Proteotypic profiling of LHCI from Chlamydomonas reinhardtii provides new insights into structure and function of the complex

Proteomics. 2009 Jan;9(2):398-408. doi: 10.1002/pmic.200700620.

Abstract

We used isotope dilution MS to measure the stoichiometry of light-harvesting complex I (LHCI) proteins with the photosystem I (PSI) core complex in the green alga Chlamydomonas reinhardtii. Proteotypic peptides served as quantitative markers for each of the nine gene products (Lhca1-9) and for PSI subunits. The quantitative data revealed that the LHCI antenna of C. reinhardtii contains about 7.5 +/- 1.4 subunits. It further demonstrated that the thylakoid LHCI population is heterogeneously composed and that several lhca gene products are not present in 1:1 stoichiometries with PSI. When compared with vascular plants, LHCI of C. reinhardtii possesses a lower proportion of proteins potentially contributing to far-red fluorescence emission. In general, the strategy presented is universally applicable for exploring subunit stoichiometries within the C. reinhardtii proteome.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Arabidopsis / chemistry
  • Arabidopsis / metabolism
  • Carbon Isotopes / chemistry
  • Chlamydomonas reinhardtii / chemistry
  • Chlamydomonas reinhardtii / metabolism*
  • Gene Expression Regulation, Plant / physiology
  • Isotope Labeling
  • Light-Harvesting Protein Complexes / analysis*
  • Light-Harvesting Protein Complexes / metabolism
  • Membrane Proteins / analysis*
  • Membrane Proteins / metabolism
  • Molecular Sequence Data
  • Photosystem I Protein Complex / analysis*
  • Photosystem I Protein Complex / metabolism
  • Plant Proteins / analysis
  • Plant Proteins / metabolism
  • Proteomics / methods*
  • Thylakoids / chemistry
  • Thylakoids / metabolism

Substances

  • Carbon Isotopes
  • Light-Harvesting Protein Complexes
  • Membrane Proteins
  • Photosystem I Protein Complex
  • Plant Proteins