Totally synthetic affinity reagents
AssigneeThe University of North Carolina at Chapel Hill
InventorsBrian K. Kay, Nils B. Adey
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AssigneeThe University of North Carolina at Chapel Hill
InventorsBrian K. Kay, Nils B. Adey
Estimating the term…
A novel method for producing novel and/or improved heterofunctional binding fusion proteins termed Totally Synthetic Affinity Reagents (TSARs) is disclosed. TSARs are concatenated heterofunctional proteins, polypeptides or peptides comprising at least two functional regions: a binding domain with affinity for a ligand and a second effector peptide portion that is chemically or biologically active. In one embodiment, the heterofunctional proteins, polypeptides or peptides further comprise a linker peptide portion between the binding domain and the second active peptide portion. The linker peptide can be either susceptible or not susceptible to cleavage by enzymatic or chemical means. Novel and/or improved heterofunctional binding reagents as well as methods for using the reagents for a variety of in vitro and in vivo applications are also disclosed.
A peptide which binds specifically to the 7E11-C5 monoclonal antibody produced by hybridoma cell line ATCC HB-10494 and having an amino acid sequence selected from the group consisting of SEQ ID NOs. 22-31.
A peptide of up to 200 amino acids which binds specifically to the 7E11-C5 monoclonal antibody produced by hybridoma cell line ATCC HB-10494 and having an amino acid sequence comprising the consensus sequence Met (Trp/Tyr/His/Ile) Xaa Xaa Leu (His/Arg), wherein Xaa is any amino acid.
A peptide which binds specifically to the 7E11-C5 monoclonal antibody produced by hybridoma cell line ATCC HB-10494 and having an amino acid sequence consisting of the consensus sequence Met (Trp/Tyr/His/Ile) Xaa Xaa Leu (His/Arg), wherein Xaa is any amino acid.
Dependencies are inferred from the claim text.