Kinase Inhibitor Screening In Self-assembled Human Protein Microarrays

被引:0
|
作者
Festa, Fernanda [1 ,2 ]
Labaer, Joshua [1 ]
机构
[1] Arizona State Univ, Biodesign Inst, Virginia G Piper Ctr Personalized Diagnost, Tempe, AZ 85287 USA
[2] Penn State Univ, Coll Med, Dept Pediat & Biochem Mol Biol, University Pk, PA 16802 USA
来源
关键词
Biochemistry; Issue; 152; self-assembled protein microarrays; drug screening; protein kinase assay; tyrosine kinase inhibitors; high-throughput screening; screen of kinase inhibitors; NAPPA protein microarray; IMATINIB MESYLATE; TYROSINE KINASE;
D O I
10.3791/59886
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The screening of kinase inhibitors is crucial for better understanding properties of a drug and for the identification of potentially new targets with clinical implications. Several methodologies have been reported to accomplish such screening. However, each has its own limitations (e.g., the screening of only ATP analogues, restriction to using purified kinase domains, significant costs associated with testing more than a few kinases at a time, and lack of flexibility in screening protein kinases with novel mutations). Here, a new protocol that overcomes some of these limitations and can be used for the unbiased screening of kinase inhibitors is presented. A strength of this method is its ability to compare the activity of kinase inhibitors across multiple proteins, either between different kinases or different variants of the same kinase. Self-assembled protein microarrays generated through the expression of protein kinases by a human-based in vitro transcription and translation system (IVTT) are employed. The proteins displayed on the microarray are active, allowing for measurement of the effects of kinase inhibitors. The following procedure describes the protocol steps in detail, from the microarray generation and screening to the data analysis.
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页数:11
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