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Fig. 1. Differential binding of Shiga anCd cholera toxin to Vero cells; differences
in gene expression in Shiga versus Cholera toxin binding Vero cells. (a)
Differential binding of Cy3-CTX (CTX-Cy3) and Cy2-ST (ST-Cy2) to
non-synchronized Vero cells. Cells were incubated simultaneously with the two
labeled toxins for 10 minutes at 0°C. Unbound toxins were washed away and
the live cells observed by fluorescence microscopy. (b) Differential display
comparing ST binding cells (S) and CTX binding cells (C). Non-synchonized Vero
cells were labeled simultaneously with Cy2-ST and Cy3-CTX as in (a) and
separated by FACS. cDNA was synthesized from RNA extracted from ST and CT
binding cells. DNA fragments were produced by PCR using different 5' and
3' primers and analyzed by PAGE. The results of the primer pairs P2/T1,
P2/T2, P2/T3, and P2/T4 are shown (see Methods section). Note the
differentially amplified cDNA fragments marked by (*).