Modified antibody and radioactive metal-labelled antibody
Described is a labeling technique which can facilitate the metabolism in the liver after administration to patients without the reduction in the antibody function, thereby reducing accumulation of radionuclides in an organ such as the liver, and a modified antibody containing an IgG antibody and an IgG-binding peptide bound to the IgG antibody. The IgG-binding peptide has an amino acid sequence consisting of 13 to 17 amino acid residues, such as GPDCAYH(Xaa1)GELVWCTFH (SEQ ID NO: 2) wherein Xaa1 represents a lysine residue, a cysteine residue, an aspartic acid residue, a glutamic acid residue, 2-aminosuberic acid, or diaminopropionic acid, and a compound represented by the following formula (II-1) is linked at a position of the lysine residue via a modification linker to the N terminus of the IgG-binding peptide.
1. A modified antibody comprising
an IgG antibody, and
an IgG-binding peptide bound to the IgG antibody, wherein
the IgG-binding peptide comprises an amino acid sequence represented by the following formula (I) which consists of 13 to 17 amino acid residues, and further comprises a compound represented by the following formula (I-1) that is linked at a position of the lysine residue thereof via a modification linker to the N-terminus of the amino acid sequence represented by formula (I),
(X 1-3 )-C-(X 2 )-H-(Xaa1)-G-(Xaa2)-L-V-W-C-(X 1-3 ) (I) (SEQ ID NO: 6),
wherein
each X independently represents an amino acid residue other than cysteine,
C represents a cysteine residue,
H represents a histidine residue,
Xaa1 represents a lysine residue, a cysteine residue, an aspartic acid residue, a glutamic acid residue, 2-aminosuberic acid, or diaminopropionic acid,
G represents a glycine residue,
Xaa2 represents a glutamic acid residue, a glutamine residue, or an asparagine residue,
L represents a leucine residue,
V represents a valine residue, and
W represents a tryptophan residue, and
the two cysteine residues may be disulfide-bonded or bound to each other via a linker, and the C terminus may be amidated,
and
wherein n is 0 or 1.
2. The modified antibody according to claim 1 , wherein a binding site between the lysine residue of the compound represented by the above formula (II-1) and the modification linker is formed by a click reaction between a dibenzocyclooctyne (DBCO) group and an azido group.
3. The modified antibody according to claim 2 , wherein
the modification linker is represented by the following formula (III):
L 1 -L 2 -L 3 (III)
wherein
L 1 represents a polyethylene glycol linker bound to the N terminus of the amino acid sequence represented by formula (I),
L 2 represents an amino acid sequence consisting of 0 or more and 5 or less amino acid residues, and
L 3 represents a group having a DBCO group at the terminus,
and wherein
an alkyl azide group having 1 to 10 carbon atoms is introduced to the lysine residue of the compound represented by the above formula (II-1) so that a binding site between the lysine residue and the modification linker is formed by a click reaction.
4. The modified antibody according to claim 1 , wherein
the IgG-binding peptide represented by the above formula (I) has the following amino acid sequence:
GPDCAYHKGELVWCTFH (SEQ ID NO: 2)
wherein the two cysteine residues may be disulfide-bonded, and the C terminus may be amidated.
5. The modified antibody according to claim 4 , wherein
in the above formula (III), L 2 represents a cysteine residue, and L 3 is formed by reacting DBCO-maleimide represented by the following formula (IV):
with the cysteine residue of L 2 .
6. A radioactive metal-labeled antibody comprising the modified antibody according to claim 1 , to which a radioactive metal is coordinated.
7. A radiopharmaceutical comprising the radioactive metal-labeled antibody according to claim 6 .
8. A compound comprising a compound represented by the following formula (II), to which a polypeptide to be bound to a target molecule is bound, or a salt thereof:
wherein n is 0 or 1, R 1 and R 2 both represent a hydrogen atom, or one of R 1 and R 2 represents a hydrogen atom and the other represents a group represented by CO(CH 2 ) m N 3 where m is an integer of 1 to 10, or both form a maleimide group or isothiocyanate group together with the nitrogen atom,
or a salt thereof.
9. A compound represented by the following formula (II):
wherein n is 0 or 1, one of R and R 2 represents a hydrogen atom and the other represents a group represented by CO(CH 2 ) m N 3 where m is an integer 1 to 10,
to which a polypeptide to be bound to a target molecule is bound, or a salt thereof, wherein
the polypeptide is a modified IgG-binding peptide comprising:
an IgG-binding peptide comprising an amino acid sequence represented by the following formula (I) which consists of 13 to 17 amino acid residues,
and
a modification linker represented by the following formula (III) that is bound to the N terminus of the IgG-binding peptide,
(X 1-3 )-C-(X 2 )-H-(Xaa1)-G-(Xaa2)-L-V-W-C-(X 1-3 ) (I) (SEQ ID NO: 6),
wherein
each X independently represents an amino acid residue other than cysteine,
C represents a cysteine residue,
H represents a histidine residue,
Xaa1 represents a lysine residue, a cysteine residue, an aspartic acid residue, a glutamic acid residue, 2-aminosuberic acid, or diaminopropionic acid,
G represents a glycine residue,
Xaa2 represents a glutamic acid residue, a glutamine residue, or an asparagine residue,
L represents a leucine residue,
V represents a valine residue, and
W represents a tryptophan residue, and
the two cysteine residues may be disulfide-bonded or bound to each other via a linker, and the C terminus may be amidated,
and
L 1 -L 2 -L 3 (III)
wherein
L 1 represents a polyethylene glycol linker bound to the N terminus of the IgG-binding peptide,
L 2 represents an amino acid sequence consisting of 0 or more and 5 or less amino acid residues, and
L 3 represents a group having a DBCO group at the terminus,
and
wherein the compound is bound to the polypeptide by a click reaction between the azide group in the formula (II) and the DBCO group in the formula (III).
10. A compound represented by the following formula (II):
wherein n is 0 or 1, one of R 1 and R 2 represents a hydrogen atom and the other represents a group represented by CO(CH 2 ) m N 3 where m is an integer 1 to 10,
to which a polypeptide to be bound to a target molecule is bound, or a salt thereof, wherein
the polypeptide is an IgG antibody to which a modified IgG-binding peptide is bound, wherein the modified IgG-binding peptide comprises:
an IgG-binding peptide comprising an amino acid sequence represented by the following formula (I) which consists of 13 to 17 amino acid residues,
and
a modification linker represented by the following formula (III) that is bound to the N terminus of the IgG-binding peptide,
(X 1-3 )-C-(X 2 )-H-(Xaa1)-G-(Xaa2)-L-V-W-C-(X 1-3 ) (I) (SEQ ID NO: 6),
wherein
each X independently represents an amino acid residue other than cysteine,
C represents a cysteine residue,
H represents a histidine residue,
Xaa1 represents a lysine residue, a cysteine residue, an aspartic acid residue, a glutamic acid residue, 2-aminosuberic acid, or diaminopropionic acid,
G represents a glycine residue,
Xaa2 represents a glutamic acid residue, a glutamine residue, or an asparagine residue,
L represents a leucine residue,
V represents a valine residue, and
W represents a tryptophan residue, and
the two cysteine residues may be disulfide-bonded or bound to each other via a linker, and the C terminus may be amidated,
and
L 1 -L 2 -L 3 (III)
wherein
L 1 represents a polyethylene glycol linker bound to the N terminus of the IgG-binding peptide,
L 2 represents an amino acid sequence consisting of 0 or more and 5 or less amino acid residues, and
L 3 represents a group having a DBCO group at the terminus,
and
wherein the compound is bound to the polypeptide by a click reaction between the azide group in the formula (II) and the DBCO group in the formula (III).