期刊文献+

人胆汁蛋白质组双向荧光差异凝胶电泳图谱的建立与差异分析 被引量:8

Comparative proteomics analysis of human bile using two.dimensional differential in-gel electrophorisis
原文传递
导出
摘要 目的建立人胆汁蛋A质组双向荧光差异凝胶电泳分析流程用于胆汁比较蛋A质组学研究。方法实验组与对照组样本各6例,分别取自于胆管癌及胆总管结石病例。样本经纯化处理及定量后,分别标记不同的荧光染料后进行双向电泳与差异分析。结果两组样本均获得高分辨力的双向电泳图谱;各标记蛋白质点的荧光强度与蛋A表达量呈线性关系;实验组与对照组间共筛选出55个差异表达蛋白,其表达量两组间相差1.5倍以上,t检验有统计学意义(P〈0.05)。结论建立了基于双向荧光差异凝胶电泳基础上的胆汁比较蛋白质组学的分析流程。 Objective To establish a two-dimensional differential in-gel electrophorisis process for comparative proteomic analysis of human bile. Methods Bile fluid was obtained from 12 patients with obstructive jaundice (each 6 cases of eholangiocarcinoma and choledocholith). The unfractionated bile fluid was performed sonication and ultracentrifugation to remove the cellular debris and Nucleic Acid as a crude separation. Commercial kits Cleanascite and microcon were adopted to remove the abundant lipid and salt. After quantify by BCA Kit, concentrated and purified samples were labeled with three different CyDyes including one internal standard, and separated with 2-D DIGE in triplicate experiments. Biological variations of the level of protein expression were analyzed with DeCyder software and evaluated for reproducibility and statistical significance. Results Common gel artifacts can be reduced by above mentioned samples treatment method and high resolution bihary 2-D DIGE maps can be obtained ; the fluorescence intensity of separated protein spots have a line relationship with the level of their protein expression; 55 matched protein spots with statistical variance of two groups were detected (t-test, P 〈 0.05). Conclusion An ideal, sample preparation strategy and optimized 2-D DIGE analysis process for human bile were established.
出处 《中华实验外科杂志》 CAS CSCD 北大核心 2008年第4期466-468,共3页 Chinese Journal of Experimental Surgery
基金 国家高新技术研究发展计划(863)项目(2002AA241061)
关键词 蛋白质组 胆汁 双向荧光差异凝胶电泳 Proteome Bile Fluorescence two-dimensional difference gel electrophoresis
  • 相关文献

参考文献7

  • 1Marouga R, David S,Hawkins E, The development of the DIGE system: 2D fluorescence difference gel analysis technology. Anal Bioanal Chem ,2005,382:669-678.
  • 2Veenstra TD, Conrads TP, Hood BL, et al. Biomarkers: mining the biofluid proteome. Mol Cell Proteomics,2005,4:409-418.
  • 3蒋业贵,李兆申.蛋白质组学在肿瘤研究中的应用进展[J].中华实验外科杂志,2003,20(11):1053-1054. 被引量:6
  • 4罗小云,吴庆华.不同样品制备方法对血浆双向凝胶电泳图谱的影响[J].中华实验外科杂志,2007,24(2):140-141. 被引量:3
  • 5Huang HL, Stasyk T, Morandell S, eta!. Biomarker discovery in breast cancer serum using 2-D differential gel electrophoresis/MALDI-TOF/ TOF and data validation by routine clinical assays. Electrophoresis, 2006,27 : 1641-1650.
  • 6Kristiansen TZ, Bunkenborg J, Gronborg M, et al. A proteomic Analysis of Human Bile. Mol Cell Proteomics,2004,3: 715-728.
  • 7Koopmann J,Thμluvath PJ,Zahurak ML, et al. Mac-2-binding protein is a diagnostic marker for biliary tract carcinoma. Cancer, 2004,101 : 1609-1615.

二级参考文献25

  • 1王建东,徐迎新,李荣,刘斯奇.血浆蛋白质组研究进展[J].中华实验外科杂志,2004,21(9):1151-1152. 被引量:7
  • 2王建东,任艳,夏季,宋旭华,刘斯奇,李荣,徐迎新.小鼠血浆去除白蛋白前后的双向凝胶电泳分析[J].中华实验外科杂志,2004,21(11):1374-1375. 被引量:5
  • 3徐迎新,宁宁.蛋白质组学在实验外科中的应用前景[J].中华实验外科杂志,2006,23(4):517-519. 被引量:10
  • 4Le Naour F. Contribution of proteomics to tumor immunology. Proteomics, 2001, 1:1295-1320.
  • 5Hanash SM, Bobek MP, Rickman DS, et al.Integrating cancer genornics and proteomics in the post-genome era. Proteornics, 2002,2: 69-75.
  • 6Lawrie LC, FothergiU JE, Murray GI. Spot the differences: proteomics in cancer research. Lncet Oncol, 2001, 2: 270-277.
  • 7Kuster B, Mortensen P, Andersen JS, et al.Mass spectrometry allows direct identification of proteins in large genomes. Proteomics, 2001, 1 : 641-650.
  • 8Challdey RJ, Burlingame AL. Identification of GlcNA cylation sites of peptides and alpha-erystallin using Q-TOF mass spectrometry. J Am So: Mass Spectrom, 2001, 12;1106-1113.
  • 9Mann M, Hendrickson RC, Pandey A. Analysis of proteomes by mass spectrometry.Annu Rev Biochem, 2001, 70:437-473.
  • 10Zhou H, Ranish JA, Aebersold R, et al.Quantitative proteome analysis by solidphase isotope tagging and mass spectrometry. Nat Biotechnol, 2002, 20 : 512-515.

共引文献7

同被引文献35

引证文献8

二级引证文献11

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部