期刊文献+

稀土金属元素标记行为考察 被引量:1

The Labeling Behavior Study of Rare Earth Elements
下载PDF
导出
摘要 稀土金属元素因其与双功能试剂的螯合效率高、对肽段的反相色谱行为和质谱的离子化效率影响小、检测背景低,以及过量的金属离子在检测时不会产生干扰等优点,近年来在生物标记结合质谱定量分析研究领域引起了关注。选取稀土金属中单同位素铽(Tb)、钇(Y)、铥(Tm)、钬(Ho)和镥(Lu)5种元素,通过双功能试剂二乙三胺五乙酸双酸酐(DTPA双酸酐)对合成肽段及蛋白质酶切产物标记的过程进行研究,包括对标记条件进行优化,对该质量标签的色谱行为和共洗脱、标记稳定性、离子交换、动态范围、质谱检测限等现象进行考察。结果表明:铥和钬两元素结合效率最高,分别达到了92.5%和89.9%;稳定性考察结果表明,质量标签在4℃下放置一周仍可检测到95%,若将标记好的标签用于定量研究,则放置时间不能超过两周;多金属标记质量标签可以共洗脱;两种金属浓度差不超过6倍时,由离子抑制带来的影响较小;离子交换结果表明,只有很少部分发生了离子交换,对标记实验没有影响。 Rare earth element combined with mass spectrometry has received extensive attention in recent years because of their high chelating efficiency, chromatographic behavior, ionization efficiency, low background and no interference of excessive metal ions. Monoiso- topic elements of terbium (Tb), yttrium (Y), thulium (Tm), holmium (Ho) and lutetium (Lu) were selected as model in this research, and the synthesis of peptides and digestion products from proteins through the bifunctional reagent DTPA double anhydride was investigated. The labeling conditions were optimized, followed by the examination of chromatographic behavior, co-elution, stability, ion replacement, dynamic range and mass detection limits. The results show that thulium and holmium have the best binding efficiency of 92.5% and 89.9%, respectively. Stability test results show that 95% of the quality tagshave been detected in a week when stored at 4 ℃. Better linear relationship can be gotten when the concentration of metal particles within 6 times. The ion exchange results show that only a small part of the ion exchange takes place, and it has no effect on the labeling experiments.
出处 《质谱学报》 EI CAS CSCD 北大核心 2014年第5期427-437,共11页 Journal of Chinese Mass Spectrometry Society
关键词 稀土金属 质量标签 基质辅助激光解吸电离-飞行时间质谱(MALDI-TOF MS) rare earth metal protein quantification matrix-assisted laser desorption-ionization-time of flight mass spectrometry(MALDI-TOF MS)
  • 相关文献

参考文献22

  • 1GEVAERT K, IMPENS F, GHESQUIIRE B, et al. Stable isotopic labeling in proteomics [J]. J Pro- teomies, 2008, 8(23/24): 4 873-4 885.
  • 2李伟.iTRAQ多重化学标记串联质谱技术在比较蛋白质组学中的应用[J].生命的化学,2006,26(5):453-456. 被引量:8
  • 3DESOUZA L, DIEHL G, RODRIGUES M J, et al. Search for cancer markers from endometrial tissues using differentially labeled tags iTRAQ and clCAT with multidimensional liquid chromatography and tandem mass spectrometry[J]. Journal of Pro- teome Research, 2005, 4(2): 377-386.
  • 4ZHANG G A, SPELLMAN D S, SKOLNIK E Y, et al. Quantitative phosphotyrosine proteomics of EphB2 signaling by stable isotope labeling with amino acids in cell culture (SILAC) [J]. Journal of Proteome Research, 2006,5(3) .. 581-588.
  • 5钱林艺,应万涛,刘新,卢庄,蔡耘,何建勇,钱小红.^(18)O稳定同位素标记定量蛋白质组研究技术的建立与优化[J].分析化学,2007,35(2):161-165. 被引量:9
  • 6WHETSTONE P A, BUTLIN N G, CORNEIL- LIE T M, et al. Element-coded affinity tags for peptides and proteins [J]. Bioconjugate Chem, 2004, 15(1).. 3-6.
  • 7LIU H L, ZHANG Y J, WANG J L, et al. Me- thod for quantitative proteomics research by using metal element chelated tags coupled with mass spectrometry[J]. Anal Chem, 2006, 78(18): 6 614-6 621.
  • 8AN N, MEHDI M. Analysis of major protein- protein and protein-metal complexes of crythro- cytes directly from cell lysate utilizing capillary electrophoresis mass spectrometry [ J ]. AnalChem, 2008, 80(18): 7 169-7 173.
  • 9LOO J A. Probing protein metal ion interactions by electrospray ionization mass spectrometry gnolase and nucleocapsid protein[J]. International Journal of Mass Spectrometry, 2001, 204(1/2/ 3) : 113-123.
  • 10CHRISTOPHER A B, JOE S, SEUNG G K, et al. Directing noble metal ion chemistry within a de- signed ferritin protein[J]. Biochemistry, 2008, 47(48): 12 729-12 739.

二级参考文献63

  • 1黄海涛,许桦林.蛋白质组学技术在消化疾病研究中的应用[J].临床消化病杂志,2006,18(2):127-128. 被引量:2
  • 2李伟.iTRAQ多重化学标记串联质谱技术在比较蛋白质组学中的应用[J].生命的化学,2006,26(5):453-456. 被引量:8
  • 3赵丽艳,周春喜,张养军,蔡耘,钱小红.基于生物质谱技术的磺酸化修饰策略及其在蛋白质组学中的应用[J].质谱学报,2007,28(3):185-192. 被引量:3
  • 4ZHANG G, SPELLMAN D, SKOLNIK E, et al. Quantitative phosphotyrosine proteomics of EphB2 signaling by stable isotope labeling with amino acids in cell culture (SILAC)[J]. Journal of Proteome Research, 2006, 5: 581-588.
  • 5LIU H, ZHANG Y, WANG J, et al. Method for quantitative proteomics research by using metal element chelated tags coupled with mass spectrometry [ J ]. Anal Chem, 2006, 78: 6 614-6 621.
  • 6OU K, KESUMA D, GANESAN K, et al. Quantitative profiling of drug-associated proteomic alterations by combined 2-nitrobenzenesulfenyl chloride (NBS) isotope labeling and 2DE/MS identification[J]. Journal of Proteome Research, 2006, 5:2 194-2 206.
  • 7BREDEMEYER A, LEWIS R, MALONE J, et al. A proteomic approach for the discovery of protease substrates[J].Proceedings of the National Academy of Sciences, 2004, 101(32): 11 785-11 790.
  • 8WANG J, GUTIERREZ P, EDWARDS N, et al. Integration of ^18O labeling and solution isoelectrie focusing in a shotgun analysis of mitochondrial proteins[J]. Journal of Proteome Research, 2007, 6: 4 601-4 607.
  • 9LIU H, ZHANG Y, MENG L, et al. Non-gelbased dual ^18O labeling quantitative proteomies strategy[J]. Anal Chem, 2007, 79:7 700-7 707.
  • 10MIYAGI M, SEKHAR R. Proteolytic ^18O-labeling strategies for quantitantive proteomics [J]. Mass Spectrometry Reviews, 2007, 26 : 121-136.

共引文献18

同被引文献30

  • 1邸丽娟,张旭初,张春丽,王荣福.RGD肽类肿瘤受体显像剂的研究进展[J].标记免疫分析与临床,2007,14(1):58-61. 被引量:8
  • 2Lee S,Xie J, Chen X. Chem. Rev.,2010,110(5) : 3087-3111.
  • 3Kerr T J, McLean J A. Chem. Commun.,2010, 46(30) : 5479-5481.
  • 4Ang C Y, Tan S Y, Zhao Y. Org. Biomol. Chem.,2014,12(27) : 4776-4806.
  • 5Von Wallbrunn A, Holtke C,Ziihlsdorf M, Heindel W, Schafers M,Bremer C. Eur. J. Nucl. Med. MoL Imaging, 2007,34(5) : 745-754.
  • 6Shiba K. Chem. Soc. Rev.,2010,39( 1) : 117-126.
  • 7Gygi S P, Rist B, Gerber S A, Turecek F, Gelb M H,Aebersold R. Nat. Biotechnol. , 1999,17(10) : 994-999.
  • 8Yao X, Freas A, Ramirez J, Demirev P A, Fenselau C. Anal. Chem.,2001,73(13) : 2836-2842.
  • 9Ong S E, Blagoev B, Kratchmarova I,Kristensen D B, Steen H, Pandey A, Mann M. Mol. Cell. Proteom.,2002, 1(5): 376-386.
  • 10Ross P L,Huang Y N, Marchese J N, Williamson B, Parker K, Hattan S,Khainovski N, Pillai S,Dey S, Daniels S, Purkayastha S, Juhasz P, Martin S, Bartlet-Jones M, He F, Jacobson A, Pappin D J. Mol. Cell. Proteom.,2004, 3(12) : 1154-1169.

引证文献1

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