Three-dimensional structures of TALL-1 and its cognate receptors and modified proteins and methods related thereto
Disclosed are TALL-1 and TALL-1 receptor protein homologues (agonists and antagonists) designed based on the three-dimensional structure of sTALL-1, eBCMA and eBAFF-R; agonist homologues of APRIL; methods of using wild-type APRIL to inhibit the activity of TALL-1; compositions comprising such homologues, nucleic acid molecules encoding such homologues, and therapeutic methods of using such compounds and compositions. Also disclosed are crystalline complexes of sTALL-1 and sTALL-1 in complex with either BCMA or BAFF-R; models of three-dimensional structures of such crystalline complexes and related structures, methods of drug design using any portion of such structures; methods of design and/or identification of regulatory peptides derived from the such structures; compounds identified by drug design using such structures; and the use of such compounds in therapeutic compositions and methods.
1. A TALL-1 antagonist protein, wherein said protein comprises an amino acid sequence that differs from SEQ ID NO:2, or from an amino acid sequence consisting of positions 134 to 285 of SEQ ID NO:2, by at least one modification in the region connecting β strands D and E that reduces the biological activity of the TALL-1 antagonist as compared to wild-type TALL-1 and by at least a deletion of the following amino acid residues: Val217, His218, Val219, Phe220, Gly221, Asp222, Glu223, and Leu224.
2. A TALL-1 antagonist protein, wherein said protein comprises an amino acid sequence that differs from SEQ ID NO:2, or from an amino acid sequence consisting of positions 134 to 285 of SEQ ID NO:2, by at least one modification in the region connecting β strands D and E that reduces the biological activity of the TALL-1 antagonist as compared to wild-type TALL-1, wherein each of amino acid residues Val217, His218, Val219, Phe220, Gly221, Asp222, Glu223, and Leu224 is either deleted or substituted with a non-natural amino acid.
3. A TALL-1 antagonist protein, wherein said protein comprises an amino acid sequence that differs from SEQ ID NO:2, or from an amino acid sequence consisting of positions 134 to 285 of SEQ ID NO:2, by at least one modification in the region connecting β strands D and E that reduces the biological activity of the TALL-1 antagonist as compared to wild-type TALL-1 and by an additional modification in at least one amino acid residue selected from the group consisting of: Tyr163, Tyr206, Leu211, Arg231, Ile233, Pro264, Arg265, Glu266, Leu200, Leu240, Asp273, Asp275, Glu238 and Asp222; wherein said additional modification increases the binding affinity between the TALL-1 antagonist protein and a TALL-1 receptor, as compared to the binding affinity between wild-type TALL-1 and said TALL-1 receptor.
4. The TALL-1 antagonist protein of claim 3 , wherein the TALL-1receptor is selected from the group consisting of BCMA, BAFF-R and TACI.
5. composition comprising the TALL-1 antagonist protein of claim 3 .
6. A TALL-1 antagonist protein, wherein the TALL-1 antagonist protein comprises an amino acid sequence that differs from SEQ ID NO:2, or from an amino acid sequence consisting of positions 134 to 285 of SEQ ID NO:2, by a modification of at least one amino acid residue that reduces the biological activity of the antagonist protein as compared to a wild-type TALL-1, wherein said amino acid residue is selected from the group consisting of: Gln144, Ile150, Leu169, Phe172, Tyr192, Phe194, Tyr196, Lys216, Val217, His218, Val219, Phe220, Gly221, Asp222, Glu223, Leu224, Val227, Leu229, Tyr246, Ile250, Lys252, Glu254, Leu282, and Leu285; and
wherein the amino acid sequence of the TALL-1 antagonist further differs from SEQ ID NO:2, or from an amino acid sequence consisting of positions 134 to 285 of SEQ ID NO:2, by a modification of at least one amino acid residue that increases the binding affinity between the TALL-1 antagonist protein and a TALL-1 receptor, as compared to the binding affinity between wild-type TALL-1 and said TALL-1 receptor, wherein said amino acid residue is selected from the group consisting of: Tyr163, Tyr206, Leu211, Arg231, Ile233, Pro264, Arg265, Glu266, Leu200, Leu240, Asp273, Asp275, Glu238 and Asp222.
7. A composition comprising the TALL-1 antagonist protein of claim 6 .
8. A TALL-1 antagonist protein, wherein said protein comprises an amino acid sequence that differs from SEQ ID NO:2, or from an amino acid sequence consisting of positions 134 to 285 of SEQ ID NO:2, by at least one modification in the region connecting β strands D and E that reduces the biological activity of the TALL-1 antagonist as compared to wild-type TALL-1 and by a deletion consisting of the following amino acid residues: Val217, His218, Val219, Phe220, Gly221, Asp222, Glu223, and Leu224, wherein said protein retains the ability to bind to a TALL-1 receptor.
9. A TALL-1 antagonist protein, wherein said protein comprises an amino acid sequence that differs from SEQ ID NO:2, or from an amino acid sequence consisting of positions 134 to 285 of SEQ ID NO:2, by at least one modification in the region connecting β strands D and E that reduces the biological activity of the TALL-1 antagonist as compared to wild-type TALL-1, by modifications consisting of: a) a deletion of the following amino acid residues: Val217, His218, Val219, Phe220, Gly221, Asp222, Glu223, and Leu224; and b) a modification in one or more amino acid residues selected from the group consisting of: Tyr163, Tyr206, Leu211, Arg231, Ile233, Pro264, Arg265, Glu266, Leu200, Leu240, Asp273, Asp275 and Glu238, which increases the binding affinity between the TALL-1 antagonist protein and a TALL-1 receptor, as compared to the binding affinity between wild-type TALL-1 and said TALL-1 receptor.
10. A TALL-1 antagonist protein, wherein said protein comprises an amino acid sequence that differs from SEQ ID NO:2, or from an amino acid sequence consisting of positions 134 to 285 of SEQ ID NO:2, by at least one modification that reduces interaction between a first trimer and a second trimer, wherein said first trimer comprises: a) a monomer of said TALL-1 antagonist protein; and b) two monomers selected from the group consisting of: wild-type TALL-1 monomers, said TALL-1 antagonist protein monomers, and mixtures thereof; and wherein said second trimer comprises monomers selected from the group consisting of wild-type TALL-1 monomers, said TALL-1 antagonist protein monomers, and mixtures thereof, wherein said at least one modification consists of: c) a modification of one or more amino acid residues selected from the group consisting of: Ile150, Leu169, Phe172, Tyr192, Lys216, Val217, His218,
Val219, Phe220, Gly221, Asp222, Glu223, Leu224, Val227, Leu229, Ile250, Lys252, and Glu254; and d) a modification of one or more amino acid residues selected from the group consisting of: Tyr163, Tyr206, Leu211, Arg231, Ile233, Pro264, Arg265, Glu266, Leu200, Leu240, Asp273, Asp275, Glu238 and Asp222, which increases the binding affinity between the TALL-1 antagonist protein and a TALL-1 receptor as compared to the binding affinity between wild-type TALL-1 and said TALL-1 receptor.