HTPS flow cytometry: A novel platform for automated high throughput drug discovery and characterization

被引:17
作者
Edwards, BS
Kuckuck, FW
Prossnitz, ER
Ransom, JT
Sklar, LA
机构
[1] Univ New Mexico, Hlth Sci Ctr, Cytometry Canc Res & Treatment Ctr, Albuquerque, NM 87131 USA
[2] Univ New Mexico, Hlth Sci Ctr, Dept Pathol, Albuquerque, NM 87131 USA
[3] Univ New Mexico, Hlth Sci Ctr, Canc Res & Treatment Ctr, Canc Res Facil, Albuquerque, NM 87131 USA
[4] Axiom Biotechnol Inc, San Diego, CA USA
关键词
D O I
10.1177/108705710100600204
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The flow cytometer is unique among biomedical analysis instruments because it makes simultaneous and multiple optical measurements on individual cells or particles at high rates. High throughput flow cytometry represents a potentially important multifactorial approach for screening large combinatorial libraries of compounds. Limiting this approach has been the availability of instrumentation acid methods in flow cytometry for automated sample handling on the scale required for drug discovery applications. Here, we describe an automated system in which a novel patented fluidics-based pharmacology platform, the HTPS (High Throughput Pharmacological System), is coupled to a flow cytometer using a recently described plug flow-coupling valve technology. Individual samples are aspirated sequentially from microplate wells and delivered to a flow cytometer for rapid multiparametric analysis. For primacy screening to detect and quantify cell fluorescence in endpoint assays, a high-speed no-wash protocol enabled processing of 9-10 cell samples/min from 96-well microplates, In an alternate primary screening format, soluble receptor ligands were sampled from microplate wells at rates of 3-4 samples/minute and successfully assessed for the ability to elicit intracellular calcium responses. Experiments with fluorescent beads validated the accurate automated production by the HTPS of exponential and linear gradients of soluble compounds. This feature enabled rapid (2- to 3-min) characterization of the intracellular calcium dose response of myeloid cells to formyl peptide as well as the quantitative relationship between formyl peptide receptor occupancy and cell response, HTPS flow cytometry thus represents a powerful high throughput multifactorial approach to increase the efficiency with which novel bioresponse-modifying drugs may be identified and characterized.
引用
收藏
页码:83 / 90
页数:8
相关论文
共 15 条
[1]  
Edwards BS, 1999, CYTOMETRY, V37, P156, DOI 10.1002/(SICI)1097-0320(19991001)37:2<156::AID-CYTO9>3.0.CO
[2]  
2-T
[3]   Undifferentiated U937 cells transfected with chemoattractant receptors: A model system to investigate chemotactic mechanisms and receptor structure/function relationships [J].
Kew, RR ;
Peng, T ;
DiMartino, SJ ;
Madhavan, D ;
Weinman, SJ ;
Cheng, D ;
Prossnitz, ER .
JOURNAL OF LEUKOCYTE BIOLOGY, 1997, 61 (03) :329-337
[4]   FLOW-INJECTION CYTOMETRY - A NEW APPROACH FOR SAMPLE AND SOLUTION HANDLING IN FLOW-CYTOMETRY [J].
LINDBERG, W ;
RUZICKA, J ;
CHRISTIAN, GD .
CYTOMETRY, 1993, 14 (02) :230-236
[5]  
Melamed MR., 1990, FLOW CYTOMETRY SORTI
[6]  
Nolan John P., 1998, P19
[7]   Flow cytometry: a versatile tool for all phases of drug discovery [J].
Nolan, JP ;
Lauer, S ;
Prossnitz, ER ;
Sklar, LA .
DRUG DISCOVERY TODAY, 1999, 4 (04) :173-180
[8]  
OKUN I, 2000, SPIE P, V3924, P88
[9]  
RANSOM JT, 2000, SPIE P, V3921, P90
[10]  
Seamer LC, 1999, CYTOMETRY, V35, P75, DOI 10.1002/(SICI)1097-0320(19990101)35:1<75::AID-CYTO10>3.0.CO