Polyclonal antihuman CY -thrombin antibodies produced in rabbits reacted minimally (<0.05%) in solution with human prothrombin. However, when prothrombin was adsorbed to artificial surfaces such as polyvinyl chloride (PVC), the crossreactivity of surface-bound prothrombin with antibody IgG to thromb
Local Conformational Changes of Vitronectin upon Adsorption on Glass and Silane Surfaces
โ Scribed by Filip Banovac; Steven S. Saavedra; George A. Truskey
- Publisher
- Elsevier Science
- Year
- 1994
- Tongue
- English
- Weight
- 593 KB
- Volume
- 165
- Category
- Article
- ISSN
- 0021-9797
No coin nor oath required. For personal study only.
โฆ Synopsis
The conformation of vitronectin ((\mathrm{Vn})) in solution and adsorbed to hydrophilic and hydrophobic glass was studied using the polarity-sensitive fluor acrylodan. Free sulfhydryl groups of vitronectin were labeled with acrylodan under nondenaturing conditions. The number and location of the free sulfhydryl groups were determined by cleavage with either formic acid or cyanogen bromide followed by polyacrylamide gel electrophoresis. Based upon published amino acid sequences of (\mathrm{Vn}), the fluorescence of acrylodan-labeled (\mathrm{Vn}(\mathrm{Ac}-\mathrm{Vn})) fragments is consistent with free sulfhydryls being located at cysteine residues 196 and 274. Conformational changes upon adsorption on glass and silanized glass surfaces placed the free sulfhydryl residues in a more hydrophobic environment than was observed when Vn was in PBS solution. Small but statistically significant quenching of (\mathrm{Ac}-\mathrm{Vn}) fluorescence with iodide could be explained in terms of a twosite model. Results of this study suggest that the domains surrounding the free sulfhydryl groups of vitronectin experience different environments in solution and adsorbed to surfaces.
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