Figure 1
Figure 1. Atomic force microscopy (AFM) setup. (A) AFM schematic. (B) Functionalization of AFM. Molecules depicted represent a composite of 2 sets adsorbed or captured on the AFM tip or the polystyrene dish. A1A2A3 tridomain was directly adsorbed or captured by anti-His mAb preadsorbed on the surface. GPIbα or CR1 was adsorbed on the cantilever tip. (C) Binding specificity. Immobilized A1A2A3 bound GPIbα- or CR1-coated cantilever tips but not BSA-coated tips. ND indicates not done. GPIbα did not bind captured A1A2A3 probably because of its different conformation from adsorbed A1A2A3.

Atomic force microscopy (AFM) setup. (A) AFM schematic. (B) Functionalization of AFM. Molecules depicted represent a composite of 2 sets adsorbed or captured on the AFM tip or the polystyrene dish. A1A2A3 tridomain was directly adsorbed or captured by anti-His mAb preadsorbed on the surface. GPIbα or CR1 was adsorbed on the cantilever tip. (C) Binding specificity. Immobilized A1A2A3 bound GPIbα- or CR1-coated cantilever tips but not BSA-coated tips. ND indicates not done. GPIbα did not bind captured A1A2A3 probably because of its different conformation from adsorbed A1A2A3.

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