Human DNase II

Details Human DNase II Human DNase II

2001-05-18

2003-05-27

Saidha, Tekchand (Department: 1652)

Drug, bio-affecting and body treating compositions

Enzyme or coenzyme containing

Hydrolases

C435S196000, C435S199000, C435S252300, C435S320100, C536S023200

Reexamination Certificate

active

06569429

ABSTRACT:

FIELD OF THE INVENTION
The present invention relates to newly identified human deoxyribonuclease (DNase) protein, nucleic acid encoding such protein, the use of such protein and nucleic acid, as well as the production of such protein and nucleic acid, for example, by recombinant DNA methods.
BACKGROUND OF THE INVENTION
Deoxyribonuclease (DNase) is a phosphodiesterase capable of hydrolyzing polydeoxyribonucleic acid, and is known to occur in several molecular forms. Based on their biochemical properties and enzymatic activities, DNase proteins have been classified as two types, DNase I and DNase II. DNase I proteins have a pH optimum near neutrality, an obligatory requirement for divalent cations, and produce 5′-phosphate nucleotides on hydrolysis of DNA. DNase II proteins exhibit an acid pH optimum, do not require divalent cations for activity, and produce 3′-phosphate nucleotides on hydrolysis of DNA.
DNase from various species have been purified to a varying degree. For example, various forms of bovine DNase I have been purified and completely sequenced (Liao, et al., J. Biol. Chem. 248:1489-1495 (1973); Oefner, et al., J. Mol. Biol. 192:605-632 (1986); Lahm, et al., J. Mol. Biol. 221:645-667 (1991)), and DNA encoding bovine DNase I has been cloned and expressed (Worrall, et al., J. Biol. Chem 265:21889-21895 (1990)). Porcine and orcine DNase I proteins also have been purified and completely sequenced (Paudel, et al., J. Biol. Chem. 261:16006-16011 (1986); Paudel, et al., J. Biol. Chem. 261:16012-16017 (1986)).
DNA encoding a human DNase I has been isolated and sequenced and the DNA has been expressed in recombinant host cells, thereby enabling the production of human DNase I in commercially useful quantities. Shak, et al., Proc. Natl. Acad. Sci. 87:9188-9192 (1990). The term “human DNase I” will be used hereafter to refer to the mature polypeptide disclosed in Shak, et al.
DNA encoding other polypeptides having homology to human DNase I also have been identified. Rosen, et al., PCT Patent Publication No. WO 95/30428, published Nov. 16, 1995; Parrish, et al., Hum. Mol. Genet. 4:1557-1564 (1995); Baker, et. al., U.S. patent application Ser. No. 08/597,078 (filed Feb. 5, 1996).
DNase I has a number of known utilities and has been used for therapeutic purposes. Its principal therapeutic use has been to reduce the viscoelasticity of pulmonary secretions (including mucus) in such diseases as pneumonia and cystic fibrosis (CF), thereby aiding in the clearing of respiratory airways. See e.g., Lourenco, et al., Arch. Intern. Med. 142:2299-2308 (1982); Shak, et al., Proc. Natl. Acad. Sci. 87:9188-9192 (1990); Hubbard, et al., New Engl. J. Med. 326:812-815 (1992); Fuchs, et al., New Engl. J. Med. 331:637-642 (1994); Bryson, et al., Drugs 48:894-906 (1994). Mucus also contributes to the morbidity of chronic bronchitis, asthmatic bronchitis, bronchiectasis, emphysema, acute and chronic sinusitis, and even the common cold. DNase I is effective in reducing the viscoelasticity of pulmonary secretions by hydrolyzing, or degrading, high-molecular-weight DNA that is present in such secretions. Shak, et al., Proc. Natl. Acad. Sci. 87:9188-9192 (1990); Aitken, et al., J. Am. Med. Assoc. 267:1947-1951 (1992).
Various forms of DNase II also have reportedly been purified, including bovine DNase II (Lesca, J. Biol. Chem. 251:116-123 (1976)), human DNase II (Yamanaku, et al., J. Biol. Chem. 249:3884-3889 (1974); Murai, et al., J. Biochem. 87:1097-1103 (1980); Harosh, et al., Eur. J. Biochem. 202:479-484 (1991); Yasuda, et al., Biochem. Biophys. Acta 1119:185-193 (1992)), porcine DNase II (Bernardi, et al., Biochemistry 4:1725-1729 (1965); Liao, et al., J. Biol. Chem. 260:10708-10713 (1990)), and rat DNase II (Dulaney, et al., J. Biol. Chem. 247:1424-1432 (1972)). The physical properties of the human DNase II proteins described in these reports vary considerably (e.g., reported molecular weights range from 32,000 to 45,000 Daltons), which leads to uncertainty whether there is one or multiple naturally occurring forms of the human protein.
Recent interest in human DNase II has arisen because of its possible role in the programmed cell death process of apoptosis (Barry, et al., Arch. Biochem. Biophys. 300:440-450 (1993); Barry, et al., Cancer Res. 53:2349-2357 (1993)). One of the events that is characteristic of that process is the degradation of nuclear DNA into nucleosomal fragments. The ability to prevent or inhibit the expression of human DNase II or its enzymatic activity within human cells may be important in preventing or limiting such intracellular destruction of DNA, and thus may be an effective means of interrupting the process of apoptosis. In other instances, it may be useful to increase the expression of human DNase II within a certain population of cells within a human patient, such as cancer cells, in order to induce apoptosis of those cells.
SUMMARY OF THE INVENTION
The present invention provides human DNase II protein, as well as analogs and variants thereof, that have DNA-hydrolytic activity. As is characteristic of DNase II proteins in general, the human DNase II of the present invention exhibits an acid pH optimum, and does not require divalent cation for activity.
The invention also provides nucleic acids encoding human DNase II, recombinant vectors comprising such nucleic acids, recombinant host cells transformed with those nucleic acids or vectors, and processes for producing human DNase II by means of recombinant DNA technology. The invention includes the use of such nucleic acids and vectors for in vivo or ex vivo gene therapy.
The invention also provides complementary nucleic acids, including so-called anti-sense oligonucleotides, that are capable of binding to and preventing the expression of nucleic acid within a cell that encodes human DNase II.
The invention also provides pharmaceutical compositions comprising human DNase II, optionally together with a pharmaceutically acceptable excipient, as well as substantially purified antibodies that are capable of binding to human DNase II.
The invention also provides methods for reducing the viscoelasticity or viscous consistency of DNA-containing material in a patient, comprising administering a therapeutically effective dose of human DNase II to the patient. The invention is particularly directed to a method of treating a patient having a disease such as cystic fibrosis, chronic bronchitis, pneumonia, bronchiectasis, emphysema, asthma, or systemic lupus erythematosus, that comprises administering a therapeutically effective amount of human DNase II to the patient. The invention also is directed to the use of human DNase II in vitro, such as for degrading DNA that is present in a biological specimen or other material, and in diagnostic and other assays.
These and other aspects of the invention will be apparent to the ordinary skilled artisan upon consideration of the following detailed description.


REFERENCES:
Harosh et al., “Mechanism of action of deoxyribonuclease II from human lymphoblasts”European Journal of Biochemistry202:479-484 (1991).
Murai et al., “Purification and Properties of Deoxyribonuclease II from Human Urine”J. Biochem. 87:1097-1103 (1980).
Sambrook et al.Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Lab Press pps. 11.3-11.19 (1989).

Affiliated with

Also associated with

Rating

Human DNase II does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with Human DNase II, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Human DNase II will most certainly appreciate the feedback.

Rate now

Comments { 0 }

Profile ID: LFUS-PAI-O-3043038