The automation of a commercial Fourier transform mass spectrometer to provide a quick and robust method for determining exact mass for the synthetic chemist

被引:11
作者
Dykes, S [1 ]
Fancy, SA [1 ]
Perkins, GL [1 ]
Pullen, FS [1 ]
机构
[1] Pfizer Ltd, Global Res & Dev, Sandwich CT13 9NJ, Kent, England
关键词
FT-ICR; FT-MS; automation; high throughput; drug discovery; exact mass; accuracy; precision;
D O I
10.1255/ejms.532
中图分类号
O64 [物理化学(理论化学)、化学物理学]; O56 [分子物理学、原子物理学];
学科分类号
070203 ; 070304 ; 081704 ; 1406 ;
摘要
Automation of a commercially available Fourier transform ion cyclotron resonance (FTICR) mass spectrometer for the routine analysis of the synthetic products from high-speed chemistry is described. The automation includes software written by the instrument manufacturer as well as in-house-developed software that allows electronic submission of samples by the chemist and e-mailing of results back to the chemist. The use of samples of relatively high concentration (approx. 1 mg mL(-1)) is possible due to the protocol that has been developed, which includes dilution by the autosampler during sample injection. Though high concentrations are used for speed and convenience, the amount of sample consumed is still small at approx. 15 mug per injection. The results from this method have been shown to be both accurate (typical error range-2.29 to 2.36 ppm, average error 1.07 ppm) and precise (standard deviation of the order of 0.3 ppm). The system is capable of analysing up to 800 samples per 24 hours. As high-speed chemistry becomes more highly utilised within Pfizer Discovery, the number of samples requiring accurate mass analysis will rise but the method we have described will prevent high-resolution mass spectrometry becoming the bottleneck in new chemical entity production. The accuracy and precision demonstrated by this method allows high confidence levels in assigned molecular formulae for expected compounds and reduces the number of possible formulae to consider when working with a compound that is not the desired product of a given reaction.
引用
收藏
页码:73 / 80
页数:8
相关论文
共 39 条
[21]   INTERPRETING MASS-SPECTRA OF MULTIPLY CHARGED IONS [J].
MANN, M ;
MENG, CK ;
FENN, JB .
ANALYTICAL CHEMISTRY, 1989, 61 (15) :1702-1708
[22]  
Marshall AG, 1998, MASS SPECTROM REV, V17, P1, DOI 10.1002/(SICI)1098-2787(1998)17:1<1::AID-MAS1>3.0.CO
[23]  
2-K
[24]   Sodium trifluoroacetate as a tune/calibration compound for positive- and negative-ion electrospray ionization mass spectrometry in the mass range of 100-4000 Da [J].
Moini, M ;
Jones, BL ;
Rogers, RM ;
Jiang, LF .
JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 1998, 9 (09) :977-980
[25]  
MORRIS M, 1998, NIPPON IYO MASU SUPE, V23, P113
[26]   Automated high resolution mass spectrometry for the synthetic chemist [J].
Perkins, G ;
Pullen, F ;
Thompson, C .
JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 1999, 10 (06) :546-551
[27]   Gas phase salt clusters from electrosprayed alkaline earth colloids [J].
Pope, RM ;
Shen, NZ ;
Nicoll, J ;
Tarnawiecki, B ;
Dejsupa, C ;
Dearden, DV .
INTERNATIONAL JOURNAL OF MASS SPECTROMETRY AND ION PROCESSES, 1997, 162 (1-3) :107-119
[28]   External accumulation of ions for enhanced electrospray ionization Fourier transform ion cyclotron resonance mass spectrometry [J].
Senko, MW ;
Hendrickson, CL ;
Emmett, MR ;
Shi, SDH ;
Marshall, AG .
JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 1997, 8 (09) :970-976
[29]   Counting individual sulfur atoms in a protein by ultrahigh-resolution Fourier transform ion cyclotron resonance mass spectrometry: Experimental resolution of isotopic fine structure in proteins [J].
Shi, SDH ;
Hendrickson, CL ;
Marshall, AG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (20) :11532-11537
[30]  
Speir JP, 2000, RAPID COMMUN MASS SP, V14, P1937, DOI 10.1002/1097-0231(20001030)14:20<1937::AID-RCM115>3.0.CO