Silicon chip-based patch-clamp electrodes integrated with PDMS microfluidics

被引:134
作者
Pantoja, R
Nagarah, JM
Starace, DM
Melosh, NA
Blunck, R
Bezanilla, F
Heath, JR [1 ]
机构
[1] Univ Calif Los Angeles, Sch Med, Dept Biochem & Chem, Calif Nanosyst Inst, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Sch Med, Dept Physiol, Calif Nanosyst Inst, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, Sch Med, Dept Anesthesiol, Calif Nanosyst Inst, Los Angeles, CA 90095 USA
[4] CALTECH, Div Chem & Chem Engn, Pasadena, CA 91125 USA
关键词
silicon microchip; BioMEMS; biosensor; patch-clainp; electrophysiology; biomembranes;
D O I
10.1016/j.bios.2004.02.020
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
We report on a silicon wafer-based device that can be used for recording macroscopic ion channel protein activities across a diverse group of cell-types. Gigaohm seals were achieved for CHO-K1 and RIN m5F cells, and both cell-attached and whole-cell mode configurations were also demonstrated. Two distinct intrinsic potassium ion channels were recorded in whole-cell mode for HIT-T15 and RAW 264.7 cells. Polydimethylsiloxane (PDMS) microfluidics were also coupled with the micromachined silicon chips in order to demonstrate that a single cell could be selectively directed to a micropore, and membrane protein currents could subsequently be recorded. These silicon chip-based devices have significant advantages over traditional micropipette approaches, and may serve as combinatorial tools for investigating membrane biophysics, pharmaceutical screening, and other bio-sensing tasks. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:509 / 517
页数:9
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