Amino acid sequences directed against HER2 and polypeptides comprising the same for the treatment of cancers and/or tumors
The present invention relates to amino acid sequences and Nanobodies that are directed against Epidermal Growth Factor Receptor 2 (HER2), as well as to compounds or constructs, and in particular proteins and polypeptides, that comprise or essentially consist of one or more such amino acid sequences.
1. Isolated amino acid sequence that specifically binds HER2 and inhibits binding of trastuzumab to HER2, and that essentially consists of 4 framework regions (FR1 to FR4, respectively) and 3 complementarity determining regions (CDR1 to CDR3, respectively), in which:
CDR1 is SEQ ID NO:462, and
CDR2 is SEQ ID NO:1012, and
CDR3 is SEQ ID NO:1562.
2. The amino acid sequence according to claim 1 , that is a domain antibody, a single domain antibody, a VHH, a humanized VHH or a camelized VH.
3. The amino acid sequence according to claim 1 , that essentially consists of a VHH, humanized VHH or camelized VH that has at least 80% amino acid identity with at least one of the amino acid sequences of SEQ ID NO's: 1 to 22 or 2051-232, in which for the purposes of determining the degree of amino acid identity, the amino acid residues that form the CDR sequences are disregarded.
4. The amino acid sequence according to claim 3 , wherein one or more of the amino acid residues at positions 11, 37, 44, 45, 47, 83, 84, 103, 104 and 108 according to the Kabat numbering are chosen from:
at position 11: L, M, S, V, W,
at position 37: F, Y, H, I, L, V,
at position 44: G, E, A, D, Q, R, S, L,
at position 45: L, R, C, I, L, P, Q, V,
at position 47: W, L, F, A, G, I, M, R, S, V, Y,
at position 83: R, K, N, E, G, I, M, Q, T,
at position 84: P, A, L, R, S, T, D, V,
at position 103: W, P, R, S,
at position 104: G, D, and
at position 108: Q, L, R.
5. The amino acid sequence according to claim 1 , that is SEQ ID NO:2112.
6. Isolated construct that comprises or essentially consists of one or more amino acid sequences according to claim 1 , and further comprises one or more other groups, residues, moieties or binding units.
7. Construct according to claim 6 , which is a multiparatopic construct, comprising at least one amino acid sequence that binds a first epitope of HER-2 and at least one amino acid sequence that binds a second epitope of HER-2 different from the first epitope.
8. Biparatopic construct according to claim 7 , which can simultaneously bind the pertuzumab binding site on HER2 and to the trastuzumab binding site on HER2.
9. Construct according to claim 6 , wherein said construct specifically binds the trastuzumab binding site on HER2 and specifically binds the pertuzumab binding site on HER2.
10. Construct according to claim 6 , wherein said construct competes with trastuzumab and pertuzumab for binding to HER2 and/or wherein said construct inhibits binding of trastuzumab and pertuzumab to HER2.
11. Construct according to claim 6 , that comprises or consists of one of SEQ ID NO's: 2346 or 2347.
12. Construct according to claim 6 , which has an increased half-life, compared to the corresponding one or more amino acid sequences per se.
13. Construct according to claim 6 that is selected from any of SEQ ID NO's: 2330 and 2335.
14. Composition comprising at least one construct according to claim 6 .
15. Monovalent construct, comprising or essentially consisting of one amino acid sequence according to claim 1 .
16. Composition, comprising at least one amino acid sequence according to claim 1 .