1. Academic Validation
  2. Exploration of macrocyclic peptide binders to the extracellular CRD domain of human receptor tyrosine kinase-like orphan receptor 1 (ROR1)

Exploration of macrocyclic peptide binders to the extracellular CRD domain of human receptor tyrosine kinase-like orphan receptor 1 (ROR1)

  • Bioorg Med Chem Lett. 2023 Dec 13:98:129589. doi: 10.1016/j.bmcl.2023.129589.
Jennifer X Qiao 1 Mark R Witmer 2 Ving Lee 3 Tammy C Wang 3 Patrick C Reid 4 Yuki Arioka 4 Glen Farr 5 Melissa Hill-Drzewi 5 Liang Schweizer 5 Aaron Yamniuk 2 Lin Cheng 2 Bozena Abramczyk 2 Martin Corbett 2 Deepa Calambur 2 Nicolas Szapiel 2 Rolf Ryseck 2 Paul Ponath 6 Michael A Poss 3 Percy Carter 3
Affiliations

Affiliations

  • 1 Discovery Chemistry, Princeton, NJ 08543, United States. Electronic address: [email protected].
  • 2 Molecular Discovery Technology, Princeton, NJ 08543, United States.
  • 3 Discovery Chemistry, Princeton, NJ 08543, United States.
  • 4 PeptiDream 3-25-23 Tonomachi, Kawasaki-Ku, Kawasaki-Shi, Kanagawa 210-0821, Japan.
  • 5 Leads Discovery & Optimization, Princeton, NJ 08543, United States.
  • 6 Discovery Biology, Bristol-Myers Squibb, Princeton, NJ 08543, United States.
Abstract

Elevated levels of receptor tyrosine kinase-like orphan receptor 1 (RORl) expression are observed in multiple hematological and solid tumors, but not in most of the healthy adult tissues, identifying ROR1 as an attractive target for tumor-specific therapy. Herein we will describe the discovery of macrocyclic Peptides as binders of the extracellular Cysteine-Rich Domain (CRD) of human ROR1 via mRNA in vitro selection technology using the PDPS platform, followed by exploration of sidechain SAR of parent macrocycle Peptides, fluorescently labeled analogs, and a Peptide Drug Conjugate (PDC). The parent macrocyclic Peptides represented by Compound 1 and Compound 14 displayed nanomolar cell-based binding to ROR1 and relatively good internalization in 786-O and MDA-MB-231 tumor cell lines. However, these Peptides were not observed to induce Apoptosis in Mia PaCa-2 cells, a model pancreatic tumor cell line with a relatively low level of cell surface expression of ROR1.

Keywords

Extracellular CRD domain; Human receptor tyrosine kinase-like orphan receptor 1 (ROR1); Macrocyclic peptides; Peptide Drug Conjugate (PDC); Peptide synthesis and SAR; mRNA in vitro selection technology.

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