Enzyme kinetics and inhibition of histone acetyltransferase KAT8

Hannah Wapenaar, Petra E van der Wouden, Matthew R Groves, Dante Rotili, Antonello Mai, Frank J Dekker

Research output: Contribution to journalArticlepeer-review

Abstract

Lysine acetyltransferase 8 (KAT8) is a histone acetyltransferase (HAT) responsible for acetylating lysine 16 on histone H4 (H4K16) and plays a role in cell cycle progression as well as acetylation of the tumor suppressor protein p53. Further studies on its biological function and drug discovery initiatives will benefit from the development of small molecule inhibitors for this enzyme. As a first step towards this aim we investigated the enzyme kinetics of this bi-substrate enzyme. The kinetic experiments indicate a ping-pong mechanism in which the enzyme binds Ac-CoA first, followed by binding of the histone substrate. This mechanism is supported by affinity measurements of both substrates using isothermal titration calorimetry (ITC). Using this information, the KAT8 inhibition of a focused compound collection around the non-selective HAT inhibitor anacardic acid has been investigated. Kinetic studies with anacardic acid were performed, based on which a model for the catalytic activity of KAT8 and the inhibitory action of anacardic acid (AA) was proposed. This enabled the calculation of the inhibition constant Ki of anacardic acid derivatives using an adaptation of the Cheng-Prusoff equation. The results described in this study give insight into the catalytic mechanism of KAT8 and present the first well-characterized small-molecule inhibitors for this HAT.

Original languageEnglish
Pages (from-to)289-96
Number of pages8
JournalEuropean Journal of Medicinal Chemistry
Volume105
DOIs
Publication statusPublished - 13 Nov 2015

Keywords

  • acetyl coenzyme A
  • anacardic acids
  • biocatalysis
  • dose-response relationship
  • enzyme inhibitors
  • histone acetyltransferases
  • histones
  • humans
  • kinetics
  • models in science
  • molecular structure
  • structure-activity relationship
  • molecular
  • metabolism
  • antagonists & inhibitors
  • chemical synthesis
  • drug effects

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