Analysis of Single Channel Currents with a Microprocessor Based Device

1987 ◽  
Vol 42 (3) ◽  
pp. 173-177
Author(s):  
W. Schreibmayer ◽  
E. Hofer ◽  
P. Wolf ◽  
A. Lueger ◽  
H. A. Tritthart

Data evaluation of single channel currents obtained from artificial black lipid membranes and with the patch clamp method is an important part of every single channel study, but it is a time consuming part often exceeding the time for experimentation and recording by far. We describe here a microprocessor based device, which allows the experimentator to analyse in a simple way the distribution of current levels in a single channel trace (amplitude-histogram analysis of single channel currents) either online, or offline. Current levels are sampled at a constant frequency of 6 kHz and the relative frequencies of occurrence of these current levels are displayed as a histogram on the screen of an analog or digital storage oscilloscope. The data reducing algorithm of this analyser eliminates the requirement of large amounts of mass storage that normally is needed for digital amplitude-histogram analysis of single channel recordings. Examples of evaluation for both a voltage operated cation-channel and a blockage of a potas­sium channel by tetraethylammoniumchloride (TEA) are given.

1991 ◽  
Vol 161 (1) ◽  
pp. 455-468
Author(s):  
F. ZUFALL ◽  
H. HATT ◽  
T. A. KEIL

Single-channel patch-clamp techniques were used to identify and characterize a Ca2+-activated nonspecific cation channel (CAN channel) on insect olfactory receptor neurones (ORNs) from antennae of male Antheraea polyphemus. The CAN channel was found both in acutely isolated ORNs from developing pupae and in membrane vesicles from mature ORNs that presumably originated from inner dendritic segments. Amplitude histograms of the CAN single-channel currents presented well-defined peaks corresponding to at least four channel substates each having a conductance of about 16 pS. Simultaneous gating of the substates was achieved by intracellular Ca2+ with an EC50 value of about 80 nmoll−1. Activity of the CAN channel could be blocked by application of amiloride (IC50 <100nmoll−1). Moreover, in the presence of 1μmoll−1 Ca2+, opening of the CAN channel was totally suppressed by 10 μmoll−1 cyclic GMP, whereas ATP (1 mmol l−1) was without effect. We suggest that the CAN channel plays a specific role in modulation of cell excitability and in shaping the voltage response of ORNs.


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