Application of ion-sensitive field effect transistors for ion channel screening

被引:19
|
作者
Walsh, Kenneth B. [1 ]
DeRoller, Nicholas [2 ]
Zhu, Yihao [2 ]
Koley, Goutam [2 ]
机构
[1] Univ S Carolina, Sch Med, Dept Pharmacol Physiol & Neurosci, Columbia, SC 29209 USA
[2] Univ S Carolina, Sch Engn, Dept Elect Engn, Columbia, SC 29208 USA
来源
关键词
ISFET; K+ efflux; Screening assay; Cell lines; Ion channel modulators; PROTEIN-KINASE; BK CHANNELS; TECHNOLOGIES; CALCIUM; VOLTAGE; DEVICES; IMPACT; CELLS;
D O I
10.1016/j.bios.2013.11.038
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Cell-based screening assays are now widely used for identifying compounds that serve as ion channel modulators. However, instrumentation for the automated, real-time analysis of ion flux from clonal and primary cells is lacking. This study describes the initial development of an ion-sensitive field effect transistor (ISFET)-based screening assay for the acquisition of K+ efflux data from cells cultured in multi-well plates. Silicon-based K+-sensitive ISFETs were tested for their electrical response to varying concentrations of KCl and were found to display a linear response relationship to KCl in the range of 10 mu M-1 mM. The ISFETs, along with reference electrodes, were inserted into fast-flow chambers containing either human colonic T84 epithelial cells or U251-MG glioma cells. Application of the Ca2+ ionophore A23187 (1 mu M), to activate Ca2+-activated non-selective cation (NSC) channels (T84 cells) and large conductance Ca2+-activated K+ (BK) channels (U251 cells), resulted in time-dependent increases in the extracellular K+ concentration ([K+](o)) as measured with the ISFETs. Treatment of the cells with blockers of either the NSC or BK channels, caused a strong inhibition of the A23187-induced increase in [K+](o). These results were consistent with ion current measurements obtained using the whole-cell arrangement of the patch clamp procedure. In addition, K+ efflux data could be acquired in parallel from multiple cell chambers using the ISFET sensors. Given the non-invasive properties of the probes, the ISFET-based assay should be adaptable for screening ion channels in various cell types. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:448 / 454
页数:7
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