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. 2014 Oct 13;207(1):159. doi: 10.1083/jcb.20140505109252014c

Casp8p41 generated by HIV protease kills CD4 T cells through direct Bak activation

Amy M Sainski, Haiming Dai, Sekar Natesampillai, Yuan-Ping Pang, Gary D Bren, Nathan W Cummins, Cristina Correia, X Wei Meng, James E Tarara, Marina Ramirez-Alvarado, David J Katzmann, Christina Ochsenbauer, John C Kappes, Scott H Kaufmann, Andrew D Badley
PMCID: PMC4195834

Vol. 206 No. 7, September 29, 2014. Pages 867–876.

Due to an error during the production process, an incorrect version of Fig. 3 was published. Specifically, incorrect images were included for the top two panels of part I, and several figure parts contained minor formatting and labeling errors. A corrected version of the figure is shown below.

Figure 3.

Figure 3.

Casp8p41 facilitates Bak oligomerization and Bak-mediated MOMP. (A) Dextran-FITC–loaded liposomes composed of MOM lipids were incubated with 50 nM His6-BakΔTM in the absence or presence of 200 nM GST, GST-Casp8p41, or GST-Casp8p41 V150E/L157K at 37°C for 30 min. Bim BH3 peptide served as a positive control. After bismaleimidohexane cross-linking, samples were subjected to SDS-PAGE and blotted for Bak. (B) After His6-BakΔTM was incubated with GST or GST-Casp8p41 in buffer containing 1% (wt/vol) CHAPS, fractions from size exclusion chromatography were blotted for Bak and GST. Representative of n = 3. (C) FITC-dextran release over time from FITC-dextran–loaded liposomes treated as in A. Representative of n = 3. (D) Summarized results from three independent experiments at 300 s of FITC-dextran release from liposomes. (E) FITC-dextran release from liposomes treated with 50 nM His6-BakΔTM in the presence of 200 nM GST-Casp8p41, GST-Casp8p41 V150E/L157K (EK), or GST. 100% release in D and E was determined by treating liposomes with Triton X-100. Error bars indicate ±1 SD from three independent experiments (*, P < 0.05; ***, P < 0.001). (F–J) After mitochondria (F) from wt (G), Bax−/−Bak−/− double knockout (H), Bax−/− (I), or Bak−/− (J) MEFs were incubated with 200 (1), 500 (2), or 1,000 nM (3) of purified protein for 1 h, sedimented, and washed, the supernatants and pellets were blotted for cytochrome c (Cyto C) and, as a control, the mitochondrial matrix protein Hsp60. Bim BH3 (200 nM), which induces CytoC release in the presence of either Bak or Bax, served as a positive control. Representative of n = 3.

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