PA1b inhibitor binding to subunits c and e of the vacuolar ATPase reveals its insecticidal mechanism

J Biol Chem. 2014 Jun 6;289(23):16399-408. doi: 10.1074/jbc.M113.541250. Epub 2014 May 2.

Abstract

The vacuolar ATPase (V-ATPase) is a 1MDa transmembrane proton pump that operates via a rotary mechanism fuelled by ATP. Essential for eukaryotic cell homeostasis, it plays central roles in bone remodeling and tumor invasiveness, making it a key therapeutic target. Its importance in arthropod physiology also makes it a promising pesticide target. The major challenge in designing lead compounds against the V-ATPase is its ubiquitous nature, such that any therapeutic must be capable of targeting particular isoforms. Here, we have characterized the binding site on the V-ATPase of pea albumin 1b (PA1b), a small cystine knot protein that shows exquisitely selective inhibition of insect V-ATPases. Electron microscopy shows that PA1b binding occurs across a range of equivalent sites on the c ring of the membrane domain. In the presence of Mg·ATP, PA1b localizes to a single site, distant from subunit a, which is predicted to be the interface for other inhibitors. Photoaffinity labeling studies show radiolabeling of subunits c and e. In addition, weevil resistance to PA1b is correlated with bafilomycin resistance, caused by mutation of subunit c. The data indicate a binding site to which both subunits c and e contribute and inhibition that involves locking the c ring rotor to a static subunit e and not subunit a. This has implications for understanding the V-ATPase mechanism and that of inhibitors with therapeutic or pesticidal potential. It also provides the first evidence for the position of subunit e within the complex.

Keywords: ATPase; Drug Action; Electron Microscopy (EM); Membrane Protein; PA1b; Vacuolar ATPase.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Albumins / antagonists & inhibitors
  • Albumins / metabolism*
  • Base Sequence
  • Benzophenones / metabolism
  • Binding Sites
  • Biotin / metabolism
  • DNA Primers
  • Insecticides / chemistry
  • Insecticides / metabolism*
  • Microscopy, Electron
  • Photoaffinity Labels
  • Pisum sativum / metabolism*
  • Protein Binding
  • Vacuolar Proton-Translocating ATPases / chemistry
  • Vacuolar Proton-Translocating ATPases / metabolism*

Substances

  • Albumins
  • Benzophenones
  • DNA Primers
  • Insecticides
  • Photoaffinity Labels
  • Biotin
  • benzophenone
  • Vacuolar Proton-Translocating ATPases