Soluble rage protein
AssigneeJapan as Represented by President of Kanazawa University
InventorsHiroshi Yamamoto, Hideto Yonekura, Yasuhiko Yamamoto, Shigeru Sakurai, Takuo Watanabe
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AssigneeJapan as Represented by President of Kanazawa University
InventorsHiroshi Yamamoto, Hideto Yonekura, Yasuhiko Yamamoto, Shigeru Sakurai, Takuo Watanabe
Estimating the term…
The object of this invention is to elucidate the factors involved in the regulation of AGE (advanced glycation endproducts, which are produced in a living body accompanied with diabetes and aging) and RAGE (the receptor for AGE), in order to facilitate investigation on the biological activities, physiological phenomenon and diseases related to AGE and RAGE. Plural molecular species are known to exist for RAGE, and among such molecular species, soluble RAGE exhibits the activity to modulate interaction between AGE and transmembrane-type RAGE. Using this soluble RAGE or a nucleic acid encoding it, the soluble RAGE can be measured, in addition, investigation on various physiological phenomenon, biological activities, and diseases related to interaction between AGE and RAGE can be performed to facilitate development a medicine having further efficacy.
(Canceled)
A nucleic acid having a base sequence coding for the polypeptide according to claim 23.
A primer available for PCR amplification of the open reading frame region of the base sequence as described in the SEQ ID No. 1 of the sequence listing, a partial sequence thereof, or a base sequence substantially equivalent to the open reading frame region.
A pharmaceutical composition containing a compound capable of promoting or inhibiting biological activity of the polypeptide according to claim 23 or a salt thereof, or the nucleic acid according to claim 3.
A method for screening or a screening kit useful for carrying out the method, for screening a compound capable of promoting or inhibiting the biological activity of the polypeptide according to claim 23 or a salt thereof, or the nucleic acid according to claim 3 using any one selected from the group consisting of the polypeptide according to claim 23 or a salt thereof, the nucleic acid according to claim 3 or the vector according to claim 5.
A chimera molecular compound obtained by conjugating the polypeptide according to claim 23 with an amino acid sequence derived from a organism of different species.
A genetic diagnosis agent for diagnosing diseases related to the soluble RAGE polypeptide, which is for detection of presence of a mutated region existing in the soluble RAGE polypeptide, or in the gene or RNA coding for the soluble RAGE, wherein the mutated region is capable of altering expression or activity of the soluble RAGE poltypeptide.
A method for genetic diagnosis for diseases related to the soluble RAGE gene comprising the steps of:
A polypeptide described in any one of the following (1) to (4) or a salt thereof:
Dependencies are inferred from the claim text.