Method for rational mutagenesis of α/βT-cell receptors and correspondingly mutated MDM2-protein specific α/βT-cell receptors

1. An in vitro method for producing a heterodimeric specific wild type- or chimeric T-cell receptor (TCR), said TCR being a human TCR, a murine TCR or a humanized murine TCR, the method comprising:

(a) providing DNA-molecules in joint or separate mutagenesis vector system(s), the DNA-molecules comprising the coding regions for a first and second chain of a TCR, said first and second chain of said TCR interacting at at least one surface in the constant regions of the first and second chains,

(b) mutagenizing the DNA-molecules to produce individual mutated DNA-molecules, wherein the nucleic acid sequence encoding the first chain is mutagenized to encode the first chain comprising a substitution in an amino acid in the at least one surface within the constant region of the first chain, wherein the amino acid interacts with the second chain and the amino acid introduced after mutagenesis in the at least one surface of the first chain provides a sterically projecting group in the constant domain of the first chain and the nucleic acid sequence encoding the second chain is mutagenized to encode the second chain comprising a substitution in an amino acid in the at least one surface within the constant region that of the second chain, wherein the amino acid interacts with the first chain and the amino acid introduced after mutagenesis in the at least one surface of the second chain provides a sterically recessed group in the constant domain of the second chain,

(c) translating the mutated DNA molecules from step (b), such that pairing of the heterodimeric specific first-chain/second-chain TCR being mutated at the at least one surface within the constant region is selectively promoted, and

(d) expressing in vitro the heterodimeric first-chain/second-chain TCR by a T-cell, wherein the first chain and second chain of said TCR interact via the sterically projecting group and the sterically recessed group at said at least one surface located in the constant regions of said first and second chains wherein an amino acid that has been introduced after the mutagenesis of the DNA-molecules that introduces a sterically recessing group compared to the initial sequence is selected from glycine, serine, threonine, valine and alanine, and wherein an amino acid that has been introduced after the mutagenesis of the DNA-molecules that introduces a sterically projecting group compared to the initial sequence is selected from tryptophan, lysine, arginine, phenylalanine, cysteine and tyrosine.

2. The method according to claim 1 , wherein step c) is replaced by the following steps:

(c′) optionally, sub-cloning of the mutated DNA molecules into a suitable transfection-vector system,

(c″) transfection or co-transfection or transduction of at least two of the mutated DNA molecules into a mutant TCR-deficient T-cell, and

(c′″) expression of the heterodimeric first-chain/second-chain TCR in a recombinant T-cell.

3. The method according to claim 1 , wherein step c) is replaced by the following steps:

c′) In vitro-translation or in vivo-translation of at least two of the individual mutated DNA molecules from step (b) and, optionally, subsequent isolation or purification or both isolation and purification of the translated first and second chains, such that the pairing of the heterodimeric specific first-chain/second-chain TCR being mutated at least on one surface is selectively promoted, and

c″) introduction of the mutated specific first-chain/second-chain TCR into a T-cell.

4. method according to claim 3 , wherein the in vivo translation takes place in a host cell.

5. The method according to claim 3 , wherein the introduction takes place by liposome-transfer.

6. The method according to claim 1 , wherein the TCR is an alpha/beta TCR, gamma/delta TCR or a partially humanized TCR.

7. The method according to claim 1 , wherein the amino acids as introduced after the mutagenesis of the DNA-molecules are further suitably chemically modified, in order to thereby introduce a sterically projecting group or a sterically recessing group.

8. The method according to claim 1 , wherein the amino acids as introduced after the mutagenesis of the DNA-molecules directly provide the sterically projecting group or the sterically recessing group.

9. The method according to claim 1 , wherein the amino acids as introduced by the mutagenesis of the DNA-molecules are chosen in such a manner that a mutual exchange of the amino acids on the surfaces of the interacting chains of the TCR is achieved.

10. The method according to claim 1 , wherein at least two surfaces of a TCR-chain are simultaneously subjected to mutagenesis.

11. The method according to claim 1 , wherein the mutagenesis of the TCR-chains also leads to humanization of the TCR.

12. The method according to claim 1 , wherein the alpha- and beta-chains of a mouse-double-minute-2 (MDM2)(81-88)-specific TCR are used as alpha-chain and beta-chain, and wherein the Gly 192 of the constant region of the alpha-chain and the Arg 208 of the constant region of the beta-chain are exchanged by Arg 192 in the constant region of the alpha-chain and by Gly 208 in the constant region of the beta-chain.

13. The method according to claim 12 , wherein simultaneously with or subsequent to the exchanges at positions 192 and 208, additional positions are modified in the chains.

14. The method according to claim 1 , wherein a retroviral vector is used as a transfection system.

15. The method according to claim 1 , wherein said TCR is a murine TCR.

16. The method according to claim 1 , wherein said TCR is a human TCR.