Overexpression of the P185
HER2 protein determines the malignancy and unfavorable prognosis of ovarian and breast tumors. In this work, the distribution of P185
HER2 in human cancer cells was studied by electron microscopy, using a novel approach. It is based on the interaction between barnase (a ribonuclease from
Bacillus amyloliquefaciens) and its specific inhibitor barstar. The monoclonal antibody 4
D5 scFv to extracellular P185
HER2 domain fused with two molecules of barnase was used as a recognizing agent, and the conjugate of colloidal gold with barstar, as an electron dense label for electron microscopic visualization. For labeling, we used supramolecular complexes 4D5 scFv-dibarnase:barstar-Au.
The distribution of P185HER2 in human ovarian carcinoma cells SKOV-3 and breast carcinoma cells BT-474 was studied at 4聽掳C and 37聽掳C. It was shown that at 4聽掳C the protein P185HER2 occurs exclusively on the cell surface, mainly on protrusions or close to their bases. At 37聽掳C, the internalization of P185HER2 caused by its interaction with 4D5 scFv-dibarnase was observed. Inside the cells, P185HER2 was located in the coated pits and vesicles, endosomes and multivesicular bodies.
The data obtained indicate that the supramolecular 4D5 scFv-dibarnase:barstar-gold complex can be used as a new immunodetection system for exploring the P185HER2 distribution.