Single-Molecule Force Measurement Guides the Design of Multivalent Ligands with Picomolar Affinity

Zhen Yang, Sheng Jiang, Feng Li, Yatao Qiu, Jianhua Gu, Roderic I. Pettigrew, Mauro Ferrari, Dale J. Hamilton, Zheng Li

Research output: Contribution to journalArticle

4 Scopus citations

Abstract

Interaction of multiple entities and receptors, or multivalency is widely applied to achieve high affinity ligands for diagnostic and therapeutic purposes. However, lack of knowledge on receptor distribution in living subjects remains a challenge for rational structure design. Herein, we develop a force measurement platform to probe the distribution and separation of the cell surface vascular endothelial growth factor receptors (VEGFR) in live cells, and use this to assess the geometry of appropriate linkers for distinct multivalent binding modes. A tetravalent lead ZD-4, which was developed from an antitumor drug ZD6474 (Vandetanib) with combined hybrid binding effects, yielded a 2000-fold improvement in the binding affinity to VEGFR with IC 50 value of 25 pm. We confirmed the improved affinity by the associated increase of tumor uptake in the VEGFR-targeting positron emission tomography (PET) imaging using U87 tumor xenograft mouse model.

Original languageEnglish (US)
Pages (from-to)5272-5276
Number of pages5
JournalAngewandte Chemie - International Edition
Volume58
Issue number16
DOIs
StatePublished - Apr 8 2019

Keywords

  • PET imaging
  • atomic force microscopy
  • ligand design
  • multivalency
  • tumor targeting

ASJC Scopus subject areas

  • Catalysis
  • Chemistry(all)

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