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Resolution: standard / high Figure 2.
Loss of an N-linked glycan at position 386 in primary HIV Envs enhances macrophage
tropism and neutralization sensitivity to mAb b12. (A) MDM were infected with luciferase-expressing reporter viruses expressing wild-type
or N386D mutant Envs. Cells were lysed 6 days post-infection and analyzed for luciferase
activity. (B, C, D) Luciferase-expressing reporter viruses expressing wild-type or
N386D mutant Envs were incubated with a range of concentrations of human mAb b12 (B),
sCD4 (C), or a HIV-1 neutralizing patient serum (PS; D) 1 h prior to infection of
Cf2 cells transiently expressing CD4 and CCR5. Cells were harvested 48 h post infection
and assayed for luciferase activity. Data are expressed as the concentrations at which
luciferase expression was reduced by 50% compared to infection in the absence of mAb
(IC50). Error bars represent standard deviations.
Dunfee et al. Retrovirology 2009 6:69 doi:10.1186/1742-4690-6-69 |