Mechanically interlocked functionalization of monoclonal antibodies

• Published in: Nature communications Vol. 9; no. 1; pp. 1580 - 9
• Main Authors: Bzymek, Krzysztof P., Puckett, James W., Zer, Cindy, Xie, Jun, Ma, Yuelong, King, Jeremy D., Goodstein, Leah H., Avery, Kendra N., Colcher, David, Singh, Gagandeep, Horne, David A., Williams, John C.
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 20-04-2018; Nature Publishing Group; Nature Portfolio
• Subjects: 101/1; 101/58; 13/31; 14/1; 14/34; 14/63; 59/5; 631/61; 631/92; 82/103; Animals; Antibodies, Monoclonal - chemistry; Antibodies, Monoclonal - immunology; Antigens; Azides - chemistry; Binding Sites; Cetuximab - chemistry; Chemical synthesis; Click Chemistry - methods; Crystal structure; Cytotoxins; Drug Carriers - chemistry; Epidermal growth factor; Fab; Female; Fluorescence; Humanities and Social Sciences; Immunoglobulin Fab Fragments - chemistry; Mice; Mice, Inbred NOD; Mice, SCID; Monoclonal antibodies; multidisciplinary; Peptides; Pharmacology; Protein Binding; Radioisotopes; Receptor, ErbB-2 - immunology; Research centers; Science; Science (multidisciplinary); Surface Plasmon Resonance; Trastuzumab - chemistry; Tumors
• ISSN: 2041-1723; 2041-1723
• DOI: 10.1038/s41467-018-03976-5

Because monoclonal antibodies (mAbs) have exceptional specificity and favorable pharmacology, substantial efforts have been made to functionalize them, either with potent cytotoxins, biologics, radionuclides, or fluorescent groups for therapeutic benefit and/or use as theranostic agents. To exploit our recently discovered meditope–Fab interaction as an alternative means to efficiently functionalize mAbs, we used insights from the structure to enhance the affinity and lifetime of the interaction by four orders of magnitude. To further extend the lifetime of the complex, we created a mechanical bond by incorporating an azide on the meditope, threading the azide through the Fab, and using click chemistry to add a steric group. The mechanically interlocked, meditope–Fab complex retains antigen specificity and is capable of imaging tumors in mice. These studies indicate it is possible to “snap” functionality onto mAbs, opening the possibility of rapidly creating unique combinations of mAbs with an array of cytotoxins, biologics, and imaging agents.
Meditope-Fab is a peptide-antibody complex potentially useful for drug delivery and diagnostic, but a short half-life prevents its use in vivo. Here the authors engineer the complex to improve its stability, create functionalized antibodies by click chemistry and use them for in vivo tumor imaging.