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. 2017 Jan 18;91(3):e01880-16. doi: 10.1128/JVI.01880-16

TABLE 4.

Activation of fusion between Env-expressing cells and CD4-negative, CCR5-positive cells

Compound Incubation time (min) Area under the curve (arbitrary units) for HIV-1 Enva:
AD8 JR-FL JR-FL Y177R JR-FL P183Y
NBD-556 5 <10 <10 36 <10
10 <10 <10 23 <10
30 <10 <10 106 <10
60 <10 <10 105 <10
JRC-II-191 5 <10 <10 140 <10
10 <10 <10 272 <10
30 <10 <10 411 <10
60 <10 <14 285 <10
DMJ-II-121 5 47 161 1,139 354
10 94 171 659 335
30 32 19 679 146
60 <10 <10 168 12
JP-III-48 5 59 59 877 12
10 69 12 884 29
30 25 30 1,175 19
60 20 29 746 15
BNM-III-170 5 47 74 1,567 76
10 37 77 1,095 90
30 66 27 1,334 58
60 14 27 872 60
a

Different concentrations (0 to 100 μM) of the CD4mc were incubated with 293T cells expressing HIV-1 Env variants and the α peptide of β-galactosidase at 37°C for the indicated times. The cells were then washed and cocultivated with CD4-negative CCR5-positive Cf2Th-CCR5 cells expressing the ω peptide of β-galactosidase at 37°C in medium without the CD4mc. After 6 h, the extent of cell-cell fusion was assessed by measuring β-galactosidase activity in the cell lysates. The β-galactosidase activity was plotted as a function of the CD4mc concentration, and the area under the curve was measured for each time point. The results of a typical experiment out of two independent experiments are shown.