Substrate Scope for Human Histone Lysine Acetyltransferase KAT8

Int J Mol Sci. 2021 Jan 15;22(2):846. doi: 10.3390/ijms22020846.

Abstract

Biomedically important histone lysine acetyltransferase KAT8 catalyses the acetyl coenzyme A-dependent acetylation of lysine on histone and other proteins. Here, we explore the ability of human KAT8 to catalyse the acetylation of histone H4 peptides possessing lysine and its analogues at position 16 (H4K16). Our synthetic and enzymatic studies on chemically and structurally diverse lysine mimics demonstrate that KAT8 also has a capacity to acetylate selected lysine analogues that possess subtle changes on the side chain and main chain. Overall, this work highlights that KAT8 has a broader substrate scope beyond natural lysine, and contributes to the design of new chemical probes targeting KAT8 and other members of the histone lysine acetyltransferase (KAT) family.

Keywords: acetylation; epigenetics; histone; lysine; posttranslational modifications.

MeSH terms

  • Acetylation
  • Amino Acids / chemistry
  • Catalysis
  • Cell Nucleus / metabolism
  • Epigenesis, Genetic
  • Histone Acetyltransferases / genetics
  • Histone Acetyltransferases / metabolism*
  • Histones / chemistry
  • Humans
  • Kinetics
  • Lysine / chemistry
  • Lysine Acetyltransferases / metabolism*
  • Peptides / chemistry
  • Protein Conformation
  • Protein Processing, Post-Translational
  • Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
  • Substrate Specificity

Substances

  • Amino Acids
  • Histones
  • Peptides
  • Lysine Acetyltransferases
  • Histone Acetyltransferases
  • KAT8 protein, human
  • Lysine