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      단백체 분석을 위한 일차원 및 이차원 역상크로마토그래피의 비교 = Comparison of 2-D RP-RP MS/MS with 1-D RP MS/MS for Proteomic Analysis

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      https://www.riss.kr/link?id=A100412917

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      다국어 초록 (Multilingual Abstract) kakao i 다국어 번역

      Single-dimensional (1-D) and two-dimensional (2-D) LC methods were utilized to separate peptides from various sources followed by MS/MS analysis. Two-dimensional ultra-high performance liquid chromatography is a useful tool for proteome analysis, providing a greater peak capacity than 1-D LC. The most popular 2-D LC approach used today for proteomic research combines strong cation exchange and reversed-phase LC. We have evaluated an alternative mode for 2-D LC of peptides using 2-D RP-RP nano UPLC Q-TOF Mass Spectrometry, employing reversed-phase columns in both separation dimensions. As control experiments, we identified 129 proteins in 1-D LC and 322 proteins in 2-D LC from E.coli extract peptides. Furthermore, we applied this method to rat primary hepatocyte and a total of 170 proteins were identified from 1-D LC, and 527 proteins were identified from all 2-D LC system. The in-depth protein profiling established by this 2-D LC MS/MS from rat primary hepatocyte could be a very useful reference for future applications in regards to drug induced liver toxicity.
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      Single-dimensional (1-D) and two-dimensional (2-D) LC methods were utilized to separate peptides from various sources followed by MS/MS analysis. Two-dimensional ultra-high performance liquid chromatography is a useful tool for proteome analysis, prov...

      Single-dimensional (1-D) and two-dimensional (2-D) LC methods were utilized to separate peptides from various sources followed by MS/MS analysis. Two-dimensional ultra-high performance liquid chromatography is a useful tool for proteome analysis, providing a greater peak capacity than 1-D LC. The most popular 2-D LC approach used today for proteomic research combines strong cation exchange and reversed-phase LC. We have evaluated an alternative mode for 2-D LC of peptides using 2-D RP-RP nano UPLC Q-TOF Mass Spectrometry, employing reversed-phase columns in both separation dimensions. As control experiments, we identified 129 proteins in 1-D LC and 322 proteins in 2-D LC from E.coli extract peptides. Furthermore, we applied this method to rat primary hepatocyte and a total of 170 proteins were identified from 1-D LC, and 527 proteins were identified from all 2-D LC system. The in-depth protein profiling established by this 2-D LC MS/MS from rat primary hepatocyte could be a very useful reference for future applications in regards to drug induced liver toxicity.

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      참고문헌 (Reference)

      1 Gilar, M, "Twodimensional separation of peptides using RP-RP-HPLC system with different pH in first and second separation dimensions" 28 : 1694-, 2005

      2 Toll, H, "Separation, detection, and identification of peptides by ion-pair reversed-phase high-performance liquid chromatographyelectrospray ionization mass spectrometry at high and low pH" 1079 : 274-, 2005

      3 Schley, C, "Proteome analysis of Myxococcus xanthus by off-line two-dimensional chromatographic separation using monolithic poly-(styrene-divinylbenzene) columns combined with ion-trap tandem mass spectrometry" 5 : 2760-, 2006

      4 Eriksson, J, "Protein identification in complex mixtures" 4 : 387-, 2005

      5 Omenn, G. S, "Overview of the HUPO plasma proteome project: results from the pilot phase with 35 collaborating laboratories and multiple analytical groups, generating a core dataset of 3020 proteins and a publicly-available database" 5 : 3226-, 2005

      6 Rowe, C, "Network analysis of primary hepatocyte dedifferentiation using a shotgun proteomics approach" 9 : 2658-, 2010

      7 Korolainen, M. A, "Multiplexed proteomic analysis of oxidation and concentrations of cerebrospinal fluid proteins in Alzheimer disease" 53 : 657-, 2007

      8 Washburn, M. P, "Large-scale analysis of the yeast proteome by multidimensional protein identification technology" 19 : 242-, 2001

      9 Beigel, J, "Genomics and proteomics analysis of cultured primary rat hepatocytes" 22 : 171-, 2008

      10 Masuda, J, "Fully automated micro- and nanoscale one- or two-dimensional high-performance liquid chromatography system for liquid chromatography-mass spectrometry compatible with non-volatile salts for ion exchange chromato graphy" 1063 : 57-, 2005

      1 Gilar, M, "Twodimensional separation of peptides using RP-RP-HPLC system with different pH in first and second separation dimensions" 28 : 1694-, 2005

      2 Toll, H, "Separation, detection, and identification of peptides by ion-pair reversed-phase high-performance liquid chromatographyelectrospray ionization mass spectrometry at high and low pH" 1079 : 274-, 2005

      3 Schley, C, "Proteome analysis of Myxococcus xanthus by off-line two-dimensional chromatographic separation using monolithic poly-(styrene-divinylbenzene) columns combined with ion-trap tandem mass spectrometry" 5 : 2760-, 2006

      4 Eriksson, J, "Protein identification in complex mixtures" 4 : 387-, 2005

      5 Omenn, G. S, "Overview of the HUPO plasma proteome project: results from the pilot phase with 35 collaborating laboratories and multiple analytical groups, generating a core dataset of 3020 proteins and a publicly-available database" 5 : 3226-, 2005

      6 Rowe, C, "Network analysis of primary hepatocyte dedifferentiation using a shotgun proteomics approach" 9 : 2658-, 2010

      7 Korolainen, M. A, "Multiplexed proteomic analysis of oxidation and concentrations of cerebrospinal fluid proteins in Alzheimer disease" 53 : 657-, 2007

      8 Washburn, M. P, "Large-scale analysis of the yeast proteome by multidimensional protein identification technology" 19 : 242-, 2001

      9 Beigel, J, "Genomics and proteomics analysis of cultured primary rat hepatocytes" 22 : 171-, 2008

      10 Masuda, J, "Fully automated micro- and nanoscale one- or two-dimensional high-performance liquid chromatography system for liquid chromatography-mass spectrometry compatible with non-volatile salts for ion exchange chromato graphy" 1063 : 57-, 2005

      11 Peng, J, "Evaluation of multidimensional chromatography coupled with tandem mass spectrometry (LC/LC-MS/MS) for largescale protein analysis: the yeast proteome" 2 : 43-, 2003

      12 Nakamura, T, "Evaluation of comprehensive multidimensional separations using reversedphase,reversed-phase liquid chromatography/mass spectrometry for shotgun proteomics" 7 : 1007-, 2008

      13 Figliomeni, M. L, "Ethanol does not increase the hepatotoxicity of cocaine in primary rat hepatocyte culture" 129 : 25-, 1998

      14 Zolotarjova, N, "Differences among techniques for highabundant protein depletion" 5 : 3304-, 2005

      15 Liu, H, "Development of an Automated RP/RP 2D Nano LC/MS Method for Proteomic Analysis"

      16 Echan, L. A, "Depletion of multiple high-abundance proteins improves protein profiling capacities of human serum and plasma" 5 : 3292-, 2005

      17 Dennis, G., Jr, "DAVID: Database for Annotation, Visualization, and Integrated Discovery" 4 : 3-, 2003

      18 Dowell, J. A, "Comparison of two-dimensional fractionation techniques for shotgun proteomics" 80 : 6715-, 2008

      19 Gilar, M, "Comparison of 1-D and 2-D LC MS/MS methods for proteomic analysis of human serum" 30 : 1157-, 2009

      20 Shen, Y, "Automated 20 kpsi RPLC-MS and MS/MS with chromatographic peak capacities of 1000-1500 and capabilities in proteomics and metabolomics" 77 : 3090-, 2005

      21 Bargagli, E, "Analysis of carbonylated proteins in bronchoalveolar lavage of patients with diffuse lung diseases" 185 : 139-, 2007

      22 Wolters, D. A, "An automated multidimensional protein identification technology for shotgun proteomics" 73 : 5683-, 2001

      23 Adkins, J. N, "A proteomic study of the HUPO Plasma Proteome Project's pilot samples using an accurate mass and time tag strategy" 5 : 3454-, 2005

      24 Han, C. L, "A multiplexed quantitative strategy for membrane proteomics: opportunities for mining therapeutic targets for autosomal dominant polycystic kidney disease" 7 : 1983-, 2008

      25 Weatherly, D. B, "A Heuristic method for assigning a false-discovery rate for protein identifications from Mascot database search results" 4 : 762-, 2005

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      연월일 이력구분 이력상세 등재구분
      2027 평가예정 재인증평가 신청대상 (재인증)
      2021-01-01 평가 등재학술지 유지 (재인증) KCI등재
      2018-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2015-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2011-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2009-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2007-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2004-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      2003-01-01 평가 등재후보 1차 PASS (등재후보1차) KCI등재후보
      2002-01-01 평가 등재후보학술지 유지 (등재후보1차) KCI등재후보
      1999-07-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 0.2 0.2 0.22
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.23 0.18 0.403 0.02
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