1. Partial characterization of a human submandibular/sublingual salivary adhesion-promoting protein.
- Author
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Akintoye SO, Dasso M, Hay DI, Ganeshkumar N, and Spielman AI
- Subjects
- Blotting, Western, Chromatography, Gel, Dental Caries microbiology, Durapatite, Electrophoresis, Polyacrylamide Gel, Humans, Immunohistochemistry, Molecular Weight, Salivary Proteins and Peptides isolation & purification, Streptococcus mutans physiology, Submandibular Gland metabolism, Bacterial Adhesion, Salivary Proteins and Peptides chemistry
- Abstract
Human submandibular/sublingual saliva contains a protein that promotes adhesion of Streptococcus mutans JBP serotype-c to spheroidal hydroxyapatite in vitro. A high molecular-weight (250,000-300,000 Da) adhesion-promoting protein (APP) was purified by Trisacryl 2000 M gel-filtration chromatography and gel electroelution before it was partially characterized. Lectin blotting identified that the terminal carbohydrates include N-acetyl glucosamine-beta 1-4-N-acetylglucosamine, galactose and galactose-beta 1-3-N-acetyl galactosamine. Antibodies to APP demonstrated no difference in the immunoreactive pattern of APP from saliva of caries-active or caries-resistant individuals belonging to four different ethnic groups: Asian, African-American, Hispanic or Caucasian. No immunological similarities to salivary mucins or parotid agglutinins were detected by Western blotting using immuno-cross-reactivity as a criterion. APP appears to be a unique protein found in submandibular/sublingual saliva. Understanding such a protein could help prevent S. mutans attachment to the enamel surface.
- Published
- 2002
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