High-resolution image of Arabidopsis photosynthesis machine


Using cryoelectron microscopy, Umeå researchers have succeeded in producing a high-resolution image of photosystem II in the plant thale cress. Credit: Wolfgang Schröder, © 2020 andre
Using cryoelectron microscopy, Umeå researchers have succeeded in producing a high-resolution image of photosystem II in the plant thale cress. Credit: Wolfgang Schröder, © 2020 andre
 

For the first time, Umeå researchers have, with the help of cryogenic electron microscopy, succeeded in producing a high-resolution image of photosystem II, the central complex of photosynthesis of the model plant Arabidopsis. The enormous complex is responsible for the vital oxygen production in photosynthesis that once made life possible on our planet. The study is published in Scientific Reports.


Wolfgang Schröder, professor at the Department of Chemistry at Umeå University Sweden, who led the study said, the structure gives us detailed information about the various cofactors such as chlorophyll and the lipid molecules in photosystem II. We have also managed to show exactly where and how detergents bind and affect the stability of the complex.


The plant researcher's experimental rat has for the past 25 years been the plant thale cress/mouse-ear cress Arabidopsis thaliana. The reason for this is that this weed grows rapidly even at our northern latitudes in Sweden and in 2000, researchers succeeded in sequencing all its genes.


At the heart of the photosynthetic process in the Photosystem II complex. It contains almost 30 different proteins and a number of cofactors such as different pigments and metals and it is without any doubt one of the largest complexes in plant chloroplasts. The now published structure from this study has the same high-resolution as the two previous structures obtained from spinach and pea, which for the first time enables a comparison of plants' photosystem II complex with the same level of detail.


I have worked with this complex since I became a Ph.D. student in plant protein chemistry at Lund University in 1983, says Wolfgang Schröder. I remember that as a doctoral student I joked at the coffee break think if you could dive into photosystem II and look around. Today with new technology and my extremely talented doctoral student André Graça and my two fantastic research colleagues Michael Hall and Karina Persson, we have now been able to do this.


The technology that the researchers have used is called cryogenic electron microscopy (Nobel Prize in Chemistry 2017) and it briefly means that biological samples are shot down into liquid ethane (-190 degrees Celsius). Nearly 100,000 two-dimensional EM particle images from random orientations are selected. Using several computational resources, the collection of 2D images can then be used to reconstruct a three-dimensional structure.


Wolfgang Schröder said, additionally, it was extremely exciting to see if our previous biochemical analyzes of the complex were correct. Usually, the privilege of publishing structures with this size and resolution is only possible to larger research teams from different laboratories, as it requires a lot of data, time, and effort. In our case, we are four Umeå researchers within the network Integrated Structural Biology, ISB, who created this structure so it is locally produced research.


Journal Information: André T. Graça et al, High-resolution model of Arabidopsis Photosystem II reveals the structural consequences of digitonin-extraction, Scientific Reports (2021). DOI: 10.1038/s41598-021-94914-x

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