AFM visualization at a single-molecule level of denaturated states of proteins on graphite

[Display omitted] ⿢High resolution AFM distinguishes conformational states of single adsorbed proteins.⿢Graphite induced protein denaturation is visualized at a single molecule level.⿢Protein denaturation is accompanied by severe morphological changes.⿢GM-HOPG more closely preserves the conformation of adsorbed proteins. Different graphitic materials are either already used or believed to be advantageous in biomedical and biotechnological applications, e.g., as biomaterials or substrates for sensors. Most of these applications or associated important issues, such as biocompatibility, address the problem of adsorption of protein molecules and, in particular the conformational state of the adsorbed protein molecule on graphite. High-resolution AFM demonstrates highly oriented pyrolytic graphite (HOPG) induced denaturation of four proteins of blood plasma, such as ferritin, fibrinogen, human serum albumin (HSA) and immunoglobulin G (IgG), at a single molecule level. Protein denaturation is accompanied by the decrease of the heights of protein globules and spreading of the denatured protein fraction on the surface. In contrast, the modification of HOPG with the amphiphilic oligoglycine-hydrocarbon derivative monolayer preserves the native-like conformation and provides even more mild conditions for the protein adsorption than typically used mica. Protein unfolding on HOPG may have universal character for ⿿soft⿿ globular proteins.