IP Library Granted Patent US 9,873,879
Granted Patent B2
US 9,873,879 · App. 15/359,879 · Granted Jan 23, 2018

Nucleic acid fragment binding to target protein

Inventors: Ichiro Hirao (Tokyo, JP); Michiko Hirao (Tokyo, JP); Rie Yamashige (Saitama, JP); Shigeyuki Yokoyama (Saitama, JP)
Assignee: Tagcyx Biotechnologies
C12N15/115A61K48/00C12N15/1048C12N15/111C12N15/113C12Q1/6869G01N33/5308C12N2310/12C12N2310/16C12N2310/33C12N2310/331C12N2320/13
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Quick Facts
Patent No.
US 9,873,879
App. No.
15/359,879
Granted
Jan 23, 2018
Kind
B2
Abstract

An object of the present invention is to develop and provide a method for efficiently producing a nucleic acid aptamer, particularly, a DNA aptamer, having higher specificity and binding activity against a target substance than those of nucleic acid aptamers obtained by conventional methods. The present invention provides a transcribable or replicable nucleic acid aptamer comprising a natural nucleotide and a non-natural nucleotide having an artificial base-pairable artificial base. The present invention also provides a method for sequencing a non-natural nucleotide-containing single-stranded nucleic acid molecule selected from a single-stranded nucleic acid library.

Claims (16)

1. A transcribable or replicable nucleic acid aptamer comprising:

natural nucleotides and

non-natural nucleotides having an artificial base-pairable artificial base,

wherein the artificial base is selected from the group consisting of 7-(2-thienyl)-3H-imidazo [4 5-b] pyridin-3-yl 2-nitropyrrol-1-yl, and 2-formyl-1H-pyrrol-1-yl, and

wherein the nucleic acid aptamer is directed against a vascular endothelial growth factor as a target substance,

wherein the nucleic acid aptamer comprises any one nucleotide sequence selected from the group consisting of SEQ ID NOs: 25 to 73, 80 to 104, 106 to 109, 111, and 115 to 166 (provided that “n” in the sequences represents 7-(2-thienyl)-3H-imidazo[4,5-b]pyridin-3-y]), 175, 177, 179, 181, 183, 198, 201, 202, 205 to 209, 211, 212, and 229 to 278.

2. The nucleic acid aptamer according to claim 1 ,

wherein the artificial base includes an artificial base-pairable derivative of the artificial base.

3. The nucleic acid aptamer according to claim 1 ,

wherein the content of the non-natural nucleotide is 20% or less of the total number of nucleotides.

4. The nucleic acid aptamer according to claim 1 ,

wherein the nucleic acid is a DNA or an RNA.

5. The nucleic acid aptamer according to claim 1 ,

wherein the nucleic acid aptamer consists of any one nucleotide sequence according to claim 1 that is 5′ flanked by the nucleotide sequence represented by SEQ ID NO: 1 and 3′ flanked by the nucleotide sequence represented by SEQ ID NO: 2.

6. A pharmaceutical composition which comprises a nucleic acid aptamer according to claim 1 as an active ingredient and functionally inhibits a target substance of the nucleic acid aptamer.

7. A pharmaceutical composition for functional inhibition of a vascular endothelial growth factor, comprising a nucleic acid aptamer according to claim 1 as an active ingredient.

Assignments (1)
CHANGE OF ASSIGNEE ADDRESS Recorded Feb 28, 2018
From: TAGCYX BIOTECHNOLOGIES
To: TAGCYX BIOTECHNOLOGIES
Reel/Frame 045472/0250 →
Priority Claims (2)
JP 2011-253357 · Nov 18, 2011 · national
JP 2012-148962 · Jul 2, 2012 · national
Continuity (2)
Division 14358895
Related Publication 20170073683A1 · Mar 16, 2017