Your browser doesn't support javascript.
loading
Protein-Protein Interactions Induce pH-Dependent and Zeaxanthin-Independent Photoprotection in the Plant Light-Harvesting Complex, LHCII.
Son, Minjung; Moya, Raymundo; Pinnola, Alberta; Bassi, Roberto; Schlau-Cohen, Gabriela S.
Affiliation
  • Son M; Department of Chemistry, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, United States.
  • Moya R; Department of Chemistry, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, United States.
  • Pinnola A; Department of Biology and Biotechnology, University of Pavia, 27100 Pavia, Italy.
  • Bassi R; Department of Biotechnology, University of Verona, 37134 Verona, Italy.
  • Schlau-Cohen GS; Accademia Nazionale di Lincei, 00165 Rome, Italy.
J Am Chem Soc ; 143(42): 17577-17586, 2021 10 27.
Article in En | MEDLINE | ID: mdl-34648708
ABSTRACT
Plants use energy from the sun yet also require protection against the generation of deleterious photoproducts from excess energy. Photoprotection in green plants, known as nonphotochemical quenching (NPQ), involves thermal dissipation of energy and is activated by a series of interrelated factors a pH drop in the lumen, accumulation of the carotenoid zeaxanthin (Zea), and formation of arrays of pigment-containing antenna complexes. However, understanding their individual contributions and their interactions has been challenging, particularly for the antenna arrays, which are difficult to manipulate in vitro. Here, we achieved systematic and discrete control over the array size for the principal antenna complex, light-harvesting complex II, using near-native in vitro membranes called nanodiscs. Each of the factors had a distinct influence on the level of dissipation, which was characterized by measurements of fluorescence quenching and ultrafast chlorophyll-to-carotenoid energy transfer. First, an increase in array size led to a corresponding increase in dissipation; the dramatic changes in the chlorophyll dynamics suggested that this is due to an allosteric conformational change of the protein. Second, a pH drop increased dissipation but exclusively in the presence of protein-protein interactions. Third, no Zea dependence was identified which suggested that Zea regulates a distinct aspect of NPQ. Collectively, these results indicate that each factor provides a separate type of control knob for photoprotection, which likely enables a flexible and tunable response to solar fluctuations.
Subject(s)

Full text: 1 Database: MEDLINE Main subject: Light-Harvesting Protein Complexes / Zeaxanthins Type of study: Prognostic_studies Language: En Year: 2021 Type: Article

Full text: 1 Database: MEDLINE Main subject: Light-Harvesting Protein Complexes / Zeaxanthins Type of study: Prognostic_studies Language: En Year: 2021 Type: Article