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. 1997 Oct 1;110(4):379–389. doi: 10.1085/jgp.110.4.379

Table I.

Data from HEK293 Cells Cotransfected with Expression Plasmids Encoding α1, α2δa, and β1a Ca Channel Subunits

α1 construct Ca current density Fast tau ICa Fast tau IBa External solution
pA/pF ms ms
α1C −56 ± 9 (17) 17 ± 2 (14)  88 ± 8 (7) TEAC1
α1C −17 ± 3 (7) 38 ± 6 (7)        — TEAC1
α1C−3′del −68 ± 21 (7) 20 ± 4 (8)  93 ± 21 (6) TEAC1
CSk1 −28 ± 5 (12) 20 ± 1 (11)  57 ± 11 (6) TEAC1
CSk2 −28 ± 11 (8) 35 ± 4 (9) 295 ± 38 (8) TEAC1
CSk2 −20 ± 7 (5) 51 ± 8 (5) 467 ± 107 (4) NaCl
CSk3 −23 ± 6 (9) 31 ± 5 (9) 129 ± 13 (4) TEAC1
CSk3 −45 ± 9 (6) 38 ± 5 (6) 106 ± 22 (3) NaCl
CSk4 −16 ± 3 (10) 70 ± 4 (5)  75 ± 5 (5) TEAC1
CSk4 −13 ± 5 (4) 82 ± 15 (4)  80 ± 10 (4) NaCl
CSk5 −51 ± 12 (8) 32 ± 4 (10)  97 ± 9 (8) TEAC1
CSk5 −17 ± 6 (5) 76 ± 7 (5) 111 ± 6 (7) NaCl
CSk8 −51 ± 12 (8) 23 ± 4 (8) 110 ± 10 (7) TEAC1

The external solution was based upon TEAC1 or NaCl (see materials and methods for compositions). Time constants for inactivation were derived by fitting maximal Ca or Ba currents (i.e., at the peak of the I–V relationship) with one or two exponential functions. Only the fast time constants (fast tau) were analyzed. Currents were evoked by test pulses of 250 or 500 ms, or 1.25 or 5 s, as dictated by the inactivation rate. Mean ± SEM, with the number of cells (n) in parentheses.