IP Library Granted Patent US 9,725,490
Granted Patent B2
US 9,725,490 · App. 14/235,666 · Granted Aug 8, 2017

ERAP1-derived peptide and use thereof

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Quick Facts
Patent No.
US 9,725,490
App. No.
14/235,666
Granted
Aug 8, 2017
Kind
B2
Abstract

Provided is a novel cancer-treating agent which can be used as a novel choice for the treatment of cancer. Specifically provided are: a peptide that inhibits binding of ERAP1 polypeptide to PHB2 polypeptide, which comprises a binding site of the ERAP1 polypeptide to the PHB2 polypeptide, and a pharmaceutical composition comprising the peptide. In addition, provided is a method for screening a drug candidate for treating and/or preventing cancer using inhibition of the binding of the ERAP1 polypeptide to PP1α polypeptide, PKA polypeptide or PKB polypeptide as an index.

Claims (11)

1. A peptide that inhibits binding of Estrogen Receptor Activity-regulated Protein 1 (ERAP1) polypeptide to prohibitin2 (PHB2) polypeptide, consisting of an amino acid sequence selected from a group consisting of:

an amino acid sequence as set forth in SEQ ID NO: 31;

an amino acid sequence of variant of SEQ ID NO: 31 in which one or two amino acid residues other than glutamine at position 1, aspartic acid at position 5, and glutamine at position 9 of SEQ ID NO: 31 are substituted with other amino acid residues as long as the ability of inhibiting the binding of the ERAP1 polypeptide to the PHB2 polypeptide is maintained;

an amino acid sequence as set forth in SEQ ID NO: 27;

an amino acid sequence of variant of SEQ ID NO: 27 in which one or two amino acid residues other than glutamine at position 1, aspartic acid at position 5 and glutamine at position 9 of SEQ ID NO: 27 are substituted with other amino acid residues as long as the ability of inhibiting the binding of the ERAP1 polypeptide to the PHB2 polypeptide is maintained;

an amino acid sequence as set forth in SEQ ID NO: 30; and

an amino acid sequence of variant of SEQ ID NO: 30 in which one or two amino acid residues other than glutamine at position 5, aspartic acid at position 9 and glutamine at position 13 of SEQ ID NO: 30 are substituted with other amino acid residues as long as the ability of inhibiting the binding of the ERAP1 polypeptide to the PHB2 polypeptide is maintained.

2. The peptide according to claim 1 , wherein the peptide is modified by a cell membrane-permeable substance.

3. The peptide according to claim 1 , having one or both of properties (i) and (ii) described below:

(i) property of promoting nuclear translocation of PHB2 polypeptide in estrogen receptor-positive cells expressing ERAP1 polypeptide; and

(ii) property of promoting binding of estrogen receptors present in the nucleus and/or on the cell membrane to PHB2 polypeptide in estrogen receptor-positive cells expressing ERAP1 polypeptide.

Assignments (2)
CHANGE OF ENGLISH NAME Recorded Jan 28, 2016
From: THE UNIVERSITY OF TOKUSHIMA
To: TOKUSHIMA UNIVERSITY
Reel/Frame 037630/0710 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 29, 2014
From: KATAGIRI, TOYOMASA; TSUNODA, TAKUYA
To: THE UNIVERSITY OF TOKUSHIMA; ONCOTHERAPY SCIENCE, INC.
Reel/Frame 032073/0159 →