Application of high-throughput affinity-selection mass spectrometry for screening of chemical compound libraries in lead discovery

被引:14
作者
Zehender, Hartmut [1 ]
Mayr, Lorenz M. [1 ]
机构
[1] Novartis Inst BioMed Res, CPC LFP BCS, CH-4002 Basel, Switzerland
关键词
affinity-selection; assay technology; chemical binders; high-throughput screening; label-free; mass spectrometry; primary assay;
D O I
10.1517/17460441.2.2.285
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
High-throughput screening of chemical libraries for compounds that interfere with a particular molecular target is among the most powerful methodologies applied in lead discovery at present. In this review, the authors describe a label-free, homogeneous, affinity-selection-based technology developed at Novartis, termed SpeedScreen, which is compared with similar technologies used for high-throughput screening in the pharmaceutical and biotechnology industries. The focus at present of SpeedScreen is twofold: first, this technology is applied to orphan genomic targets and to those targets that are non-tractable by a functional assay; second, this technology is applied complementary to the well-established traditional methodologies for the screening of molecular targets. In summary, the authors discuss the value of affinity-selection-based high-throughput screening as a complementary technology to the common functional screening platforms and the benefits as well as the limitations of this new technology are outlined.
引用
收藏
页码:285 / 294
页数:10
相关论文
共 12 条
[1]   A general technique to rank protein-ligand binding affinities and determine allosteric versus direct binding site competition in compound mixtures [J].
Annis, DA ;
Nazef, N ;
Chuang, CC ;
Scott, MP ;
Nash, HM .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (47) :15495-15503
[2]   An affinity selection-mass spectrometry method for the identification of small molecule ligands from self-encoded combinatorial libraries -: Discovery of a novel antagonist of E-coli dihydrofolate reductase [J].
Annis, DA ;
Athanasopoulos, J ;
Curran, PJ ;
Felsch, JS ;
Kalghatgi, K ;
Lee, WH ;
Nash, HM ;
Orminati, JPA ;
Rosner, KE ;
Shipps, GW ;
Thaddupathy, GRA ;
Tyler, AN ;
Vilenchik, L ;
Wagner, CR ;
Wintner, EA .
INTERNATIONAL JOURNAL OF MASS SPECTROMETRY, 2004, 238 (02) :77-83
[3]   A chemoinformatics analysis of hit lists obtained from high-throughput affinity-selection screening [J].
Brown, N ;
Zehender, H ;
Azzaoui, K ;
Schuffenhauer, A ;
Mayr, LM ;
Jacoby, E .
JOURNAL OF BIOMOLECULAR SCREENING, 2006, 11 (02) :123-130
[4]   An ultraefficient affinity-based high-throughout screening process: Application to bacterial cell wall biosynthesis enzyme MurF [J].
Comess, Kenneth M. ;
Schurdak, Mark E. ;
Voorbach, Martin J. ;
Coen, Michael ;
Trumbull, Jonathan D. ;
Yang, Houjun ;
Gao, Lan ;
Tang, Hua ;
Cheng, Xueheng ;
Lerner, Claude G. ;
McCall, Owen ;
Burns, David J. ;
Beutel, Bruce A. .
JOURNAL OF BIOMOLECULAR SCREENING, 2006, 11 (07) :743-754
[5]   Kinase drug discovery by affinity selection/mass spectrometry (ASMS): Application to DNA damage checkpoint kinase Chk1 [J].
Comess, Kenneth M. ;
Trumbull, Jonathan D. ;
Park, Chang ;
Chen, Zehan ;
Judge, Russell A. ;
Voorbach, Martin J. ;
Coen, Michael ;
Gao, Lan ;
Tang, Hua ;
Kovar, Peter ;
Cheng, Xueheng ;
Schurdak, Mark E. ;
Zhang, Haiying ;
Sowin, Tom ;
Burns, David J. .
JOURNAL OF BIOMOLECULAR SCREENING, 2006, 11 (07) :755-764
[6]  
MAYR LM, 2006, EUR PHARM REV, V4, P30
[7]   SpeedScreen: label-free liquid chromatography-mass spectrometry-based high-throughput screening for the discovery of orphan protein ligands [J].
Muckenschnabel, I ;
Falchetto, R ;
Mayr, LM ;
Filipuzzi, I .
ANALYTICAL BIOCHEMISTRY, 2004, 324 (02) :241-249
[8]   Frontal affinity chromatography with MS detection (FAC-MS) in drug discovery [J].
Slon-Usakiewicz, JJ ;
Ng, W ;
Dai, JR ;
Pasternak, A ;
Redden, PR .
DRUG DISCOVERY TODAY, 2005, 10 (06) :409-416
[9]   The sequence of the human genome [J].
Venter, JC ;
Adams, MD ;
Myers, EW ;
Li, PW ;
Mural, RJ ;
Sutton, GG ;
Smith, HO ;
Yandell, M ;
Evans, CA ;
Holt, RA ;
Gocayne, JD ;
Amanatides, P ;
Ballew, RM ;
Huson, DH ;
Wortman, JR ;
Zhang, Q ;
Kodira, CD ;
Zheng, XQH ;
Chen, L ;
Skupski, M ;
Subramanian, G ;
Thomas, PD ;
Zhang, JH ;
Miklos, GLG ;
Nelson, C ;
Broder, S ;
Clark, AG ;
Nadeau, C ;
McKusick, VA ;
Zinder, N ;
Levine, AJ ;
Roberts, RJ ;
Simon, M ;
Slayman, C ;
Hunkapiller, M ;
Bolanos, R ;
Delcher, A ;
Dew, I ;
Fasulo, D ;
Flanigan, M ;
Florea, L ;
Halpern, A ;
Hannenhalli, S ;
Kravitz, S ;
Levy, S ;
Mobarry, C ;
Reinert, K ;
Remington, K ;
Abu-Threideh, J ;
Beasley, E .
SCIENCE, 2001, 291 (5507) :1304-+
[10]  
Wabnitz PA, 2002, RAPID COMMUN MASS SP, V16, P85