We studied the effects of trypsin on L-type calcium current in the A7r5 smooth muscle cell line. Intracellular dialysis with trypsin increased the whole-cell current up to fivefold. The effect was concentration dependent, and was prevented by soybean trypsin inhibitor. Ensemble analysis indicated an increase in the number of functional channels, and possibly a smaller increase in the open probability, with no change in the single channel current. The shape of the current-voltage curve was unaffected. Trypsin also nearly eliminated inactivation of currents carried by Ba2+, but had little or no effect on the rapid inactivation process in Ca2+, This indicates that trypsin removes voltage-dependent but not Ca(2+)-dependent inactivation, suggesting the existence of distinct protein domains for these two mechanisms of calcium channel inactivation.
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1 December 1991
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December 01 1991
Calcium currents in the A7r5 smooth muscle-derived cell line. Increase in current and selective removal of voltage-dependent inactivation by intracellular trypsin.
C A Obejero-Paz,
C A Obejero-Paz
Department of Physiology and Biophysics, Case Western Reserve University, Cleveland, Ohio 44106.
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S W Jones,
S W Jones
Department of Physiology and Biophysics, Case Western Reserve University, Cleveland, Ohio 44106.
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A Scarpa
A Scarpa
Department of Physiology and Biophysics, Case Western Reserve University, Cleveland, Ohio 44106.
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C A Obejero-Paz
,
S W Jones
,
A Scarpa
Department of Physiology and Biophysics, Case Western Reserve University, Cleveland, Ohio 44106.
Online ISSN: 1540-7748
Print ISSN: 0022-1295
J Gen Physiol (1991) 98 (6): 1127–1140.
Citation
C A Obejero-Paz, S W Jones, A Scarpa; Calcium currents in the A7r5 smooth muscle-derived cell line. Increase in current and selective removal of voltage-dependent inactivation by intracellular trypsin.. J Gen Physiol 1 December 1991; 98 (6): 1127–1140. doi: https://doi.org/10.1085/jgp.98.6.1127
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Calcium currents in the A7r5 smooth muscle-derived cell line. Calcium-dependent and voltage-dependent inactivation.
J Gen Physiol (November,1991)
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