AN ICONOGRAPHIC PROGRAM FOR COMPUTER-CONTROLLED WHOLE-CELL VOLTAGE-CLAMP EXPERIMENTS

被引:9
作者
BUDAI, D
KEHL, LJ
POLIAC, GI
WILCOX, GL
机构
[1] Department of Pharmacology, University of Minnesota, Medical School, Minneapolis
关键词
MACINTOSH; LABVIEW; 2; VOLTAGE CLAMP; CULTURED NEURON; MEMBRANE CURRENT; LEAK SUBTRACTION; CURRENT-VOLTAGE RELATIONSHIP;
D O I
10.1016/S0165-0270(05)80008-1
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A Macintosh-based system is described for performing instrument control, data acquisition and storage operations in single-electrode whole-cell voltage clamp experiments. The system consists of a commercially available voltage clamp amplifier, multifunction input/output (I/O) board, graphical programming language (LabVIEW 2) and custom built 'virtual instrument' (VI). The I/O board is capable of fast (up to 110 ksample/s) multichannel analog-to-digital (A/D) conversion with 12-bit resolution. It can control the gain settings of the clamp unit through digital I/O lines and generate the P/N leak subtraction protocol to eliminate the linear portion of capacitive currents using analog output voltages and gating pulses. Complete voltage clamp protocols can be implemented using the on-screen front panel controls of the VI. It enables the user to visualize the acquired data, to graph sets of current-voltage (I-V) relations or to fit single-exponential functions to one current trace. To evaluate the adequacy of whole-cell recording, the total membrane capacitance (C(m)), the series resistance (R(s)) and the time constant (tau(c)) of the decay of the capacitive current are calculated using the single-exponential function fit to the data. The system is particularly well suited to the study of large quantities of transmembrane I-V relationships. Source code for the crucial elements of the VI as well as sample recordings from a cultured spinal cord neuron, illustrating system operation, are presented.
引用
收藏
页码:65 / 74
页数:10
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