TEXT

Top Abstract Text References

Periodontal diseases are infectious in nature and induce an inflammatory response in the gingival and underlying supportive periodontal tissues in response to bacterial accumulation in the subgingival crevice. Porphyromonas gingivalis, a gram-negative black-pigmented anaerobe, has been strongly implicated as an etiologic agent of periodontitis in adults (16). The organism has been shown to produce a variety of virulence factors in both cell-associated and cell-free forms. Among them, fimbriae, fine fibrillar proteinaceous appendages emerging from the cell surface, are thought to be critical factors in the adherence of the organism to the gingival margin (4). Purified fimbriae have been reported to bind to epithelial cells, fibroblasts, human salivary components, collagen, and fibronectin (1, 4, 11-13). We previously purified an arginine-specific cysteine protease (RC-protease) from P. gingivalis 381. The purified enzyme was found to enhance fimbrial binding to fibroblasts or extracellular matrix (ECM) proteins. The protease exposed a cryptic receptor on the host matrix proteins, (X)_n-Arg-COOH, and this site increased fimbrial binding to the host proteins. We have simultaneously found that addition of L-Arg, or oligopeptides containing Arg residues at the C terminus, clearly inhibit fimbrial binding to cryptic receptors (11, 12). In this regard, it should be noted that RC-protease appears to be very similar to Arg-gingipain, encoded by rgpB, as reported by Nakayama et al. (15), in terms of molecular size, amino-terminal sequence, and some enzymatic properties. Thus, these findings suggest that RC-protease of P. gingivalis plays an important role in adherence of the organism to host tissue.

The rationale of this study was to seek natural peptides rich in the Arg residue to obtain good inhibition of P. gingivalis RC-protease. Should such agents be found and used on a wide scale, elimination or reduction in the numbers of P. gingivalis organisms from the oral cavity would eventually be possible.

Protamines are found in fish spermatozoan nuclei in large quantities, where their presence appears to compact DNA. Protamines are highly basic peptides (pI > 10) due to a high arginine content (21 arginines out of 32 amino acids) (2). In our survey of RC-protease inhibitors from natural resources, we found that protamines exhibited a marked inhibitory effect on protease activity. Therefore, we examined the inhibitory mechanisms of protamines for the proteolytic activity of RC-protease and the interaction of fimbriae with immobilized fibronectin treated with RC-protease.

Inhibitory effect of protamines on the protease activity of P. gingivalis. RC-protease was extracted from cell paste by sonication in phosphate buffer containing 0.2% Triton X-100 and was purified by column chromatography, as described previously (12). The proteolytic activity of the purified RC-protease (7 U/ml; specific activity, 54 U/mg) was determined with benzoyl-L-arginine 4-methyl-coumary-7-amide, as described previously (12). Inhibitory effects of various reagents on proteolytic activity were measured by using a 300 µM concentration of a synthetic chromogenic substrate, benzoyl-L-arginine-p-nitroanilide (Bz-L-Arg-pNA) (Peptide Inst., Minoo-Osaka, Japan), in 12.5 mM sodium phosphate buffer (pH 7.5) containing 375 µM CaCl₂ and 560 µM cysteine (1-ml final volume). After an appropriate incubation period at 37°C, the amount of released p-nitroanilide (pNA) was colorimetrically read at A₄₀₅. Among various protamines, salmin (composed of 32 amino acid residues: PRRRRSSSRPVRRRRRPRVSRRRRRRGGRRRR) from salmon and clupeine (31 residues: ARRRRSSSRPIRRRRPRRRTTRRRRAGRRRR) from herring were obtained from Sigma Chemical Co. (St. Louis, Mo.). They were dissolved in distilled water and used immediately after filtration (pore size, 0.2 µm). Chymostatin, a chymotrypsin inhibitor, and pepstatin, an aspartic-proteinase inhibitor, were purchased from Peptide Inst. and used as control enzyme inhibitors. As shown in Fig. 1, protamines were found to markedly inhibit the proteolytic activity of RC-protease, and a 50% inhibitory effect was observed at a 60 µM concentration of each protamine. The inhibitory levels were significantly higher than those of pepstatin when 30 µM concentrations of protamines or pepstatin were used.

View larger version (29K): [in this window] [in a new window]   FIG. 1.   Inhibitory effect of protamines (salmine or clupeine) against P. gingivalis RC-protease. Proteolytic activity was measured by using the synthetic chromogenic substrate Bz-L-Arg-pNA (300 µM) in 12.5 mM sodium phosphate buffer (pH 7.5) containing 375 µM CaCl2, 560 µM cysteine, and protamines (0 to 1,000 µg/ml). After an appropriate incubation period at 37°C, the amount of released pNA was read colorimetrically at 405 nm. Values are presented as means ± standard deviations of triplicate assays performed on three separate occasions.

View larger version (121K): [in this window] [in a new window]   FIG. 2.   SDS-PAGE profile of collagen and fibronectin with or without pretreatment of P. gingivalis RC-protease. Protein specimens were incubated at 37°C for 1 h in the presence or absence of RC-protease, and the protein profile of each reaction mixture was determined by SDS-PAGE followed by staining with Coomassie brilliant blue. Lanes A, reaction mixture in the absence of RC-protease and protamines; lanes B, reaction mixture in the presence of RC-protease (1 mU/ml) and in the absence of protamines; lanes C, reaction mixture in the presence of RC-protease (1 mU/ml) and salmine (100 µg/ml); lanes D, reaction mixture in the presence of RC-protease (1 mU/ml) and clupeine (100 µg/ml).

Fimbrial binding to immobilized protamines or fibronectin. Fimbriae were prepared from P. gingivalis 381 cells, as described previously (11). The purified fimbriae (10 mg) were biotinylated by incubation with 1.2 mg of biotin-N-hydroxysuccinimide (Calbiochem, La Jolla, Calif.) in 11 ml of 100 mM NaH₂CO₃ (pH 8.0) at 25°C for 2 h, followed by dialysis against phosphate-buffered saline, pH 7.4 (PBS). Various concentrations of protamines (100 µl of 0 to 100 µg/ml in PBS) were added to microtiter wells (Maxisorp; Nalge Nunc International) and left overnight at 4°C for immobilization. After being washed with PBS three times, biotinylated fimbriae (0.7 µg/100 µl) were added to the wells and incubated for 0.5 h. The amount of bound fimbriae was colorimetrically determined after washing of the wells with PBS. As shown in Fig. 3, fimbriae were found to clearly bind to the immobilized salmine and clupeine. The amount of fimbrial binding increased as the concentrations of protamines used for immobilization increased. Fimbrial binding to bovine serum albumin was negligible.

View larger version (23K): [in this window] [in a new window]   FIG. 3.   Binding of biotinylated fimbriae to immobilized protamines. After immobilization of salmine or clupeine to wells, biotinylated fimbriae (0.7 µg) were added to the wells and incubated. The amount of fimbriae bound was colorimetrically determined by using streptavidin-alkaline phosphatase. Values are means ± standard deviations (SD) of triplicate assays performed on three separate occasions. SD were within ±5% of the means.

View larger version (55K): [in this window] [in a new window]   FIG. 4.   Inhibitory effect of salmine and clupeine on binding of fimbriae to immobilized fibronectin with treatment of P. gingivalis RC-protease. After immobilization of fibronectin to wells, biotinylated fimbriae (0.7 µg) were added with the protease (7 mU/ml) and salmine or clupeine (0 to 300 µg/ml) to the wells. The amount of bound fimbriae was colorimetrically determined by using streptavidin-alkaline phosphatase. Results are expressed relative to the fimbrial binding of the control (without RC-protease treatment or protamines). Values are means ± standard deviations of triplicate assays performed on three separate occasions.

Kinetic analyses of the inhibitory effect of protamines on RC-protease. Kinetic analyses were then carried out to demonstrate the mechanism of inhibition of protamines against RC-protease. Briefly, Bz-L-Arg-pNA was added at final concentrations of 2, 4, and 8 µM to the assay mixture composed of 12.5 mM sodium phosphate buffer containing 375 µM CaCl₂ and 560 µM cysteine, pH 7.5, with or without protamines. After incubation at 37°C for 5 min, the reaction was started by the addition of RC-protease (7 mU) to the mixture (1-ml final volume). The amount of released pNA was determined by the change of absorbance at 405 nm. The K_m value was determined to be 2.8 µM (Fig. 5A and C), while the K_i values were determined from Lineweaver-Burk plots to be 0.2 to 0.4 µM (Fig. 5B and D). These results showed that protamines were competitive inhibitors to the substrate, Bz-L-Arg-pNA.

View larger version (55K): [in this window] [in a new window]   FIG. 5.   Kinetic analyses of the inhibitory effects of protamines on RC-protease. Bz-L-Arg-pNA (2, 4, and 8 µM final concentrations) was added to the assay mixture composed of 12.5 mM sodium phosphate buffer (pH 7.5), 375 µM CaCl2, and 560 µM cysteine with or without protamines. After incubation at 37°C for 5 min, the reaction was started by the addition of RC-protease (7-mU/ml final concentration). The amount of released pNA was read by the change in absorbance at 405 nm. All assays were done in triplicate, and mean values were used for determination of Km and Ki values.