Applications of pulsed ultrafiltration-mass spectrometry

被引:82
作者
Johnson, BM [1 ]
Nikolic, D [1 ]
van Breemen, RB [1 ]
机构
[1] Univ Illinois, Coll Pharm, Dept Med Chem & Pharmacognosy, Chicago, IL 60612 USA
关键词
pulsed ultrafiltration-mass spectrometry; high-throughput screening; drug development; ligand-receptor binding;
D O I
10.1002/mas.10020
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
Pulsed ultrafiltration-mass spectrometry (PUF-MS) is a method with a variety of uses for the discovery and development of biologically active small molecules, including the screening of combinatorial libraries and natural product extracts for biologically active compounds, investigation of thermodynamic and kinetic ligand-receptor binding parameters, high-throughput metabolic screening, and the screening of combinatorial libraries and botanical extracts for electrophilic metabolites. Solution-phase ligand-screening assays that use pulsed ultrafiltration-mass spectrometry are useful for "reverse pharmocology" studies in which a macromolecular receptor of interest has been isolated, but ligands for the receptor are needed. Protein-binding studies that involve pulsed ultrafiltration can be used to rapidly determine classical binding parameters for interactions between a macromolecular receptor and a compound of interest. Metabolic screening assays can identify substrates for cytochromes P450, and should be capable of characterizing phase I metabolites with a throughput of at least 60 compounds/hr Pulsed ultrafiltration can also be used in conjunction with LC-MS-MS to screen mixtures for compounds that might be activated metabolically to electrophilic quinoid and epoxide metabolites by cytochrome P450; that screening can provide early warning of compounds likely to be toxic when administered in large doses. The combination of pulsed-ultrafiltration extraction and mass spectrometric detection provides the sensitivity and selectivity necessary to characterize compounds present at low concentrations in complex chemical mixtures, and is applicable to the analysis of biologically active compounds,from combinatorial libraries and botanical extracts. (C) 2002 Wiley Periodicals, Inc.
引用
收藏
页码:76 / 86
页数:11
相关论文
共 31 条
  • [1] Evaluation of a micro volume pulsed ultrafiltration cell for screening ligands in non-covalent complexes
    Beverly, MB
    West, P
    Julian, RK
    [J]. COMBINATORIAL CHEMISTRY & HIGH THROUGHPUT SCREENING, 2002, 5 (01) : 65 - 73
  • [2] Caldwell GW, 1999, COMB CHEM HIGH T SCR, V2, P39
  • [3] Pulsed ultrafiltration characterization of binding - I. A new method
    Chen, CJ
    Chen, S
    Woodbury, CP
    Venton, DL
    [J]. ANALYTICAL BIOCHEMISTRY, 1998, 261 (02) : 164 - 182
  • [4] Biochemistry of cyclooxygenase (COX)-2 inhibitors and molecular pathology of COX-2 in neoplasia
    Fosslien, E
    [J]. CRITICAL REVIEWS IN CLINICAL LABORATORY SCIENCES, 2000, 37 (05) : 431 - 502
  • [5] Conformationally restricted analogues of trimethoprim: 2,6-diamino-8-substituted purines as potential dihydrofolate reductase inhibitors from Pneumocystis carinii and Toxoplasma gondii
    Gangjee, A
    Vasudevan, A
    Queener, SF
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 1997, 40 (19) : 3032 - 3039
  • [6] Gu CG, 1999, COMB CHEM HIGH T SCR, V2, P353
  • [7] Screening botanical extracts for quinoid metabolites
    Johnson, BM
    Bolton, JL
    van Breemen, RB
    [J]. CHEMICAL RESEARCH IN TOXICOLOGY, 2001, 14 (11) : 1546 - 1551
  • [8] Kuhnz W, 1998, DRUG METAB DISPOS, V26, P1120
  • [9] Evaluation of estrogenic activity of plant extracts for the potential treatment of menopausal symptoms
    Liu, JH
    Burdette, JE
    Xu, HY
    Gu, CG
    van Breemen, RB
    Bhat, KPL
    Booth, N
    Constantinou, AI
    Pezzuto, JM
    Fong, HHS
    Farnsworth, NR
    Bolton, JL
    [J]. JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2001, 49 (05) : 2472 - 2479
  • [10] Masferrer JL, 2000, CANCER RES, V60, P1306