ArticleThe Journal of biological chemistry2016
Biochemical and Spectroscopic Characterization of Highly Stable Photosystem II Supercomplexes from Arabidopsis.
Article in The Journal of biological chemistry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
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10 citing papers in PubMed.
- Optimization of thylakoid solubilization for PSII-LHCII supercomplex isolation from shade-adapted Fittonia albivenis.Photosynthesis research · 2026Article
- Architecture and functional regulation of a plant PSII-LHCII megacomplex.Science advances · 2024Article
- Qualitative and quantitative evaluation of thylakoid complexes separated by Blue Native PAGE.Plant methods · 2022Article
- Article
- Size and Fluorescence Properties of Algal Photosynthetic Antenna Proteins Estimated by Microscopy.International journal of molecular sciences · 2022Article
- Accumulation of geranylgeranylated chlorophylls in the pigment-protein complexes of Arabidopsis thaliana acclimated to green light: effects on the organization of light-harvesting complex II and photosystem II functions.Photosynthesis research · 2021Article
- High-resolution model of Arabidopsis Photosystem II reveals the structural consequences of digitonin-extraction.Scientific reports · 2021Article
- The BBX gene family in Moso bamboo (Phyllostachys edulis): identification, characterization and expression profiles.BMC genomics · 2021Article
- The PsbS protein and low pH are necessary and sufficient to induce quenching in the light-harvesting complex of plants LHCII.Scientific reports · 2021Article
- A novel chloroplast super-complex consisting of the ATP synthase and photosystem I reaction center.PloS one · 2020Article
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Authors and funding
3 authors.
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Abstract
Photosystem II (PSII) is a large membrane supercomplex involved in the first step of oxygenic photosynthesis. It is organized as a dimer, with each monomer consisting of more than 20 subunits as well as several cofactors, including chlorophyll and carotenoid pigments, lipids, and ions. The isolation of stable and homogeneous PSII supercomplexes from plants has been a hindrance for their deep structural and functional characterization. In recent years, purification of complexes with different antenna sizes was achieved with mild detergent solubilization of photosynthetic membranes and fractionation on a sucrose gradient, but these preparations were only stable in the cold for a few hours. In this work, we present an improved protocol to obtain plant PSII supercomplexes that are stable for several hours/days at a wide range of temperatures and can be concentrated without degradation. Biochemical and spectroscopic properties of the purified PSII are presented, as well as a study of the complex solubility in the presence of salts. We also tested the impact of a large panel of detergents on PSII stability and found that very few are able to maintain the integrity of PSII. Such new PSII preparation opens the possibility of performing experiments that require room temperature conditions and/or high protein concentrations, and thus it will allow more detailed investigations into the structure and molecular mechanisms that underlie plant PSII function.
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