Therapeutic use of the SMR1 protein and active derivatives...

Chemistry: molecular biology and microbiology – Measuring or testing process involving enzymes or...

Reexamination Certificate

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C435S007800, C436S063000, C436S503000, C436S815000

Reexamination Certificate

active

07429448

ABSTRACT:
The present invention pertains to the use of a peptide molecule consisting in a maturation product of SMR1 (Submandibular rat protein 1) of structural formula QHNPR, as well as the biologically active derivatives of the said peptide, for preventing or treating diseases associated with a mineral ion imbalance in a human or an animal body. More particularly, the present invention relates to the therapeutic use of the above-cited molecules for preventing or treating an hydro-mineral imbalance in organs and tissues such as kidney, bone, dental enamel, dental ivory, gut matrix, pancreas or glandular gastric mucosa. This invention also deals with therapeutic compositions comprising a pharmaceutically active amount of the above-described therapeutic molecules as well as with therapeutic methods using the said therapeutic compositions. Finally, the present invention relates to processes for selecting ligand molecules that possess an agonist or an antagonist biological activity on the target receptor of the QHNPR pentapeptide as well as to the selected ligand molecules themselves.

REFERENCES:
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patent: 6589750 (2003-07-01), Rougeot et al.
patent: 0 240 975 (1987-10-01), None
patent: WO 90/03981 (1990-04-01), None
patent: WO 95/00848 (1995-01-01), None
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Rougeot et al., “Targets for SMR1-Pentapeptide Suggest a Link Between the Circulating Peptide and Mineral Transport,” Am. J. Physiology, vol. 273, No. 4 PT2, Oct. 1997, pp. R1309-1320.
Singer et al., “Recent evolution of genes encoding the prohormone-like protein SMR1 in the rat submandibular gland,” DNA Cell Biology, vol. 14, No. 2, 1995, pp. 137-144.
Courty et al., “Episodic evolution and rapid divergence of members of the rat multigene family encoding the salivary prohormone-like protein SMR1,” Molecular Biology and Evolution, vol. 12, No. 6, 1996, pp. 758-766.
Drews R et al., “Proteolytic Maturation of Protein C Upon Engineering the Mouse Mammary Gland to Express Furin,” Proceedings of the National Academy of Sciences of USA, vol. 92, No. 23, Nov. 1995, pp. 10462-10466.
Drucker et al., “Regulation of the biological activity of glucagon-like peptide 2 in vivo by dipeptidyl peptidase,” Nature Biotechnology, (Abstract), 1997.
U.S. Appl. No. 11/594,105, filed Nov. 08, 2006, Rougeot, et al.
U.S. Appl. No. 10/620,462, filed Jul. 17, 2003, Rougeot, et al.

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