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. 2013 Mar;87(5):2835–2845. doi: 10.1128/JVI.02209-12

Fig 8.

Fig 8

Quantification of inhibiting activity of HD5 and E21R-HD5 against strain HIVHTLV-IIIB. JLTRG cells (1 × 105) grown in 24-well plates were preincubated with 2-fold serially diluted HD5 or E21R-HD5 peptide (0.3906 to 50 μg/ml) or positive-control peptide C34 (0.00064 to 3.2 μg/ml) for 1 h. H9/HIVHTLV-IIIB cells (1 × 104) were then added to initiate viral infection, and the coculture was maintained for 3 days. Thereafter, the cell samples were analyzed for EGFP expression using flow cytometry. Data presented are means of two independent experiments, with triplicate samples for each point (C34 [a], HD5, and E21R-HD5 [c]). Percent inhibition was calculated by using the formula 100 × [1 − (net percentage of cells EGFP+ × mean fluorescence intensity value of cells EGFP+ in test group)/that in mock group].