BINDING MOLECULE CONJUGATES
The present invention concerns methods for identifying, producing, and engineering binding molecule conjugates, and to the conjugates produced. In particular, the invention concerns Surrobody conjugates composed of an antibody heavy chain variable domain and a surrogate light chain, wherein the surrogate light chain and/or the antibody heavy chain variable domain is conjugated to a therapeutic or diagnostic agent.
1 - 38 . (canceled)
39 . A binding molecule conjugate comprising a surrogate light chain (SLC) polypeptide having at least one agent linked to an amino acid residue of the SLC polypeptide at a predetermined amino acid position, wherein the amino acid residue is either
(i) normally present in the SLC polypeptide at said amino acid position, or
(ii) introduced into the amino acid sequence of said SLC polypeptide at said amino acid position, wherein the agent is a therapeutic agent, and wherein the therapeutic agent is selected from the group consisting of a maytansinoid, a monomethyl auristatin E (MMAE) and a monomethyl auristatin F (MMAF).
40 - 48 . (canceled)
49 . A Surrobody comprising a surrogate light chain (SLC) having at least one amino acid residue at a predetermined amino acid position for conjugation to an agent, wherein the amino acid residue is located
(i) at position 16 and/or 21 of a mature VpreB1 sequence; and/or
(ii) at one or more positions selected from the group consisting of 60, 74, 78, 79, 85, 91, 110, 123, 131, 133, 166, and 170 of a mature λ5 sequence.
50 . The Surrobody of claim 49 , wherein said amino acid residue is introduced into the amino acid sequence of the SLC polypeptide.
51 . The Surrobody of claim 50 , wherein the amino acid residue is introduced into the amino acid sequence of the SLC polypeptide by a substitution.
52 . The Surrobody of claim 50 or 51 , wherein the introduced amino acid is a cysteine or a lysine.
53 . The Surrobody of claim 51 , wherein the introduced amino acid is a cysteine or a lysine.