Lysine-specific Porphyromonas gingivalis proteinase

Organic compounds -- part of the class 532-570 series – Organic compounds – Carbohydrates or derivatives

Patent

Rate now

  [ 0.00 ] – not rated yet Voters 0   Comments 0

Details

435220, C12N 1551

Patent

active

054750970

ABSTRACT:
Provide herein is a substantially pure Lys-gingipain complex preparation, Lys-gingipain being characterized as having an apparent molecular mass of 105 kDa as estimated by sodium dodecyl sulfate polyacrylamide gel electrophoresis, where sample is prepared without boiling, said Lys-gingipain having amidolytic and proteolytic activity for cleavage after lysine residues and having no amidolytic and/or proteolytic activity for cleavage after arginine residues, wherein the amidolytic and/or proteolytic activity is inhibited by TLCK, cysteine protease group-specific inhibitors including iodoacetamide and iodoacetic acid, wherein the amidolytic and/or proteolytic activity of said Lys-gingipain is not sensitive to inhibition by leupeptin, antipain, trans-epoxysuccinyl-L-leucylamido-(4-guanidino)butane, serine protease group-specific inhibitors including diisopropylfluorophosphate and phenylmethyl sulfonylfluoride, and antibodies specific for the Lys-gingipain protein complex and its catalytic component, methods for preparation. As specifically exemplified, a Lys-gingipain protein complex is purified from Porphyromonas gingivalis H66, and the 60 kDa catalytic component of the Lys-gingipain protein complex has an amino acid sequence as given in SEQ ID NO: 14 from amino acid 1 through amino acid 509. Also provided are nucleic acid sequences encoding this catalytic protein. The nucleotide coding sequence of the 60 kDa catalytic component of the Lys-gingipain protein complex is given in SEQ ID NO:13, from nucleotide 1336 through nucleotide 2863. The Lys-gingipain complex also comprises a hemagglutinin component identified by an N-terminal amino acid sequence as given in SEQ ID NO:14, amino acids 510-714.

REFERENCES:
Lee, C. C., et al. (1988) Science 239, 1288-1291.
Fujimura, S., et al. (1993) FEMS Microbiol. Lett. 113, 133-138.
Pike, R., et al. (1994) J. Bio. Chem. 269 (1), 406-411.
Saggs, J. V., et al. (1981) Proc. Natl. Acad Sci, USA 78(11), 6613-6617.
Young, R. A., et al. (1983) Science 222, 778-782.
U.S. Ser. No. 08/119,361 Sep. 10 1990, Travis et al. filed Sep. 10, 1993.
Scott et al. (1993), "Purification and Characterization of a Potent 70-kDa Thiol Lysyl-proteinase (Lys-gingivain) from Porphyromonas gingivalis That Cleaves Kininogens and Fibrinogen", J. Biol. Chem. 268: 7935-7942.
Travis et al. (1993) "Activation of the Complement and Kinin Pathways by Non-Mammalian Proteinases," Abstract, Kinin 93 Brazil, 21.16.
Chen et al. (1992) "Purification and Characterization of a 50-kDa Cystine Proteinase (Gingipain) from Porphyromonas gingivalis, " J. Biol. Chem. 267: 18896-18901.
Chen et al. (1991) "Stimulation of Proteinase and Amidase Activities in Porphyromonas (Bacteroides) gingivalis by Amino Acids and Dipeptides," Infect. Immun. 59: 2846-2850.
Birkedal-Hansen et al. (1988) "Characterization of Collagenolytic Activity from Strains of Bacteroides gingivalis, " J. Periodontal Res. 23:258-264.
Grenier et al. (1989) "Characterization of Sodium Dodecyl Sulfate-Stable Bacteroides gingivalis Proteases by Polyacrylamide Gel Electrophoresis," Infect. Immun. 57: 95-99.
Ono et al. (1987) "Purification and Characterization of a Thiol-protease from Bacteroides gingivalis Strain 381"; Oral Micr. Immun. 2:77-81.
Madden et al. (1992), "Expression of Porphyromonas gingivalis proteolytic activity in Escherichia coli", Oral Micro. Imm. 7: 349-356.
Uitto V. J. (1987) "Human Gingival Proteases: 1: Extraction and Preliminary Characterization of Trypsin-like and Elastase-like Enzymes"; J. Periodontal Res. 22:58-63.
Sorsa et al. (1987) "A Trypsin-like Protease from Bacteroides gingivalis: Partial Purification and Characterization"; J. Periodont Res. 22:375-380.
Hinode et al. (1992), "Generation of Plasma Kinin by Three Types of Protease Isolated from Porphyromonas Gingivalis 381", Archs oral Biol. 10 (vol. 37) pp. 859-861.
Bourgeau et al. (1992) "Cloning, Expression and Sequencing of a Protease Gene (tpr) from Porphyromonas gingivalis W83 in Escherichia coli", Infect. Immun. 60:3186-3192.

LandOfFree

Say what you really think

Search LandOfFree.com for the USA inventors and patents. Rate them and share your experience with other people.

Rating

Lysine-specific Porphyromonas gingivalis proteinase does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with Lysine-specific Porphyromonas gingivalis proteinase, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Lysine-specific Porphyromonas gingivalis proteinase will most certainly appreciate the feedback.

Rate now

     

Profile ID: LFUS-PAI-O-1360763

  Search
All data on this website is collected from public sources. Our data reflects the most accurate information available at the time of publication.