Figure 3.
Figure 3. Effects of redox status on permeability. (A) Single PSAC recording on an infected RBC in solution A with 1 mM DTE in the bath and pipette. Seal resistance equal to 230 GΩ; Vm equal to -100 mV; scale bar 2 pA/100 ms. Additional analyses revealed unchanged single-channel chord conductance, voltage dependence, and open/closed dwell-time distributions (not shown). (B) Osmotic lysis of infected cells in sorbitol lysis solution with (red curve) or without (black) 1 mM DTE. Increasing the DTE concentration to 50 mM or adding preincubation with DTE also had no effect; similar results were obtained with the 8 parasite isolates listed in “Results” and in 14C-sorbitol uptake studies (not shown). (C) Osmotic lysis of uninfected RBCs in sorbitol lysis solution after preincubation with (red curve) or without (black curve) 1 mM t-butyl hydroperoxide for 15 minutes with a 2.5-hour postincubation period at 37°C, as in Huber et al.10 Increasing the postincubation period to 24 hours also had no effect (not shown). Although the transmittance values are presented in arbitrary units, their scaling is conserved in panels B and C so that %T equal to 80 corresponds to complete osmotic lysis.

Effects of redox status on permeability. (A) Single PSAC recording on an infected RBC in solution A with 1 mM DTE in the bath and pipette. Seal resistance equal to 230 GΩ; Vm equal to -100 mV; scale bar 2 pA/100 ms. Additional analyses revealed unchanged single-channel chord conductance, voltage dependence, and open/closed dwell-time distributions (not shown). (B) Osmotic lysis of infected cells in sorbitol lysis solution with (red curve) or without (black) 1 mM DTE. Increasing the DTE concentration to 50 mM or adding preincubation with DTE also had no effect; similar results were obtained with the 8 parasite isolates listed in “Results” and in 14C-sorbitol uptake studies (not shown). (C) Osmotic lysis of uninfected RBCs in sorbitol lysis solution after preincubation with (red curve) or without (black curve) 1 mM t-butyl hydroperoxide for 15 minutes with a 2.5-hour postincubation period at 37°C, as in Huber et al.10  Increasing the postincubation period to 24 hours also had no effect (not shown). Although the transmittance values are presented in arbitrary units, their scaling is conserved in panels B and C so that %T equal to 80 corresponds to complete osmotic lysis.

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