期刊文献+

特发性高草酸尿症大鼠肝脏差异蛋白质的筛选

Differentially expressed proteins in the liver of rats with idiopathic hyperoxaluria
原文传递
导出
摘要 目的寻找特发性高草酸尿症大鼠肝脏组织差异表达的蛋白质。方法取3只雄性特发性高草酸尿症大鼠和3只正常对照雄性大鼠,分别取其肝脏组织约300mg后提取其中的总蛋白。以荧光差异显示凝胶电泳(DIGE)技术分离肝脏中的全部蛋白质,用基质辅助激光解吸电离飞行时间质谱技术(MALDI—TOFMS)和DeCyderTMv6.5软件进行蛋白质的分析和鉴定。结果总共筛选出21个差异表达蛋白质点,其中11个蛋白质点在特发性高草酸尿症组表达上调,10个蛋白质点下调。最终有18个差异蛋白质点被鉴定确认。结论筛选出的这些差异蛋白质可能与特发性高草酸尿症有关。 Objective To investigate differentially expressed proteins in the liver of rats with idiopathic hyperoxaluria. Methods three male rats with idiopathic hyperoxaluria served as study group, and 3 normal ones as controls. The liver of rats with idiopathic hyperoxaluria and the normal liver tissue were examined by two-dimensional gel electrophoresis (2-DE) after labeled with CyDye DIGE Fluors Cy3, Cy5 and Cy2. Intensity changes of protein spots detected with statistical significance were identified by MALDI- TOF MS. Results Intensity changes of 21 spots were detected with statistical significance. Eleven protein spots of them were up-regulated, and the remaining 10 down-regulated. And 18 of them were identified by MALDI-TOF MS successfully. Conclusion DIGE is a useful technique for differential expressed proteins screening and analysis in the liver of rats with idiopathic hyperoxaluria. Pdia3, ALDH, TTR, etc. differently expressed proteins may be key proteins for idiopathic hyperoxaluria.
出处 《中华实验外科杂志》 CAS CSCD 北大核心 2009年第6期783-785,共3页 Chinese Journal of Experimental Surgery
关键词 特发性高草酸尿症 差异蛋白质 蛋白质组学 肝脏 Idiopathic hyperoxaluria Differentially expressed proteins Proteomics Liver
  • 相关文献

参考文献9

  • 1Sutton RA, Walker VR. Enteric and mild hyperoxaluria. Miner Electrolyte Metab, 1994,20:352-360.
  • 2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
  • 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张曦,郭树忠,张琳西,潘阳林,武丽华.增生性瘢痕表皮细胞差异蛋白的初步分析[J].中华实验外科杂志,2005,22(12):1565-1567. 被引量:2
  • 5张春芳,陈主初,郭海周,张恒,肖志强,陈胜喜.缺血预处理对兔肺缺血再灌注性损伤的蛋白质组学研究[J].中华实验外科杂志,2005,22(11):1376-1377. 被引量:4
  • 6Nemere I, Safford SE, Rohe B, et al. Identification and characterization of 1,25D3-membrane-associated rapid response, steroid ( 1,25D3- MARRS) binding protein. J Steroid Biochem Mol Biol,2004,89-90: 281-285.
  • 7Primm TP, Gilbert HF. Hormone binding by protein disulfide isomerase, a high capacity hormone reservoir of the endoplasmic reticulum. J Biol Chem,2001,276:281-286.
  • 8Larsson B, Nemere L Effect of growth and maturation on membrane-initiated actions of 1,25-dihydroxyvitamin D3-Ⅱ : calcium transport, receptor kinetics, and signal transduction in intestine of female chickens. J Cell Bioehem,2003,90:901-913.
  • 9Veena CK, Josephine A, Preetha SP, et al. Mitochondrial dysfunction in an animal model of hyperoxaluria:a prophylactic approach with fucoidan. Eur J Pharmacol,2008 ,579 :330-336.

二级参考文献51

  • 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张春芳,陈胜喜,罗万俊.缺血预处理对猪肺隔离药物灌注肺损伤的保护作用[J].中华实验外科杂志,2004,21(10):1253-1254. 被引量:6
  • 3刘博,黄志强,周宁新,肖雪媛,刘丹慧,何大澄.肝癌细胞系SMMC7721蛋白质组学初步分析[J].中华实验外科杂志,2004,21(12):1439-1440. 被引量:10
  • 4张春芳,陈胜喜,郭海周,罗万俊.缺血预处理对猪肺缺血再灌注性损伤的保护机制[J].中南大学学报(医学版),2005,30(1):64-67. 被引量:8
  • 5Le Naour F. Contribution of proteomics to tumor immunology. Proteomics, 2001, 1:1295-1320.
  • 6Hanash SM, Bobek MP, Rickman DS, et al.Integrating cancer genornics and proteomics in the post-genome era. Proteornics, 2002,2: 69-75.
  • 7Lawrie LC, FothergiU JE, Murray GI. Spot the differences: proteomics in cancer research. Lncet Oncol, 2001, 2: 270-277.
  • 8Kuster B, Mortensen P, Andersen JS, et al.Mass spectrometry allows direct identification of proteins in large genomes. Proteomics, 2001, 1 : 641-650.
  • 9Challdey 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.
  • 10Mann M, Hendrickson RC, Pandey A. Analysis of proteomes by mass spectrometry.Annu Rev Biochem, 2001, 70:437-473.

共引文献14

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