These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
159 related articles for article (PubMed ID: 17249691)
1. Minimizing back exchange in 18O/16O quantitative proteomics experiments by incorporation of immobilized trypsin into the initial digestion step. Sevinsky JR; Brown KJ; Cargile BJ; Bundy JL; Stephenson JL Anal Chem; 2007 Mar; 79(5):2158-62. PubMed ID: 17249691 [TBL] [Abstract][Full Text] [Related]
2. Proteolytic labeling with 18O for comparative proteomics studies: preparation of 18O-labeled peptides and the 18O/16O peptide mixture. Fenselau C; Yao X Methods Mol Biol; 2007; 359():135-42. PubMed ID: 17484115 [TBL] [Abstract][Full Text] [Related]
3. A simple procedure for effective quenching of trypsin activity and prevention of 18O-labeling back-exchange. Petritis BO; Qian WJ; Camp DG; Smith RD J Proteome Res; 2009 May; 8(5):2157-63. PubMed ID: 19222237 [TBL] [Abstract][Full Text] [Related]
4. Quantitative protein analysis using enzymatic [¹⁸O]water labeling. Castillo MJ; Reynolds KJ; Gomes A; Fenselau C; Yao X Curr Protoc Protein Sci; 2014 Apr; 76():23.4.1-23.4.9. PubMed ID: 24692014 [TBL] [Abstract][Full Text] [Related]
5. Production of 18O-single labeled peptide fragments during trypsin digestion of proteins for quantitative proteomics using nanoLC-ESI-MS/MS. Mori M; Abe K; Yamaguchi H; Goto J; Shimada M; Mano N J Proteome Res; 2010 Jul; 9(7):3741-9. PubMed ID: 20496949 [TBL] [Abstract][Full Text] [Related]
6. Trypsin immobilization on hairy polymer chains hybrid magnetic nanoparticles for ultra fast, highly efficient proteome digestion, facile 18O labeling and absolute protein quantification. Qin W; Song Z; Fan C; Zhang W; Cai Y; Zhang Y; Qian X Anal Chem; 2012 Apr; 84(7):3138-44. PubMed ID: 22413971 [TBL] [Abstract][Full Text] [Related]
7. 18O labeling: a tool for proteomics. Stewart II; Thomson T; Figeys D Rapid Commun Mass Spectrom; 2001; 15(24):2456-65. PubMed ID: 11746917 [TBL] [Abstract][Full Text] [Related]
8. Considerations for proteolytic labeling-optimization of 18O incorporation and prohibition of back-exchange. Storms HF; van der Heijden R; Tjaden UR; van der Greef J Rapid Commun Mass Spectrom; 2006; 20(23):3491-7. PubMed ID: 17072904 [TBL] [Abstract][Full Text] [Related]
10. Enhancing the stability of ¹⁸O-labeled peptides through removal of immobilized trypsin by ZipTips. Li MY; Peng F; Zuo JH; Yi H; Tang CE; Li C; Zhang PF; Chen ZC; Xiao ZQ Anal Biochem; 2011 Jan; 408(1):37-45. PubMed ID: 20816659 [TBL] [Abstract][Full Text] [Related]
11. Global differential non-gel proteomics by quantitative and stable labeling of tryptic peptides with oxygen-18. Staes A; Demol H; Van Damme J; Martens L; Vandekerckhove J; Gevaert K J Proteome Res; 2004; 3(4):786-91. PubMed ID: 15359732 [TBL] [Abstract][Full Text] [Related]
12. 18O-labeling quantitative proteomics using an ion trap mass spectrometer. Sakai J; Kojima S; Yanagi K; Kanaoka M Proteomics; 2005 Jan; 5(1):16-23. PubMed ID: 15744833 [TBL] [Abstract][Full Text] [Related]
13. Improved method for differential expression proteomics using trypsin-catalyzed 18O labeling with a correction for labeling efficiency. Ramos-Fernández A; López-Ferrer D; Vázquez J Mol Cell Proteomics; 2007 Jul; 6(7):1274-86. PubMed ID: 17322307 [TBL] [Abstract][Full Text] [Related]
14. Mass spectrum patterns of 18O-tagged peptides labeled by enzyme-catalyzed oxygen exchange. Fernandez-de-Cossio J Anal Chem; 2011 Apr; 83(8):2890-6. PubMed ID: 21417365 [TBL] [Abstract][Full Text] [Related]
15. Minimizing 18O/16O back-exchange in the relative quantification of ribonucleic acids. Castleberry CM; Lilleness K; Baldauff R; Limbach PA J Mass Spectrom; 2009 Aug; 44(8):1195-202. PubMed ID: 19484804 [TBL] [Abstract][Full Text] [Related]
16. Proteolytic 18O-labeling strategies for quantitative proteomics. Miyagi M; Rao KC Mass Spectrom Rev; 2007; 26(1):121-36. PubMed ID: 17086517 [TBL] [Abstract][Full Text] [Related]
17. Trypsin catalyzed 16O-to-18O exchange for comparative proteomics: tandem mass spectrometry comparison using MALDI-TOF, ESI-QTOF, and ESI-ion trap mass spectrometers. Heller M; Mattou H; Menzel C; Yao X J Am Soc Mass Spectrom; 2003 Jul; 14(7):704-18. PubMed ID: 12837592 [TBL] [Abstract][Full Text] [Related]
18. Trypsin is the primary mechanism by which the (18)O isotopic label is lost in quantitative proteomic studies. Angel PM; Orlando R Anal Biochem; 2006 Dec; 359(1):26-34. PubMed ID: 17046705 [TBL] [Abstract][Full Text] [Related]
19. Trypsin-mediated ¹⁸O/¹⁶O labeling for biomarker discovery. Ye X; Chan KC; Prieto DA; Luke BT; Johann DJ; Stockwin LH; Newton DL; Blonder J Methods Mol Biol; 2013; 1002():133-49. PubMed ID: 23625401 [TBL] [Abstract][Full Text] [Related]
20. Proteomic analysis of ductal carcinoma of the breast using laser capture microdissection, LC-MS, and 16O/18O isotopic labeling. Zang L; Palmer Toy D; Hancock WS; Sgroi DC; Karger BL J Proteome Res; 2004; 3(3):604-12. PubMed ID: 15253443 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]