A Metabolic Probe-Enabled Strategy Reveals Uptake and Protein Targets of Polyunsaturated Aldehydes in the Diatom Phaeodactylum tricornutum

PLoS One. 2015 Oct 23;10(10):e0140927. doi: 10.1371/journal.pone.0140927. eCollection 2015.

Abstract

Diatoms are unicellular algae of crucial importance as they belong to the main primary producers in aquatic ecosystems. Several diatom species produce polyunsaturated aldehydes (PUAs) that have been made responsible for chemically mediated interactions in the plankton. PUA-effects include chemical defense by reducing the reproductive success of grazing copepods, allelochemical activity by interfering with the growth of competing phytoplankton and cell to cell signaling. We applied a PUA-derived molecular probe, based on the biologically highly active 2,4-decadienal, with the aim to reveal protein targets of PUAs and affected metabolic pathways. By using fluorescence microscopy, we observed a substantial uptake of the PUA probe into cells of the diatom Phaeodactylum tricornutum in comparison to the uptake of a structurally closely related control probe based on a saturated aldehyde. The specific uptake motivated a chemoproteomic approach to generate a qualitative inventory of proteins covalently targeted by the α,β,γ,δ-unsaturated aldehyde structure element. Activity-based protein profiling revealed selective covalent modification of target proteins by the PUA probe. Analysis of the labeled proteins gave insights into putative affected molecular functions and biological processes such as photosynthesis including ATP generation and catalytic activity in the Calvin cycle or the pentose phosphate pathway. The mechanism of action of PUAs involves covalent reactions with proteins that may result in protein dysfunction and interference of involved pathways.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphate / biosynthesis
  • Aldehydes / chemistry*
  • Algal Proteins / analysis*
  • Algal Proteins / chemistry
  • Algal Proteins / metabolism
  • Animals
  • Chromatography, Liquid
  • Copepoda / physiology
  • Diatoms / chemistry*
  • Diatoms / metabolism
  • Electrophoresis, Gel, Two-Dimensional
  • Food Chain
  • Molecular Probes / chemistry*
  • Molecular Sequence Annotation
  • Pentose Phosphate Pathway / physiology
  • Photosynthesis / physiology
  • Phytoplankton / physiology
  • Proteome / analysis*
  • Proteome / chemistry
  • Proteome / metabolism
  • Staining and Labeling / methods
  • Tandem Mass Spectrometry

Substances

  • Aldehydes
  • Algal Proteins
  • Molecular Probes
  • Proteome
  • 2,4-decadienal
  • Adenosine Triphosphate

Grants and funding

Support was provided by the Deutsche Forschungsgemeinschaft, German Research Foundation (DFG) and Studienstiftung des deutschen Volkes.