis is the key for exhaustive analysis of peptide mass fingerprints from proteins separated by two-dimensional electrophoresis. J. Am. Soc. Mass Spectrom 14 (2003) 943-956
    • (2003) J. Am. Soc. Mass Spectrom , vol.14 , pp. 943-956
    • Schmidt, F.1    Schmid, M.2    Jungblut, P.R.3    Mattow, J.4    Facius, A.5    Pleissner, K.P.6
  • 8
    • 58149209843 scopus 로고
    • Determination of monoisotopic masses and ion populations for large biomolecules from resolved isotopic distributions
    • Senko M.W., Beu S.C., and McLafferty F.W. Determination of monoisotopic masses and ion populations for large biomolecules from resolved isotopic distributions. J. Am. Soc. Mass Spectrom 6 (1995) 229-233
    • (1995) J. Am. Soc. Mass Spectrom , vol.6 , pp. 229-233
    • Senko, M.W.1    Beu, S.C.2    McLafferty, F.W.3
  • 9
    • 54749157078 scopus 로고    scopus 로고
    • Averagine-scaling analysis and fragment ion mass defect labeling in peptide mass spectrometry
    • Yao X., Diego P., Ramos A.A., and Shi Y. Averagine-scaling analysis and fragment ion mass defect labeling in peptide mass spectrometry. Anal. Chem 80 (2008) 7383-7391
    • (2008) Anal. Chem , vol.80 , pp. 7383-7391
    • Yao, X.1    Diego, P.2    Ramos, A.A.3    Shi, Y.4
  • 10
    • 33646751578 scopus 로고    scopus 로고
    • Mass defect labeling of cysteine for improving peptide assignment in shotgun proteomic analyses
    • Hernandez H., Niehauser S., Boltz S.A., Gawandi V., Phillips R.S., and Amster I.J. Mass defect labeling of cysteine for improving peptide assignment in shotgun proteomic analyses. Anal. Chem 78 (2006) 3417-3423
    • (2006) Anal. Chem , vol.78 , pp. 3417-3423
    • Hernandez, H.1    Niehauser, S.2    Boltz, S.A.3    Gawandi, V.4    Phillips, R.S.5    Amster, I.J.6
  • 12
    • 14644392991 scopus 로고    scopus 로고
    • Isotope-differentiated binding energy shift tags (IDBEST) for improved targeted biomarker discovery and validation
    • Hall M.P., and Schneider L.V. Isotope-differentiated binding energy shift tags (IDBEST) for improved targeted biomarker discovery and validation. Expert Rev. Proteom 1 (2004) 421-431
    • (2004) Expert Rev. Proteom , vol.1 , pp. 421-431
    • Hall, M.P.1    Schneider, L.V.2
  • 13
    • 10044293272 scopus 로고    scopus 로고
    • Use of performic acid oxidation to expand the mass distribution of tryptic peptides
    • Matthiesen R., Bauw G., and Welinder K.G. Use of performic acid oxidation to expand the mass distribution of tryptic peptides. Anal. Chem 76 (2004) 6848-6852
    • (2004) Anal. Chem , vol.76 , pp. 6848-6852
    • Matthiesen, R.1    Bauw, G.2    Welinder, K.G.3
  • 15
    • 0036374351 scopus 로고    scopus 로고
    • Use of matrix clusters and trypsin autolysis fragments as mass calibrants in matrix-assisted laser desorption/ionization time-of-flight mass spectrometry
    • Harris W.A., Janecki D.J., and Reilly J.P. Use of matrix clusters and trypsin autolysis fragments as mass calibrants in matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. Rapid Commun. Mass Spectrom 16 (2002) 1714-1722
    • (2002) Rapid Commun. Mass Spectrom , vol.16 , pp. 1714-1722
    • Harris, W.A.1    Janecki, D.J.2    Reilly, J.P.3
  • 16
    • 49549094510 scopus 로고    scopus 로고
    • Application of fractional mass for the identification of peptide-oligonucleotide cross-links by mass spectrometry
    • Pourshahian S., and Limbach P.A. Application of fractional mass for the identification of peptide-oligonucleotide cross-links by mass spectrometry. J. Mass Spectrom 43 (2008) 1081-1088
    • (2008) J. Mass Spectrom , vol.43 , pp. 1081-1088
    • Pourshahian, S.1    Limbach, P.A.2
  • 17
    • 36148937543 scopus 로고    scopus 로고
    • Systematic characterization of high mass accuracy influence on false discovery and probability scoring in peptide mass fingerprinting
    • Dodds E.D., Clowers B.H., Hagerman P.J., and Lebrilla C.B. Systematic characterization of high mass accuracy influence on false discovery and probability scoring in peptide mass fingerprinting. Anal. Biochem 372 (2008) 156-166
    • (2008) Anal. Biochem , vol.372 , pp. 156-166
    • Dodds, E.D.1    Clowers, B.H.2    Hagerman, P.J.3    Lebrilla, C.B.4
  • 18
    • 0035298820 scopus 로고    scopus 로고
    • Detection of tyrosine phosphorylated peptides by precursor ion scanning quadrupole TOF mass spectrometry in positive ion mode
    • Steen H., Küster B., Fernandez M., Pandey A., and Mann M. Detection of tyrosine phosphorylated peptides by precursor ion scanning quadrupole TOF mass spectrometry in positive ion mode. Anal. Chem 73 (2001) 1440-1448
    • (2001) Anal. Chem , vol.73 , pp. 1440-1448
    • Steen, H.1    Küster, B.2    Fernandez, M.3    Pandey, A.4    Mann, M.5
  • 19
    • 0034909215 scopus 로고    scopus 로고
    • Quadrupole time-of-flight versus triple-quadrupole mass spectrometry for the determination of phosphopeptides by precursor ion scanning
    • Steen H., Küster B., and Mann M. Quadrupole time-of-flight versus triple-quadrupole mass spectrometry for the determination of phosphopeptides by precursor ion scanning. J. Mass Spectrom 36 (2001) 782-790
    • (2001) J. Mass Spectrom , vol.36 , pp. 782-790
    • Steen, H.1    Küster, B.2    Mann, M.3
  • 20
    • 0037940028 scopus 로고    scopus 로고
    • Analysis of protein tyrosine phosphorylation by nanoelectrospray ionization high-resolution tandem mass spectrometry and tyrosine-targeted product ion scanning
    • Salek M., Alonso A., Pipkorn R., and Lehmann W.D. Analysis of protein tyrosine phosphorylation by nanoelectrospray ionization high-resolution tandem mass spectrometry and tyrosine-targeted product ion scanning. Anal. Chem 75 (2003) 2724-2729
    • (2003) Anal. Chem , vol.75 , pp. 2724-2729
    • Salek, M.1    Alonso, A.2    Pipkorn, R.3    Lehmann, W.D.4
  • 21
    • 36448983248 scopus 로고    scopus 로고
    • Oxygen isotopic substitution of peptidyl phosphates for modification-specific mass spectrometry
    • Shi Y., and Yao X. Oxygen isotopic substitution of peptidyl phosphates for modification-specific mass spectrometry. Anal. Chem 79 (2007) 8454-8462
    • (2007) Anal. Chem , vol.79 , pp. 8454-8462
    • Shi, Y.1    Yao, X.2
  • 22
    • 54749085464 scopus 로고    scopus 로고
    • Cyclophosphoramidate ion as mass defect marker for efficient detection of protein serine phosphorylation
    • Shi Y., Bajrami B., Morton M., and Yao X. Cyclophosphoramidate ion as mass defect marker for efficient detection of protein serine phosphorylation. Anal. Chem 80 (2008) 7614-7623
    • (2008) Anal. Chem , vol.80 , pp. 7614-7623
    • Shi, Y.1    Bajrami, B.2    Morton, M.3    Yao, X.4
  • 23
    • 65249137629 scopus 로고    scopus 로고
    • Global and site-specific quantitative phosphoproteomics: Principles and applications
    • Macek B., Mann M., and Olsen J.V. Global and site-specific quantitative phosphoproteomics: Principles and applications. Annu. Rev. Pharmacol. Toxicol 49 (2009) 199-221
    • (2009) Annu. Rev. Pharmacol. Toxicol , vol.49 , pp. 199-221
    • Macek, B.1    Mann, M.2    Olsen, J.V.3
  • 24
    • 0001261561 scopus 로고
    • Mass scale based on CH2 = 14.0000 for high-resolution mass spectrometry of organic compounds
    • Kendrick E. Mass scale based on CH2 = 14.0000 for high-resolution mass spectrometry of organic compounds. Anal. Chem 35 (1963) 2146-2154
    • (1963) Anal. Chem , vol.35 , pp. 2146-2154
    • Kendrick, E.1
  • 25
    • 0035472251 scopus 로고    scopus 로고
    • Kendrick mass defect spectrum: A compact visual analysis for ultrahigh-resolution broadband mass spectra
    • Hughey C.A., Hendrickson C.L., Rodgers R.P., Marshall A.G., and Qian K. Kendrick mass defect spectrum: A compact visual analysis for ultrahigh-resolution broadband mass spectra. Anal. Chem 73 (2001) 4676-4681
    • (2001) Anal. Chem , vol.73 , pp. 4676-4681
    • Hughey, C.A.1    Hendrickson, C.L.2    Rodgers, R.P.3    Marshall, A.G.4    Qian, K.5
  • 26
    • 0038047154 scopus 로고    scopus 로고
    • Shotgun collision-induced dissociation of peptides using a time of flight mass analyzer
    • Purvine S., Eppel J.-T., Yi E.C., and Goodlett D.R. Shotgun collision-induced dissociation of peptides using a time of flight mass analyzer. Proteomics 3 (2003) 847-850
    • (2003) Proteomics , vol.3 , pp. 847-850
    • Purvine, S.1    Eppel, J.-T.2    Yi, E.C.3    Goodlett, D.R.4
  • 28
    • 33748765574 scopus 로고    scopus 로고
    • Tandem parallel fragmentation of peptides for mass spectrometry
    • Ramos A.A., Yang H., Rosen L.E., and Yao X. Tandem parallel fragmentation of peptides for mass spectrometry. Anal. Chem 78 (2006) 6391-6397
    • (2006) Anal. Chem , vol.78 , pp. 6391-6397
    • Ramos, A.A.1    Yang, H.2    Rosen, L.E.3    Yao, X.4
  • 30
    • 30544452187 scopus 로고    scopus 로고
    • Mapping posttranslational modifications of proteins by MS-based selective detection: Application to phosphoproteomics
    • Carr S.A., Annan R.S., and Huddleston M.J. Mapping posttranslational modifications of proteins by MS-based selective detection: Application to phosphoproteomics. Methods Enzymol 405 (2005) 82-115
    • (2005) Methods Enzymol , vol.405 , pp. 82-115
    • Carr, S.A.1    Annan, R.S.2    Huddleston, M.J.3
  • 32
    • 34250172066 scopus 로고    scopus 로고
    • Achieving augmented limits of detection for peptides with hydrophobic alkyl tags
    • Frahm J.L., Bori I.D., Comins D.L., Hawkridge A.M., and Muddiman D.C. Achieving augmented limits of detection for peptides with hydrophobic alkyl tags. Anal. Chem 79 (2007) 3989-3995
    • (2007) Anal. Chem , vol.79 , pp. 3989-3995
    • Frahm, J.L.1    Bori, I.D.2    Comins, D.L.3    Hawkridge, A.M.4    Muddiman, D.C.5
  • 33
    • 39549091726 scopus 로고    scopus 로고
    • Synthesis, characterization, and application of iodoacetamide derivatives utilized for the ALiPHAT strategy
    • Williams Jr. D.K., Meadows C.W., Bori I.D., Hawkridge A.M., Comins D.L., and Muddiman D.C. Synthesis, characterization, and application of iodoacetamide derivatives utilized for the ALiPHAT strategy. J. Am. Chem. Soc 130 (2008) 2122-2123
    • (2008) J. Am. Chem. Soc , vol.130 , pp. 2122-2123
    • Williams Jr., D.K.1    Meadows, C.W.2    Bori, I.D.3    Hawkridge, A.M.4    Comins, D.L.5    Muddiman, D.C.6
  • 34
    • 33745268913 scopus 로고    scopus 로고
    • Enhancing electrospray ionization efficiency of peptides by derivatization
    • Mirzaei H., and Regnier F. Enhancing electrospray ionization efficiency of peptides by derivatization. Anal. Chem 78 (2006) 4175-4183
    • (2006) Anal. Chem , vol.78 , pp. 4175-4183
    • Mirzaei, H.1    Regnier, F.2
  • 35
    • 33745686436 scopus 로고    scopus 로고
    • Probabilistic enrichment of phosphopeptides by their mass defect
    • Bruce C., Shifman M.A., Miller P., and Gulcicek E.E. Probabilistic enrichment of phosphopeptides by their mass defect. Anal. Chem 78 (2006) 4374-4382
    • (2006) Anal. Chem , vol.78 , pp. 4374-4382
    • Bruce, C.1    Shifman, M.A.2    Miller, P.3    Gulcicek, E.E.4
  • 36
    • 68049098188 scopus 로고    scopus 로고
    • Passive and active fragment Ion mass defect labeling: Distinct proteomics potential of iodine-based reagents
    • E-pub June 29, 2009
    • Shi Y., Bajrami B., and Yao X. Passive and active fragment Ion mass defect labeling: Distinct proteomics potential of iodine-based reagents. Anal. Chem (2009) E-pub June 29, 2009
    • (2009) Anal. Chem
    • Shi, Y.1    Bajrami, B.2    Yao, X.3


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