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On-line parallel reversed phase two-dimensional liquid chromatography for high-throughput analysis of complex proteomic samples 被引量:2

On-line parallel reversed phase two-dimensional liquid chromatography for high-throughput analysis of complex proteomic samples
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摘要 A comprehensive two-dimensional liquid chromatographic system (2D SCX/RP) is con- structed with a 10-port-2-way valve using strong cation exchange chromatography (Hypersil SCX, 100 mm×4.6 mm I.D.) followed by reversed phase chromatography (Hypersil BDS C18, 15 mm×4.6 mm I.D.) to separate the complex peptides from globin peptic hydrolysate. After the sample was loaded on the SCX column, the phosphate buffer (pH 4.0) was used to elute the peptides. Then, elutes flowed through the interface and the peptides focused on the head of the trapping columns (Hypersil BDS C18, 15 mm×4.6 mm I.D.) but salt passed into the waste. After the valve was switched, the samples were flushed with a backward flow into the RP analytical column. The peptides on the SCX were eluted with 12 discontinuous steps linearly increasing salt concentrations. The peptides enriched on the trapping column were desalted and separated by the RP columns. The resolution and the resolved peaks of the 2D SCX/RP system were greatly increased and the total peak capacity reached as high as 2280. A comprehensive two-dimensional liquid chromatographic system (2D SCX/RP) is con- structed with a 10-port-2-way valve using strong cation exchange chromatography (Hypersil SCX, 100 mm×4.6 mm I.D.) followed by reversed phase chromatography (Hypersil BDS C18, 15 mm×4.6 mm I.D.) to separate the complex peptides from globin peptic hydrolysate. After the sample was loaded on the SCX column, the phosphate buffer (pH 4.0) was used to elute the peptides. Then, elutes flowed through the interface and the peptides focused on the head of the trapping columns (Hypersil BDS C18, 15 mm×4.6 mm I.D.) but salt passed into the waste. After the valve was switched, the samples were flushed with a backward flow into the RP analytical column. The peptides on the SCX were eluted with 12 discontinuous steps linearly increasing salt concentrations. The peptides enriched on the trapping column were desalted and separated by the RP columns. The resolution and the resolved peaks of the 2D SCX/RP system were greatly increased and the total peak capacity reached as high as 2280.
出处 《Science China Chemistry》 SCIE EI CAS 2006年第6期527-533,共7页 中国科学(化学英文版)
基金 Financial support from the National Natural Science Foundation of China (Grant Nos. 20175029 and 20375040) is gratefully acknowledged.
关键词 two-dimensional liquid chromatography interface TRAPPING column proteomics globin. two-dimensional liquid chromatography, interface, trapping column, proteomics, globin.
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  • 1[1]Venter J C, Adams M D, Myers E W, Li P W, Mural R J, Sutton G G , Smith H O, Yandell M, Evans C A, Holl R A, Gocayne J D, et al. Science, 2001, 291: 1304
  • 2[2]International Human Genome Sequencing Consortium. Nature, 2001, 409: 860
  • 3[3]Haynes P A, Gygi S P, Figeys D, Aebersold R. Electrophoresis, 1998, 19(11): 1862
  • 4[4]Pandey A, Podtelejnikov A, Blagoev B, Bustelo X, Mann M, Lodish H. Proc Natl Acad Sci USA, 2000, 97: 179
  • 5[5]O'Farrell P H. J Biol Chem, 1975, 250: 4007
  • 6[6]Celis J E, Gesser B, Dejgaard K, Honore B, Leffers H, Madsen P, Andersen A, Basse B, Celis A, Lauridsen J B. Int J Dev Biol, 1989, 33: 407
  • 7[7]Gygi S P, Corthals G L, Zhang Y, Rochon Y, Aebersold R. Proc Natl Acad Sci USA, 2000, 15: 9390
  • 8[8]Fey S J, Larsen P M. Curr Opin Chem Biol, 2001, 5: 26
  • 9[9]Lilley K S, Razzaq A, Dupree P. Curr Opin Chem Biol, 2002, 6: 46
  • 10[10]Kvasnicka F. http://www.sciencedirect.com. J Chromatogr B Available online 2 December 2002

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  • 1王智聪,张庆合,张维冰,李彤,赵中一.全二维液相色谱(IEC/RP)的构建与评价[J].高等学校化学学报,2005,26(3):426-429. 被引量:8
  • 2王智聪,张庆合,赵中一,张维冰,李彤.二维液相色谱切换技术及其应用[J].分析化学,2005,33(5):722-728. 被引量:20
  • 3Davis M T,Beierle J,Bures E T,et al.Automated LC-LC-MS-MS platform using binary ion-exchange and gradient reversed-phase chromatography for improved proteomic analyses.J Chromatogr B,2001,752:281-291
  • 4Fenn J B,Mann M,Meng C K,et al.Electrospray ionization for mass spectrometry of large biomoleculars.Science,1989,246:64-71
  • 5Wilm M,Shevchenko A,Houthaeve T,et al.Femtomole sequenceing of proteins from polyacrylamide gels bye nanoelectrospray mass-spectrometry.Nature,1996,379:466-469
  • 6Giddings J C.Two dimensional separations:concept and promise.Anal Chem,1984,56:1258A-1270A
  • 7Giddings J C.Concepts and comparisons in multidimensional chromatography.J High Resolut Chromatogr,1987,10:319-323
  • 8Cortes H J.Multidimensional chromatography techniques and applications[M].New York:Marcel dekker,Inc,1990
  • 9Regnier F,Amini A,Chakraborty A,et al.Multidimensional chromatography and the signature peptide approach to proteomics.LC-GC,2001,19:200-213
  • 10Yang C,Liu H C,Yang Q,et al.On-line hyphenation of capillary isoelectric focusing and capillary gel electrophoresis by a dialysis interface.Anal Chem,2003,75:215-218

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