A Flexible Multiwell Format for Immunofluorescence Screening Microscopy of Small-Molecule Inhibitors

被引:2
|
作者
Scholz, Anne-Kathrin [1 ]
Klebl, Bert M. [2 ]
Morkel, Markus [3 ]
Lehrach, Hans [1 ]
Dahl, Andreas [1 ]
Lange, Bodo M. H. [1 ]
机构
[1] Max Planck Inst Mol Genet, Dept Vertebrate Genom, D-14195 Berlin, Germany
[2] GPC Biotech AG, Planegg Martinsried, Germany
[3] Max Planck Inst Mol Genet, Dept Dev Genet, D-14195 Berlin, Germany
关键词
AURORA KINASE INHIBITOR; CELL-CYCLE; B KINASE; A KINASE; IN-VIVO; P-TEFB; FLAVOPIRIDOL; VX-680; CARCINOMA; APOPTOSIS;
D O I
10.1089/adt.2009.0260
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Large-scale screens in mammalian cells demand for flexible high-throughput screening platforms that allow to analyze cellular traits on a genome-wide level or to identify small-molecule inhibitors (SMIs) from complex compound libraries. In this study we developed and tested high-density cell arrays made out of polydimethylsiloxane (PDMS) that support cell growth directly on standard glass microscope objective slides. We analyzed the effect of 3 reference inhibitors (MLN-8054, VX-680, and flavopiridol) and 4 exploratory, cell permeable small-molecule kinase inhibitors (two benzothiophene-based and two 4-amino-6-arylpyrimidine-based compounds) on different cell lines, using prototype 5 x 5 and 9 x 9 array carpets. We found that high-density PDMS cell arrays support growth of a broad range of cell types, are well suited for compound screens, and are compatible with high-content screening platforms. This novel array format is of particular advantage for compound screening to identify SMIs, when a combination of flexibility with respect to culture volume, well density, and high-resolution imaging is required. In addition, we demonstrated the suitability of this format for reverse transfection and siRNA experiments.
引用
收藏
页码:571 / 580
页数:10
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