(R)-PFI-2 Analogues as Substrates and Inhibitors of Histone Lysine Methyltransferase SETD7

Miriam Porzberg, Danny Lenstra, Eddy Damen, Richard Blaauw, Floris Rutjes, Anita Wegert, Jasmin Mecinović*

*Corresponding author for this work

Research output: Contribution to journalJournal articleResearchpeer-review

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Abstract

(R)-PFI-2 is a histone substrate-competitive inhibitor of the human histone lysine monomethyltransferase SETD7. Aimed at developing potent inhibitors of SETD7 that can also act as small molecule substrates, we replaced the pyrrolidine ring of (R)-PFI-2 with several side chains bearing nucleophilic functional groups. We explored the inhibitory activity of 20 novel (R)-PFI-2 analogues, and found that the most potent analogue has a hydroxyethyl side chain (7). SETD7's ability to catalyse methylation of (R)-PFI-2-based small molecules was evaluated by mass spectrometric assays, and we observed efficient methylation of analogues bearing lysine mimicking nucleophilic amines. The optimal side chain was found to be an aminoethyl group (1), which was surprisingly also dimethylated by SETD7. The work demonstrates that small molecules can act as both substrates and inhibitors of biomedically important SETD7.

Original languageEnglish
Article numbere202300457
JournalChemMedChem
Volume18
Issue number23
Number of pages14
ISSN1860-7179
DOIs
Publication statusPublished - 1. Dec 2023

Keywords

  • (R)-PFI-2
  • SETD7
  • epigenetics
  • histone lysine methyltransferase
  • structure-activity relationships
  • Histone-Lysine N-Methyltransferase
  • Lysine
  • Humans
  • Histones
  • Pyrrolidines/pharmacology

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