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. 2011 Mar 2;100(5):1325–1334. doi: 10.1016/j.bpj.2011.01.037

Figure 7.

Figure 7

Anionic supramolecular assemblies have a limited capacity to inhibit SEVI-mediated enhancement of HIV-1 infection. (A) SEVI fibrils (5 μM) were allowed to form a complex with HIV-1 virions for 10 min at room temperature. The anionic peptide supramolecular assemblies were then added to the SEVI:virus solution and incubated for 10 min. This solution was then incubated on CEMx M7 cells. After 48 h, the cells were harvested and luciferase expression measured as a readout of HIV-1 infection. (B) HIV-1 infections were performed on CEMx M7 cells in the presence of increasing concentrations of E4(ChaKChaE)2 alone, in the absence of SEVI. Results in both panels represent mean values from three experimental replicates; error bars denote the standard deviation of these values. The results shown are representative of three independent experiments performed with a range of anionic peptide concentrations all yielding similar results.