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. 2010 May 13;9(7):1554–1566. doi: 10.1074/mcp.M000022-MCP201

Fig. 4.

Fig. 4.

Analyses of six parasite strains for adherence and biotinylation. A, binding to ectocervical cells. Parasites from six different strains were fluorescently labeled and incubated with ectocervical cell monolayers at 37 °C. Coverslips were washed to remove non-adherent parasites, mounted, and visualized and quantified by fluorescence microscopy. Data are expressed as percentage of adhesion related to the PA strain ± the standard deviation of the mean. A representative experiment of three independent experiments is shown. B, surface protein biotinylation of strains with different adherence capacities. A comparable amount of protein extract of three less adherent (T1, G3, and SD10) and three highly adherent strains (PA, B7268, and SD7) was loaded onto a streptavidin column (left panel). Biotinylated labeled proteins were recovered, separated by SDS-PAGE, and silver-stained (middle panel) or detected by Western blot (WB) with an anti-biotin antibody (right panel). The molecular weight marker is shown on the far left.