Biparatopic polypeptides antagonizing Wnt signaling in tumor cells
The invention provides novel biparatopic LRP5/LRP6 cross-reactive binding polypeptides, and more specifically novel biparatopic LRP5/LRP6 cross-reactive immunoglobulin single variable domain constructs which can inhibit Wnt signaling pathways. The invention also relates to specific sequences of such polypeptides, methods of their production, and methods of using them, including methods of treatment of diseases such as cancer.
1. A cross-reactive biparatopic polypeptide which specifically binds to an epitope of the human low-density receptor-like protein 5 (LRP5) as well as an epitope of the human low-density receptor-like protein 6 (LRP6), comprising
a first immunoglobulin single variable domain wherein binding of said first single immunoglobulin domain is capable of inhibiting the Wnt1 signaling pathway comprising the CDR sequences:
CDR1:
(= SEQ ID NO: 4)
SYAMG
CDR2:
(= SEQ ID NO: 5)
AIRRSGRRTYYADSVKG
CDR3:
(= SEQ ID NO: 6)
ARRVRSSTRYNTGTWWWEY;
and
a second immunoglobulin single variable domain wherein binding of said second single immunoglobulin domain is capable of inhibiting the Wnt3a signaling pathway comprising the CDR sequences:
CDR1:
(= SEQ ID NO: 13)
SYAMG
CDR2:
(= SEQ ID NO: 14)
AISWRSGSTYYADSVKG
CDR3:
(= SEQ ID NO: 15)
DPRGYGVAYVSAYYEY.
2. The cross-reactive biparatopic polypeptide of claim 1 , wherein said immunoglobulin single variable domains are VHH domains.
3. The cross-reactive biparatopic polypeptide of claim 1 , wherein
said first immunoglobulin single variable domain has the amino acid sequence as shown in SEQ ID NO:20 and
said second immunoglobulin single variable domain has the amino acid sequence as shown in SEQ ID NO:23.
4. The cross-reactive biparatopic polypeptide of claim 1 , wherein said first and said second immunoglobulin single variable domains are covalently linked by a linker peptide, wherein said linker peptide comprises or consists of a third immunoglobulin single variable domain.
5. The cross-reactive biparatopic polypeptide of claim 1 , wherein the polypeptide additionally includes a half-life extending moiety, wherein said half-life extending moiety is covalently linked to said polypeptide and is an albumin binding immunoglobulin single variable domain comprising the Alb11 domain, defined by SEQ ID NO:24.
6. A cross-reactive biparatopic polypeptide comprising or consisting of SEQ ID NO:26.
7. A nucleic acid molecule encoding a cross-reactive biparatopic polypeptide according to claim 1 .
8. An expression vector comprising the nucleic acid of claim 7 .
9. A host cell carrying an expression vector according to claim 8 .
10. A method of manufacturing a polypeptide according to claim 1 , comprising the steps of
culturing a host cell under conditions that allow expression of a polypeptide according to claim 1 ; and
recovering said polypeptide.
11. The method of claim 10 , additionally comprising the step of
purifying said polypeptide.
12. A pharmaceutical composition comprising (i) as the active ingredient, the cross-reactive biparatopic LRP5 and LRP6 binding polypeptide according to claim 1 capable of antagonizing the Wnt1 and Wnt-3a signaling/activation pathways, and (ii) a pharmaceutically acceptable carrier, and optionally (iii) a diluent, excipient, adjuvant and/or stabilizer.
13. The cross-reactive biparatopic polypeptide of claim 2 , wherein said immunoglobulin single variable domains are humanized VHH domains.