Utility of the hybrid LTQ-FTMS for drug metabolism applications

被引:35
作者
Sanders, Mark
Shipkova, Petia A.
Zhang, Haiying
Warrack, Bethanne M.
机构
[1] Bristol Myers Squibb Co, Pharmaceut Res Inst, Bioanalyt & Discovery Analyt Sci, Lawrenceville, NJ USA
[2] Bristol Myers Squibb Co, Pharmaceut Res Inst, Bioanalyt & Discovery Analyt Sci, Hopewell, NJ USA
关键词
Fourier transform ion cyclotron resonance mass Spectrometry (FTICR); Fourier transform mass Spectrometry (FTMS); orbitrap; linear ion trap; metabolite identification; accurate mass; mass defect filter (MDF); metabonomics;
D O I
10.2174/138920006777697972
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Fourier Transform Ion Cyclotron Mass Spectrometry (FTMS) provides the highest mass accuracy and mass resolving power of the currently available mass spectrometers. One of the main drawbacks in its use for absorption, distribution, metabolism and excretion (ADME) applications has been its incompatibility with standard HPLC columns and flow rates. Hybrid instruments, such as the LTQ-FT, provide the much needed bridge between the excellent performance and capabilities of the FT mass spectrometers and the well-established, tested and validated features of quadrupoles and ion traps. The hybrid instruments are compatible with standard HPLC flow rates, have high-throughput and automation compatibility, and also provide data dependant MSn. The ability to maintain the fidelity of an externally calibrated accurate mass measurement across an HPLC peak, where the analyte concentrations are rapidly changing, is a significant advance for this technology, as is the ability to perform data dependent MS/MS experiments on the chromatographic time scale. The MS and accurate mass capabilities are routinely utilized to rapidly confirm the identification of expected metabolites or to elucidate the structures of unusual or unexpected metabolites. The combination of traditional high-flow chromatography and robust, externally calibrated accurate mass determination for both parent and product ions makes the LTQ-FTMS a very powerful analytical tool for the characterization of metabolites, identification of metabolic soft-spots and for metabonomics studies.
引用
收藏
页码:547 / 555
页数:9
相关论文
共 62 条
[1]  
Aharoni Asaph, 2002, OMICS A Journal of Integrative Biology, V6, P217, DOI 10.1089/15362310260256882
[2]   Design and performance of an ESI interface for selective external ion accumulation coupled to a Fourier transform ion cyclotron mass spectrometer [J].
Belov, ME ;
Nikolaev, EN ;
Anderson, GA ;
Udseth, HR ;
Conrads, TP ;
Veenstra, TD ;
Masselon, CD ;
Gorshkov, MV ;
Smith, RD .
ANALYTICAL CHEMISTRY, 2001, 73 (02) :253-261
[3]   Proteomics by FTICR mass spectrometry: Top down and bottom up [J].
Bogdanov, B ;
Smith, RD .
MASS SPECTROMETRY REVIEWS, 2005, 24 (02) :168-200
[4]   Metabolomics applications of FT-ICR mass spectrometry [J].
Brown, SC ;
Kruppa, G ;
Dasseux, JL .
MASS SPECTROMETRY REVIEWS, 2005, 24 (02) :223-231
[5]   Exact mass measurements using a 7 Tesla Fourier transform ion cyclotron resonance mass spectrometer in a good laboratory practices-regulated environment [J].
Burton, RD ;
Matuszak, KP ;
Watson, CH ;
Eyler, JR .
JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 1999, 10 (12) :1291-1297
[6]  
BUSBY SA, 2004, P 52 ASMS C MASS SPE
[7]   Systematic LC/MS metabolite identification in drug discovery [J].
Clarke, N ;
Rindgen, D ;
Korfmacher, W ;
Cox, K .
ANALYTICAL CHEMISTRY, 2001, 73 (15) :430A-439A
[8]   Micro-high-performance liquid chromatography/Fourier transform mass spectrometry with electron-capture dissociation for the analysis of protein enzymatic digests [J].
Davidson, W ;
Frego, L .
RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 2002, 16 (10) :993-998
[9]   Improved molecular weight-based processing of intact proteins for interrogation by quadrupole-enhanced FT MS/MS [J].
Du, Y ;
Meng, FY ;
Patrie, SM ;
Miller, LM ;
Kelleher, NL .
JOURNAL OF PROTEOME RESEARCH, 2004, 3 (04) :801-806
[10]  
FOSTER LJ, 2004, P 52 ASMS C MASS SPE