Antibody-based targeted therapy in cancer faces a challenge due to uneven antibody distribution in solid tumors, hindering effective drug delivery. We addressed this by developing peptide mimetics with nanomolar-range affinity for Receptor Tyrosine Kinase-Like Orphan Receptor 1 (ROR1) using computational methods. These peptides showed both specific targeting and deep penetration and . Additionally, we created peptide-drug conjugates (PDCs) by linking targeting peptides to toxin drugs via various linkers and enhancing their half-life with fatty side chains for albumin binding. The antitumor candidate displayed exceptional affinity ( = 1.72 × 10 M), internalization efficiency, anticancer potency (IC = 0.015 ± 0.002 μM), and pharmacokinetics ( = 2.6 h), showcasing a rational approach for designing PDCs with favorable tissue distribution and strong tumor penetration.
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http://dx.doi.org/10.1021/acs.jmedchem.4c00511 | DOI Listing |
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