Arylalkalamine N-acetyltransferase-1 acts on a secondary amine in the yellow fever mosquito, Aedes aegypti

FEBS Lett. 2022 Apr;596(8):1081-1091. doi: 10.1002/1873-3468.14316. Epub 2022 Feb 23.

Abstract

Arylalkylamine N-acetyltransferase (aaNAT) in Aedes aegypti is primarily involved in cuticle pigmentation and formation. The reported arylalkylamine substrates are all primary amines. In this study, we report a novel substrate, a secondary amine, of Ae. aegypti aaNAT1. The recombinant aaNAT1 protein exhibited high activity to a secondary amine, epinephrine, which has not been reported for any aaNATs previously. Structure-activity relationship study demonstrated that aaNAT1 has an epinephrine-binding site, and molecular docking and dynamic simulation showed that epinephrine is quite stable in the active cavity. Further functional studies demonstrated that epinephrine affected mosquito fecundity, egg hatching and development. The new biochemical function of aaNAT1 in metabolizing epinephrine could reduce some negative effects of the compound in the mosquito.

Keywords: N-acetyltransferase; epinephrine; functional analysis; haemostasis; mosquito; novel substrate.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetyltransferases
  • Aedes* / genetics
  • Amines
  • Animals
  • Arylamine N-Acetyltransferase
  • Epinephrine
  • Isoenzymes
  • Molecular Docking Simulation
  • Recombinant Proteins
  • Yellow Fever*

Substances

  • Amines
  • Isoenzymes
  • Recombinant Proteins
  • Acetyltransferases
  • Arylamine N-Acetyltransferase
  • N-acetyltransferase 1
  • Epinephrine